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COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH HUMAN RESOURCE DEVELOPMENT GROUP CSIR COMPLEX, PUSA, NEW DELHI - 110 012

SHANTI SWARUP BHATNAGAR PRIZE PROFORMA FOR UPDATING NOMINATION

(Original+4 copies must be forwarded latest by 31 March 2015; digital photograph & softcopy of duly filled proforma of the nominee on CD/DVD preferably in MS-

WORD are also required)

1. Name of the nominee in Full

(Both in English and Hindi)

: Dr. B.V. Subba Reddy

2. (a) Date and place of birth (Enclosed certificate of the age duly attested) (b) Nationality (c) Gender (d) Age as on 31st Dec 2014 :

: : :

10th June 1970, Kadapa Indian Male 44 years 6 months 21 days

3. Address with Telephone / Mobile / Fax/e-mail: (a) Official

Senior Principal Scientist

Natural Product Chemistry, CSIR-Indian Institute of Chemical Technology Tarnaka, Hyderabad – 500 607 ( : (Off.) 91-40- 27193535 FAX: 91-40-27160512

E-mail:[email protected]/ [email protected]

(b) Residential

301, Versha Apart. Bapuji Nagar Nacharam, Hyderabad – 500 076 ( : (Res): +91-40-27170287 Mobile: 9494540587

4. Discipline under which to be considered (only one to be marked/ encircled)

: (i) Biological (ii) Chemical (iii) Earth, Atmosphere, Ocean and Planetary (iv) Engineering (v) Mathematical (vi) Medical and (vii) Physical Sciences

5. Nominee's field of specialization

: Asymmetric Synthesis using Chiral Ligands and Organocatalysis; Tandem Prins Cyclization; Metal Catalyzed Cycloaddition of Diazocarbonyl compounds; Natural Products Synthesis employing Chiral Sources such as Carbohydrates and Ellman's Chiral Auxiliary.

2

6. Academic Qualifications (Bachelor's Degree onwards):

Title of the Ph D thesis : Synthesis of camptothecin analogues, luotonin A, linopiridine and novel synthetic methodologies

Name of the guide : Dr. J. S. Yadav

7. Date of joining the Institution (Designation & Scale)

: June, 2006 Scientist EI (Rs. 12000)

8. Positions held earlier (in chronological order)

S. No. Period Place of Employment Designation Scale of pay

1 1996-1998 IICT, Hyderabad JRF

2 1998-2001 IICT, Hyderabad SRF

3 2001-2003 IICT, Hyderabad Research Associate

4 2004-2006 Department of Chemical Biology, Harvard University, USA

Post Doctoral Fellow with Prof. E. J. Corey

5 June 2006- May 2009

IICT, Hyderabad Senior Scientist 12000-15600

Qualification

Subject(s)

University

Year of Passing

Division

B.Sc. Geology, Physics & Chemistry

S.V. University, Tirupati, AP

1991 First

M.Sc. Organic Chemistry S.K.University, Anantapur, AP

1994 First

Ph.D Organic Synthesis IICT (Osmania University, Hyderabad) AP

2003 -

Post Doctoral Fellow Synthetic Organic/ Medicinal Chemistry, Prof. E. J. Corey, Nobel Laureate

Harvard University, USA

2004-2006

Six Publications

3

6 June 2009 -Feb 2011

IICT, Hyderabad Principal Scientist 37400-67000 GP 8700

7 2011-till date

IICT, Hyderabad Senior Principal Scientist

37400-67000 GP 8700

8 Feb 2011-Aug 2011

Max-Planck Institute of Molecular Physiology, Dortmund, Germany

Alexander von Humboldt Fellowship (AvH)

-

9. Details of CSIR Fellowship/Associateship held, if any or from other sources/ agencies

(indicate dates of joining & leaving):

v CSIR JRF (1996-1998) v CSIR SRF (1998-2001)

10. (a) Significant foreign assignments:

S. No. Period of visit Institute/country visited

Purpose of visit

1 May 2004 May 2006 Harvard University, USA

Post-Doctoral Fellow

2 Aug 2008

Nov 2008 National Institute of Material Science, Japan

Indo-Japan Collaborative Project

3 May 2010 July 2010 National Institute of Material Science, Japan

Indo-Japan Collaborative Project

4 Feb 2011 Aug 2011 Max-Planck Institute of Molecular Physiology, Dortmund, Germany

Alexander von Humboldt Fellowship (AvH)

(b) Total time spent abroad during last 5 years: 8 months (2 months in 2010 and 6

months in 2011)

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11. Names and complete addresses of 10 Distinguished Scientists including 5 in India in the area (as possible referees):

Name Correspondence address with email ID Broad area of specialization

Prof. S. Chandrasekaran

Honorary Professor IISc, Banglore. E-mail: [email protected] Tel: 91-80-2293-2404/2403 Fax: 91-80-2360-0529

Organic Chemistry

Prof. Javed Iqbal

Director Institute of Life Sciences, University of Hyderabad Campus Gachibowli, Hyderabad-500 046 Tel: +91 40 66571500, Fax: +91 40 66571581, E-mail: [email protected]

Organic Chemistry

Prof. D. Basavaiah

School of Chemistry, University of Hyderabad 158, Hyderabad - 500 046, INDIA Tel: +91-(0)40-23134814 (Office), Fax: +91-(0)40-23012460, E-mail: [email protected]

Organic Chemistry

Prof. Dr. Oliver Reiser Institut für Organische Chemie Universität Regensburg Universitätsstr. 31 93053 Regensburg Tel.: Int-49-(0)941-943-4631 (4630) Fax.: Int-49-(0)941-943-4121 E-mail: [email protected]

Organic Chemistry/Asymmetric Synthesis

Prof. V. K. Singh

Director Indian Institute of Science Education & Research, Bhopal Transit Campus: ITI Campus (Gas Rahat) Building Govindpura, Bhopal - 460 023 Tel: +91-755-2601096 Fax: +91-755-4092392 E-mail: [email protected]

Organic Chemistry/ Asymmetric Synthesis

5

Prof. Rene Gree

Directeur de Recherche CNRS Université de Rennes 1 Sciences Chimiques de Rennes, CNRS UMR 6226, Avenue du Général Lecler 35042 RENNES Cedex, France Fax: +33 2 23 23 69 78 E-mail: [email protected]

Organic/Green Chemistry

Dr A. Ajayaghosh

Outstanding Scientist, CSIR – National Institute for Interdisciplinary Science and Technology. E-mail: [email protected] Phone(Off) : 0471-2515306 Mobile : +91-9446059059

Photosciences and Photonics

Prof. E. J. Corey

Department of Chemistry and Chemical Biology, 12 Oxford Street, Cambridge, MA 02138, USA. Tel: 617-495-4033; Fax: 617-495-0376. E-mail: [email protected]

Organic Chemistry/ Asymmetric Synthesis

Prof. H. Waldmann

Prof. Scott A Snyder

Max Planck Institute of Molecular Physiology, Dept. of Chemical Biology, Otto-Hahn-Strasse 11 44227 Dortmund, Germany Tel: ++49 (0) 231 / 133 - 2400 Fax: ++49 (0) 231 / 133 - 2499 E-mail: [email protected] Department of Chemistry, Havemeyer Hall, Mail Code 3129 3000 Broadway, New York E-mail:[email protected] Tel: 212-854-3817 Fax: 212-932-1289

Organic Chemistry/ Chemical Biology

Organic Chemistry/Natural Product Synthesis

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12 (a) Significant contributions to science and/or technology development by the nominee based on the work done in India during most part of last 5 years (in about 500 words). Specific reference is to be made to research papers published and patents taken in this context:

Dr. B. V. Subba Reddy has proven his ability as a outstanding researcher since 2006. From the last 5 years, Dr Reddy has been actively working on asymmetric synthesis using transition metal catalysis and organocatalysis, tandem Prins cyclization, metal catalyzed cycloaddition reactions of α-diazocarbonyl compounds, natural products synthesis using various chiral sources such as sugars and Ellman's chiral auxiliary. In the area of asymmetric synthesis, he was primarily involved in the design, synthesis and application of sugar based chiral ligands such as bis-oxazolines (developed as alternatives to D-amino acid derived bis-oxazolines) for the enantioselective C-C bond formation reactions such as Mukaiyama Michael reaction (Advanced Synthesis & Catalysis, 2013, 355, 383), Friedel-Crafts alkylation (Org. Biomol. Chem. 2012, 10, 4731). Recently, he has reported organocatalytic (quinine-squaramide) enantioselective addition of diphenyl phosphite to ketimines derived from isatins for the synthesis of chiral α-aminophosphonates (Org. Biomol. Chem. 2014, 12, 1595). He is the first to develop sugar based chiral thioureas for the enantioselective Michael addition reactions (RSC Advances 2013, 3, 930; RSC Advances 2013, 3, 8756; RSC Advances 2014, 4, 9107; RSC Advances 2014, 4, 42299).

Besides asymmetric catalysis, he has developed a new concept of tandem cyclization of oxo-carbenium ions by olefin tethered with nucleophiles. He is the first to develop 'tandem Prins cyclizations' such as Prins/Friedel-Crafts cyclization (J. Org. Chem. 2011, 76, 7677; Eur. J. Org. Chem. 2013, 1993; J. Org. Chem. 2013, 78, 8161), Prins/bicyclization (Org. Biomol. Chem. 2012, 10, 6562; J. Org. Chem. 2013, 78, 6303; Org. Biomol. Chem. 2012, 10, 1349; Org. Biomol. Chem. 2014, 12, 4754; J. Org. Chem. 2014, 79, 2716), Prins/ene cyclization (Org. Biomol. Chem. 2015, 13, 2669; Eur. J. Org. Chem. 2015, in press), Prins/pinacol reaction (Org. Biomol. Chem. 2014, 12, 7257), Prins/Wagner/Ritter reaction (Org. Biomol. Chem. 2015, 13, in press), Prins/spirocyclization (Organic Lett. 2014, 16, 6267; Eur. J. Org. Chem. 2014, 4234; RSC Advances, 2014, 16739; J. Org. Chem. 2014, 79, 2289; J. Org. Chem. 2015, 80, 653) and Prins bicyclization (Eur. J. Org. Chem. 2015, in press and Org. Biomol. Chem. 2015, 13, in press) using homoallylic substrates with tethered nucleophiles.

In addition to tandem Prins strategy, he has been working on transition metal catalyzed cycloaddition reactions of diazocarbonyl compounds for the synthesis of highly substituted pyrroles and indoles (Organic Letters 2013, 15, 464) and for the synthesis of spirooxindolyl oxazolidines/pyrrolines (Organic Letters 2013, 15, 1512), dispirooxindoles (Eur. J. Org. Chem. 2015. DOI: 10.1002/ejoc.201500002), spirooxindolyl furocoumarins (Tetrahedron 2014, 70, 8148) and oxindole derived α-alkoxy-β-amino acids (Eur. J. Org. Chem. 2014. 2221). He has also been working on Gold catalysis to generate the spirooxindole (Eur. J. Org. Chem., 2014, 3313) and tetrahydropyrido[4,3-b]indole scaffolds (J. Org. Chem. 2012, 77, 11355).

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In addition to above contributions, he was involved in the total synthesis of biologically active molecules such as (-)-Dihydrotetrabenazine, (-)-Crispine, (-)-Harmicine, Solefinacin and Almorexant using Ellman's chiral auxiliary.

At the same time, he was actively involved in industrial sponsored projects for the development novel color changing dyes as sensory cues for liquid soap and anti-bacterial agents for tooth paste and mouth wash as personel hygiene. The synthetic routes for making novel anti-bacterial agents are patented jointly by CSIR-IICT and Colgate-Palmolive Company. The titles of patents are "Process for making magnolol derivatives (US patent 8,519,197 B2)." "Process for producing propyl isopropylmagnolol (PCT/IN2013/000049)." The synthetic process developed for the synthesis of honokiol has been published (Tetrahedron Letters, 2014, 55, 1049). In recognition of his industrial contributions, he has recently been awarded NASI-Reliance Industries Platinum Jubilee Award (2014). Dr Reddy has always been in the forefront as a leader for guiding Ph.D students to promote higher education. 12(b) Summarise the most significant work of the nominee on which the recommendation

is based (in 50 words): On the study of the effect of sugar moiety in enancing the enantioselectivity in thiourea catalysis, the discovery of cooperative catalysis in tandem cyclization, the effect of acidity of the catalyst in tunning the reactivity of sulfur and oxygen, unusual spirocyclization of N-aryl tethered acryloyl amide and novel reactions of diazocompounds.

12(c) Impact of the contributions in the field concerned, basic or applied: From the last 5 years, Dr Reddy has made significant contributions in asymmetric synthesis using transition metal catalysis and organocatalysis. In the area of organocatalysis, he newly desinged and synthesized a novel series of sugar-Cinchona, sugar-indane amine and rosin–indane amine bifunctional thiourea catalysts for enantioselective C-C bond forming reactions to generate biological relevant scaffolds. He reported for the first time, the role of sugar moiety in enhancing the enantioselectivity in thiourea catalysis (RSC Advances 2013, 3, 930; RSC Advances 2013, 3, 8756; RSC Advances 2014, 4, 9107; RSC Advances 2014, 4, 42299. In addition to this, he has reported organocatalytic (quinine-squaramide) enantioselective addition of diphenyl phosphite to ketimines derived from isatins for the synthesis of chiral α-aminophosphonates (Org. Biomol. Chem. 2014, 12, 1595). Besides organocatalysis, he was also involved in the development of sugar based chiral ligands such as bis-oxazolines (as alternatives to D-amino acid derived bis-oxazolines) for the enantioselective C-C bond formation reactions such as Mukaiyama Michael reaction (Advanced Synthesis & Catalysis, 2013, 355, 383), Friedel-Crafts alkylation (Org. Biomol. Chem. 2012, 10, 4731).

8

Asymmetric

Organo Catalysisee up to 99%

O

OOH

TBSO

R

*NO2

N

NO HN

OAc

AcOAcO

OAc HS

HN

O

O

OO

Ph

*

OHOEt

O

ee up to 99%

H

NH

S

HN N

O

O

OH

RNO2

ee up to 99%

*

N

NO HN

OAc

AcOAcO OAc HS

HN

O

H

HN S

NH

N

NO2

R

O

O

*

ee up to 96%

N

BocHN

O

Me

PO

OPh

OPhHN

N

MeO

N

HN

OO

CF3

F3C

ee up to 98%

RSC Adv 2013, 3, 8756.

RSC Adv 2014, 4, 42299. Org.Biomol Chem 2014, 12, 1595.

RSC Adv 2013, 3, 930.

RSC Adv 2014, 4, 9107

Asymmetric

Organometallics

NOH

Ph Ph

NOH

NO2

ee up to 86%

R

ONO

NH

N N

OOO O

OAcO OAcOO O

ee up to 97%

O Ph ONO

N NO O

ee up to 97%

N N

O OO O

OAcAcO AcO OAc

AcO OAc

OHNO2

ee up to 99%

Tetrahedron Asym. 2011, 22, 1169

Advanced Synthesis & Catalysis, 2013, 355, 383

Tetrahedron Asym. 2011, 22, 530

Org.Biomol Chem 2012, 10, 4731

R

He has also developed Proline based trifunctional organocatalyst for enantioselective Aldol, Michael and Mannich reactions (Tetrahedron Asymmetry 2011, 22, 881) and 2-picolinyl-L-diphenylprolinol-Cu(II) complex for asymmetric Henry reaction (Tetrahedron Asymmetry 2011, 22, 530) and sugar-bis-oxazoline-Cu(II) complex for enantioselective nitro-Aldol reaction (Tetrahedron Asymmetry 2011, 22, 1169).

In addition to asymmetric catalysis, Dr Reddy has been aggressively working on Prins and related cyclizations to produce a large number of biologically relevant oxa-, aza-, and thia-cycles. He has developed a new concept of tandem cyclization of oxo-carbenium ion by a nucleophile tethered olefin. This tandem process generally

proceeds through a concerted reaction pathway to produce a novel class of fused or briged bicycles. It is a highly diastereoselective process, which generates three to four contiguous

9

stereocenters in a single step. This method is very useful and highly convergent in the total synthesis of biologically active natural products especially tetrahydropyran and tetrahydrofuran containing molecules. His group has successfully demonstrated its synthetic verstality in natural products synthesis, for example, diarylheptanoids (anti-cancer), sesamin (fat reduction supplement), polyrhacitide (morning sickness, pulmonary diseases) and etc. This cascade strategy is extremely useful to constuct biological relevant spirocycles (psychotic disorders). The scope of this process is widely exemplefied in the synthesis of spiromorpholines, spirooxindoles, spiroisoquinolines, spiropyrrolidines, spiropiperidines, spirotetrahydrocarbolines and spiroisobenzofuran derivatives. Besides spirocycles, fused bicyclic systems like oxa-aza, oxa-thia-, aza-thia- dioxa-, diaza-, and dithia-bicycles through Prins, aza-Prins- and thia-Prins cyclizations. He is the first to develop 'tandem Prins cyclizations' such as (i) Prins/Friedel-Crafts cyclization (J. Org. Chem. 2011, 76, 7677; Eur. J. Org. Chem. 2013, 1993; J. Org. Chem. 2013, 78, 8161). (ii) Prins/bicyclization (Org. Biomol. Chem. 2012, 10, 6562; J. Org. Chem. 2013, 78, 6303; Org. Biomol. Chem. 2012, 10, 1349; Org. Biomol. Chem. 2014, 12, 4754; J. Org. Chem. 2014, 79, 2716). (iii) Prins/ene cyclization (Org. Biomol. Chem. 2015, 13, 2669; Eur. J. Org. Chem. 2015, in press). (iv) Prins/pinacol rearrangement (Org. Biomol. Chem. 2014, 12, 7257), Prins/Wagner/Ritter reaction (Org. Biomol. Chem. 2015, 13, in press). (v) Prins/spirocyclization (Organic Lett. 2014, 16, 6267; Eur. J. Org. Chem. 2014, 4234; RSC Advances, 2014, 16739; J. Org. Chem. 2014, 79, 2289; J. Org. Chem. 2015, 80, 653). (vi) domino Prins cyclization (Eur. J. Org. Chem. 2015, in press and Org. Biomol. Chem. 2015, 13, in press) from aldehydes and homoallylic substrates tethered with nucleophiles.

Besides asymmetric and Prins reaction, Dr. Reddy has successfully explored the synthetic application of a-diazoketones to generate a variety of biologically active heterocycles. In particular, he has developed transition metal catalyzed synthesis of highly substituted pyrroles and indoles (Organic Letters 2013, 15, 464); synthesis of

spirooxindolyl oxazolidines/pyrrolines

(Organic Letters 2013, 15, 1512); synthesis of dispirooxindoles (Eur. J.

Org. Chem. 2015. DOI: 10.1002/ejoc.201500002), synthesis of spirooxindolyl furocoumarins

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(Tetrahedron 2014, 70, 8148); synthesis of oxindole derived α-alkoxy-β-amino acids (Eur. J. Org. Chem. 2014. 2221); synthesis of spiro(oxindolyl)oxazinones and spiro(oxindolyl)-β-lactams from a-diazocarbonyl compounds (Tetrahedron Letters 2012, 53, 2396; Tetrahedron Letters 2012, 53, 3416).

He has been working on gold catalysis to generate the spirooxindoles (Eur. J. Org. Chem., 2014, 3313) and tetrahydropyrido[4,3-b]indoles (J. Org. Chem. 2012, 77, 11355) and sugar annulated furan derivatives (Tetrahedron 2015, 71, DOI:10.1016/j.tet.2015.02.089).

In addition to above contributions, he was actively involved in the total synthesis of biologically active molecules such as (-)-dihydrotetrabenazine (Tetrahedron Letters 2012, 53, 6916), almorexant (Tetrahedron Letters, 2014, 55, 3157),

(-)-crispine/(-)-salsolidine (Tetrahedron Letters 2013, 54, 4228), (-)-harmicine (Organic Biomolecular Chemistry under revsion), solefinacin Synthesis-Stuttgart 2014, 46, 2794) and using Ellman's chiral auxiliary. Many of these molecules are being used for the treatment of various diseases such as neurodegenerative genetic disoder (chorea), stress, depression, insomnia, and contraction of overactive bladder (to avoid involuntary excretion of urine).

In addition to chiral sulfinamide chemistry, he has reported the total synthesis of biologically active natural products such as Attenol A (Tetrahedron Lett. 2013, 54, 5781); Phomonol (Helvetica Chim. Acta, 2014, 1326); Seimatopolide A (Tetrahedron Lett. 2012, 53, 5749); Xyolide (Tetrahedron Lett. 2013, 54, 5758); Cleistenolide (Tetrahedron Lett. 2011, 52, 2306); Phomolide (Synlett, 2014, 501); Anamarine (Tetrahedron Letters, 2014, 55, 1398); (+)-8-Ethylnorlobelol (Tetrahedron Lett. 2013, 54, 4960); Deoxoprosophylline (Tetrahedron Lett. 2012, 53, 4551); Hapalosin (Synlett, 2013, 1415); Penaresidine A (Tetrahedron Lett. 2014, 55, 49); L-783,290 (Tetrahedron Lett. 2014, 55, 5420); PF1163A (Tetrahedron Lett. 2014, 55, 1519).

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Piperidine alkaloids

Tetrahedron Letters, 2012, 53, 4551.

NH

HO

10 Deoxoprosophylline

Synlett, 2013, 1415.

HO

OH

NH

Penaresidine A

OH

9


N

MeO

MeO

O

NH

CF3AlmorexantTetrahedron Letters, 2014, 55, 3157.

N

MeO

MeO

OH

H

(-)-Dihydrotetrabenazine

Tetrahedron Letters,2012, 53, 6916.

N

MeO

MeOH

(-)-Crispine


OH HN

(+)-8-ethylnorlobelol


Polyketides

OH

MeO

O

OH

OOH

O

L-783,290

Tetrahedron Lett. 2014, 55, 5420.

O

OOH

OH

5

O

O

O

HO

Xyolide

O

OHHO OH

O(

)7

O

O

OAc OAcOBz

O

O

OHOMeHO

O O

HOOH OH

O

OHOH O

Attenol A

Tetrahedron Lett. 2013, 54 5758.



Seimatopolide A

Cleistenolide


PhomolideSynlett,

2014, 501.

PhomonolHelvetica Chim. Acta, 2014, 1326

N O

O N

Solifenacin

H

Synthesis, 2014, 46, 2794

ON

OHO

O

OOH

PF1163A

Tetrahedron Letters 2014, 1519.

HO

Hapalosin

O

O

OAc

OAc

OAc

OAc

Anamarine

Tetrahedron Letters, 2014, 1398–1401

O

OO

O

N

O

OH

( )5

He has developed a novel strategy through an intramolecular azomethine cycloaddition for the construction of trisubstituted pyrrole ring system, which is a core structure of Ternatusine A.

At the same time, he was actively involved in industrial sponsored projects for the development novel color changing dyes as sensory cues for liquid soap and anti-bacterial agents for tooth paste, mouth wash, moisturising creams (skin

care) and anti-dandruff shampoo (hair care) as personel hygiene. The synthetic routes developed by him for making novel anti-bacterial agents are patented jointly by CSIR-IICT and Colgate-Palmolive Company. The titles of the patents are "Process for making magnolol derivatives (US patent 8,519,197B2)." "Process for producing propyl isomagnolol (PCT/ IN2013/ 000049). "The synthetic process developed for the synthesis of honokiol has been published (Tetrahedron Letters, 2014, 55, 1049). Besides this, he is also involved in large scale synthesis of hinokitiol, which is being used in personal care products such as hair tonics (hair restoration and hair growth and sterilizing agent for hair cosmetics), tooth paste (for tooth growth, germs kill, elimination of bad breath) and skin cleanser (to prevent skin scaling, dandruff, acne or atopic dermatitis). Hinokitiol is a natural bactericidal agent.

Recently, he is involved in the development of novel synthetic route for natural shellac, which has enormous applications in surface coatings such as wood polish and nail polish.

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Presently, he is working on the development of industrially viable process for poly(ally)guanidine, which is used in Gum Tissue Graft Surgery. In recognition of his industrial contributions, he has received the NASI-Reliance Industries Platinum Jubilee Award (2014). Therefore the nominee has strong background in asymmetric synthesis, synthetic methodologies and total synthesis of natural products.

Dr Reddy has always been in the forefront as a leader for guiding Ph.D students to promote higher education.

Some of the publications are highlighted in Organic Chemistry Portal

Organic Chemistry Highligts:

1. The Prins cyclization is a powerful approach for the construction of oxygen-containing heterocycles. B. V. Subba Reddy at the Indian Institute of Technology has reported (Tetrahedron Lett. 2012, 53, 3100. DOI:10.1016/j.tetlet.2012.04.029) an approach to 2,6-dioxabicyclo[3.2.1]octanes 2 by way of a tandem Prins reaction / intramolecular acetalization of the diol 1 and a variety of aldehydes. Monday, January 14, 2013 by Tristan H. Lambert, Columbia University.

iBu OO

+iBu 15 mol% p-TSA

5 mol% Sc(OTf)3

H

O

OH

21

OH

2. B. V. Subba Reddy of the Indian Institute of Chemical Technology, Hyderabad took advantage (Tetrahedron Lett. 2011, 52, 5926. DOI: 10.1016/j.tetlet.2011.08.098) of the directing ability of the amide to effect selective orthoacetoxylation of 17. Monday, June 25, 2012, by Douglass F.Taber, University of Delaware.

O

NH

O Ph17

PhI(OAc)2

Pd cat

O

NH

O PhOAc

18

3. Alkaloid Synthesis: Penaresidin A (3), isolated from the Okinawan marine sponge Penares sp., is a potent activator of actomyosin ATPase. B.V. Subba Reddy of the Indian Institute of Chemical Technology prepared (Tetrahedron Lett. 2014, 55, 49. DOI:10.1016/j.tetlet.2013.10.095) the azetidine ring of 3 by mesylation of the hydroxy sulfonamide 2 followed by cyclization. Monday, November 24, 2014,by Douglass F. Taber, University of Delaware.

OBn

NHTs

OBn

OH OTBDPS1. MsCl

2. NaHN

Ts

1 2

BnO

OBn

OTBDPS

NH

HO

OH

HO3

Penaresidin A

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4. The dihydroisocoumarin 7-Desmethoxyfusarentin (34) was isolated from the insect pathogenic fungus Ophiocordyceps communis. B. V. Subba Reddy prepared (Tetrahedron Lett. 2012, 53, 4051. DOI: 10.1016/j.tetlet.2012.05.059) the arene of 33 by the Alder-Rickert reaction of 31 with the Birch reduction product 32. Monday, June 17, 2013by Douglass F. Taber, University of Delaware.

TBSO

OTBS

CO2CH3

31

OCH3H3CO

32 TBSO

OTBS

H3CO OCH3

CO2CH3O OH

OOH

H3CO34

7-Desmethoxyfusarentin

33

Synfacts Highlights

The following articles are highlighted in Synfacts v “Synthesis of heterobicycles by intramolecular aza-Prins cyclization” [Sc(OTf)3 Catalyzed an

intramolecular aza-Prins cyclization for the synthesis of heterobicycles” Tetrahedron Letters 2010, 51, 3412] has been selected by SYNFACTS for its important insights.

v “Synthesis of α-Aminophosphonates with Nano Fe3O4” [Nano Fe3O4 as Magnetically Recyclable Catalyst for the Synthesis of α-Aminophosphonates in Solvent-Free Conditions” Tetrahedron Letters 2011, 52, 1359] has been selected by SYNFACTS for its important insights.

v “Cerium(III)-Catalyzed Synthesis of N-Arylpyrrolidines” [Cerium(III) Chloride Heptahydrate-Lithium Iodide: A Novel Reagent System for the Synthesis of N-Arylpyrrolidines” Synthesis 2009, 3448] has been selected by SYNFACTS for its important insights.

v “Diaryl Amines via Addition of Aryl Cuprates to Aryl Azides” [Addition of Aryl Cuprates to Azides: A Novel Approach for the Synthesis of Unsymmetrical Diaryl Amines” [Tetrahedron Letters 2009, 50, 6642] has been selected by SYNFACTS for its important insights.

v “Chitosan-SO3H: an efficient, biodegradable, and recyclable solid acid for the synthesis of quinoline derivatives via Friedlander annulation'' [Tetrahedron Letters, 2013, 54, 5767] has been selected by SYNFACTS for its important insights.

v "Synthesis of Spiromorpholinotetrahydropyrans through a Prins Bicyclization" [Prins cascade cyclization for the synthesis of 1,9-dioxa-4-azaspiro[5.5]undecane derivatives: Journal of Organic Chemistry 2014, 79, 2289] has been selected by SYNFACTS for its important insights.

v "Oxa-versus Thia-Selectivity in the Prins Cyclization" [Tuning the reactivity of oxygen/sulfur by acidity of the catalyst in Prins cyclization: oxa- vs thia-selectivity: Journal of Organic Chemistry 2014, 79, 2716] has been selected by SYNFACTS for its important insights.

v "Synthesis of 3,4-Disubstituted Hexahydro-1H-furo [3,4-c] pyran Derivatives" [InBr3-Catalyzed Stereoselective Synthesis of 3,4-Disubstituted Hexahydro-1H-furo[3,4-c]pyran Derivatives: Tetrahedron Letters, 2014, 55, 4110] has been selected by SYNFACTS for its important insights.

v "Enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone and 1,3-dicarbonyls to β-nitroalkenes catalyzed by a novel bifunctional rosin-indane amine thiourea catalyst'' [Advanced Synthesis and Catalysis 2013, 355, 383] has been selected by SYNFACTS for its important insights.

14

CHEMINFORM Highlights

The following articles are highlighted in CHEMINFORM

v "Three-component, one-pot synthesis of hexahydroazepino[3,4-b]indole and tetrahydro-1H-pyrido[3,4-b]indole derivatives and evaluation of their cytotoxicity" [Bioorganic & Med. Chem. Lett., 2014, 24, 4501] has been selected by CHEMINFORM for its important insights.

v "Tandem Prins/Pinacol Reaction for the Synthesis of Oxaspiro[4.5]decan-1-one Scaffolds" [Org. Biomol. Chem., 2014, 15, 7257] has been selected by CHEMINFORM for its important insights.

v "Stereoselective Total Synthesis of Oplopandiol, Oploxyne A, and Oploxyne B" [Tetrahedron Letters, 2014, 55, 4590] has been selected by CHEMINFORM for its important insights.

v "Acetal-Initiated Prins Bicyclization for the Synthesis of Hexahydrofuro-[3,4-c] furan Lignans and Octahydropyrano[3,4-c]pyran Derivatives" [Org. Biomol. Chem., 2014, 12, 4754] has been selected by CHEMINFORM for its important insights.

v "Rh2(OAc)4-Catalyzed Substrate Selective [4+2]/[2+2] Cycloaddition of Acylketenes: A Highly Chemo- and Regioselective Synthesis of Spiro(oxindolyl)oxazinones and β-Lactams" [Tetrahedron Letters, 2012, 53, 2396] has been selected by CHEMINFORM for its important insights.

v "Stereoselective Total Synthesis of (+)-Boronolide,(+)-Anamarine, 8-epi-Spicegerolide" [Tetrahedron Letters, 2014, 55, 1398] has been selected by CHEMINFORM for its important insights.

Special featured articles

v “Oxidative Prins and Prins/Friedel–Crafts cyclizations for the stereoselective synthesis of

dioxabicycles and hexahydro-1H-benzo[f]isochromenes via the benzylic C–H activation” published in Organic and Biomolecular Chemistry 2012, 10, 1349 has received Top 10 accessed articles from Organic & Biomolecular Chemistry (Royal Society of Chemistry)

v Top 10 Cited Author 2011-2012 to the work published in Tetrahedron Asymmetry 2011, 22, 530, from Elsevier Science, UK.

v “Honey Derivatized Au and Ag Nanoparticles and Evaluation of Its Antimicrobial Activity” published in Journal of Nanoscience and Nanotechnology, 2011, 11, 6995, was highlighted in Life Science Weekly, November 1st, 2011. http://www.newsrx.com/newsletters/Life-Science-Weekly/2011-11-01/25110120113472LS.html

v “Gold Nanoparticles Embedded in a Mesoporous Carbon Nitride Stabilizer for Highly Efficient Three-Component Coupling Reaction” published in Angew. Chem. Int. Engl. Ed., 2010, 49, 5961 and was highlighted in Nature India. http://www.nature.com/nindia/2010/100812/full/nindia.2010.111.html

v “[Bmim]BF4: A novel reaction media for the synthesis of b-aminoalcohols” published in Tetrahedron Letters 2003, 44, 1047 has received most cited paper 2003-2006 Award from Elsevier Science.

15

12(d) Places where work of last 5 years has been referred/cited in Journals, Books, Reviews: (See Annexure-I).

(i) Citations of papers published from 2010-15: No of Papers No of Citations

Number of papers published in 2010: 53 (Citations in journals/books 1190) Number of papers published in 2011: 35 (Citations in journals/books 1200) Number of papers published in 2012: 44 (Citations in journals/books 1280) Number of papers published in 2013: 37 (Citations in journals/books 1210) Number of papers published in 2014: 49 (Citations in journals/books 1350) Number of papers published in 2015: 12 (including articles in press) Total number of publications from 2010-15: 230 (ii) Citations of total papers published from 1997-2015: Dr Reddy has received as 16th most productive scientist in India as reflected in the publication output of Scopus International database for the years 1996-2006. Also received 5th rank in average citations per paper and 8th rank in H-index. He has a publication record of about 617 papers in a short span (1997-2015), which received over 12319 citations, and an h-index of 53 with 19.97 average citations per paper. As per web of science publication data, he stands second highest in terms of citations in the area of Oranic Chemistry. No of Papers 1997-2015 No of Citations 1997-2015

16

12(e) Names of the industries in which the technology (ies) has (have) been used (give the production figures of products):

v Colgate-Palmolive Company has adopted two of his technologies entitled (a) Processes for making magnolol derivatives (US patent 8,519,197 B2) (b) Process for producing propyl isopropylmagnolol (PCT/IN2013/000049) to produce novel anti-bacterial agents so as to replace triclosan from tooth paste

v Fluorescein Dyes have been deveped for Colgate-Palmolive Company for use in Hand-Wash (Liquid Aquarium Soap).

v One of his papers entitled “Metal triflates catalyzed efficient synthesis of 3,4-dihydro-2H-1-benzopyrans” published in J. Chem. Soc., Perkin Trans 1 2002, 165 has received significant attention from Gilead Science Inc, (Organic Process Research and Development, 2007, 11, 972) and GlaxoSmithKline (Organic Letters 2008, 10, 1103) to prepare hexahydrofuro[2,3-b]furan-3-ol core of Darunavir (HIV-protease inhibitor TMC114).

13. Have the achievements already been recognised by Awards by any learned body. If so, the name of the body, award and the year of award may be given. (A copy of the citation is enclosed) Industry Awards:

v 2014-NASI-Reliance Industries Platinum Jubilee Award v 2009-AVRA Young Scientist Award by AVRA Research Foundation

Academic Awards: v 2010-CRSI Young Scientist by Chemical Research Society of India v 2008-Scopus Young Scientist Award by Elsevier Science, The Netherlands v 1995-Y.S. Raja Reddy GOLD MEDAL by Sri Krishnadevaraya University, Anantapur

Honours: v 2010-Alexander von Humboldt Fellowship by AvH Research Foundation v 2009-IICT Roll of Honor Award by IICT v 2007-Best Performance Award for publishing highest number of research papers 52 with

a total impact factor 124.5. v 2001-Best Performance Award for publishing highest number of research papers 35 with

a total impact factor 78.2; Average I F= 2.25 v 2001-Director's Special Award for oustanding effort in publishing highest number of

research papers 24 with a total impact factor 50.4.

Number of publications: 617 Sum of the Times Cited [?] : 12319

Sum of Times Cited without self-citations [?] : 10727 h-index [?] : 53

(iii) Citations of the nominee’s publications in text books and book chapters from 2008 onwards:

(See Annexure-I). v Cited 51 times in March's Advanced Organic Chemisry, 7th Edition

17

14. Is the nominee a fellow of the Indian National Science Academy / Indian Academy of Sciences / National Academy of Sciences / others (give details):

v 2013-Fellow of National Academy of Sciences

v 2014-Fellow of Andhra Pradesh Academy of Sciences

15. Has the nominee delivered invited lecture(s) in India abroad and/ or chaired any scientific international Conference/Symposium (give details):

National:

S. No. Conference Title Place Year 1. Ionic Liquids as Green Solvents for

Organic Transformations National Science Day at IICT Feb 2003

2. Green Chemistry using Sustainable Solvents and Reagents

First Indo-French Conference, at IICT

July 2007

3. Green Protocols in Asymmetric Synthesis using Immobilized Chiral Ru and Rh Complexes

Indo-Hungarian Workshop, at Raman Institute, Banglore

Sep 2009

4. Green Protocols using Vegetables (whole or Intact Plant cells) as a Source of Enzymes

Indo-French Conference at Kochin

Nov 2009

5. The use of HBF4.OEt2 and SelectfluorÔ for Organic Synthesis

Fisrt Indian International Symposium on Fluorine Chemistry (IISFC), at NDCC II, New Delhi

Feb 2012

6. “Development of Novel Methodologies and their Application for the Natural Product Synthesis”

Organic Synthesis for Human Wellbeing at IICT

Aug 2010

7. “Development of Green Methods utilizing Sustainable Solvents/Reagents

Sri Vikrama Simhapuri Uiniversity, Nellore, India

Sep 2010

8. Prins Cyclization as a Powerful Tool in Organic Synthesis

Chemistry and Chemical Biology of Natural Products, IICT

Aug 2012

9. Development of Novel Synthetic Routes for Industrially Important Products

NASI-84th Symposium on Desert Science

Dec 2014

18

International: (Details of plenary/invited talks and sessions chaired in last 3 years have been given)

S. No. Conference Title Place Year 1. Green Protocols using Solid Acids/Solid

Supported Reagents National Institute of Materials Science, Tsukuba, Japan

July 2010

2. Multi-component Reactions for New Chemical Entities

Universite de Rouen, France June 2011

3. Green Protocols using Sustainable Solvents and Reagents

ESPCI in Paris, France July 2011

4. Prins Cyclization as a Versatile Synthetic tool for Tetrahydropyran Scaffolds

Université de Rennes 1, France

June 2011

5. Metal Catalyzed Transformations for New Chemical Entities

University of Caen, France June 2011

6. Prins Cyclization as a Versatile Synthetic tool for Tetrahydropyran Scaffolds.

University of Nantes, France July 2011

7. Metal Catalyzed Transformations for New Chemical Entities

Department of Pharmacy and Medicine, Université de Rennes 1, France.

July 2011

8. Green Protocols using Sustainable Solvents and Reagents

University of Regensburg Germany

Aug 2011

9. Synthesis and Biological Evaluation of Heliannane Inspired Compound Collections

Max-Planck Institute of Molecular Physiology, Dortmund, Germany

Aug 2011

10. Synthesis of Novel Functionalized Piperidines and Bicyclic Scaffolds via Aza-Prins and Prins Cyclizations (Poster)

French Chemical Society meeting in Palaiseau near Paris, France

Sep 2010

16(a)* List of nominee's 10 most significant publications: (Annexure 16a) 1. Enantioselective Friedel–Crafts Alkylation of Indoles with 2-Enoylpyridine-N-oxides Catalyzed

by glucoBOX-Cu(II) Complex: Organic & Biomol. Chem. 2012, 10, 4731. Jimil George, B. V. Subba Reddy 2. Enantioselective Mukaiyama-Michael Reaction of Silyl Enol Ethers to 2-Enoylpyridine-N-

Oxides Catalyzed by Cu(II)-bis(oxazoline) Complex: Advanced Synthesis & Catalysis, 2013, 355, 383.

Jimil George, B. V. Subba Reddy

3. First Example of Quinine-squaramide Catalyzed Enantioselective Addition of Diphenyl Phosphite to Ketimines Derived from Isatins: Org. Biomol. Chem. 2014, 12, 1595.

Jimil George, B. Sridhar, B. V. Subba Reddy

4. Stereoselective Synthesis of Hexahydro-1H-pyrano- and Thiopyrano[3,4-c]quinoline Derivatives through a Prins Cascade Strategy: J. Org. Chem., 2013, 78. 8161.

19

B. V. Subba Reddy, M. Durgaprasad, B. Sridhar

5. Stereoselective Synthesis of Spiro[tetrahydropyran-3,3'-oxindole] Derivatives employing Prins Cascade Strategy: Organic Letters, 2014, 16, 6267.

B. V. Subba Reddy, V. Swathi, Manisha Swain, Manika Pal Bhadra, B. Sridhar, D. Satyanarayana, B. Jagadeesh

6. Prins Cascade Cyclization for the Synthesis of 1,9-Dioxa-4-azaspiro[5.5]undecane Derivatives: J. Org. Chem. 2014, 79, 2289.

B. V. Subba Reddy, Durgaprasad Medaboina, B. Sridhar, S. Kiran Kumar

7. Stereoselective Synthesis of Hexahydro-1H-spiro[isoquinoline-4,4'-pyran] Scaffolds through Prins Cascade Process: J. Org. Chem. 2015, 80, 653.


8. Stereoselective Synthesis of Highly Functionalized Dispirooxindoles through [3+2] Cycloaddition of Carbonyl Ylides with 3-Arylidene Oxindoles: Eur. J. Org. Chem. 2015, 2038.

B. V. Subba Reddy, G. Karthik, T. Rajasekaran, B. Sridhar 9. Dual Behavior of Isatin-based Cyclic Ketimines with Dicarbomethoxy Carbene: Expedient

Synthesis of Highly Functionalized Spirooxindolyl Oxazolidines and Pyrrolines: Organic Letters, 2013, 15, 1512.

T. Rajasekaran, G. Karthik, B. Sridhar, B. V. Subba Reddy 10. Cu(OTf)2-Catalyzed Synthesis of 2,3-Disubstituted Indoles and 2,4,5-Trisubstituted Pyrroles

from α-Diazoketones: Organic Letters 2013, 15, 464. B. V. Subba Reddy, M. Ramana Reddy, Y. Gopal Rao, J. S. Yadav, B. Sridhar 11. Gold-Catalyzed Domino Cycloisomerization/Pictet–Spengler Reaction of 2-(4-Aminobut-1-yn-

1-yl)anilines with Aldehydes: Synthesis of Tetrahydropyrido[4,3-b]indole Scaffolds: J. Org. Chemistry 2012, 77, 11355.

B. V. Subba Reddy, Manisha Swain, S. M. Reddy, J. S. Yadav, B. Sridhar

16(b)* List of nominee's 5 most significant publications during the last 5 years: : (Annexure 16b, two reprints)

S. No. Author Title Journal Year Vol Page nos.

1 B.V.Subba Reddy et al

Enantioselective Mukaiyama-Michael reaction of silyl enol ethers to 2-enoylpyridine-N-oxides catalyzed by Cu(II)-bis(oxazoline) complex

Advanced Synthesis and Catalysis

2013 355

383

2 B.V.Subba Reddy et al

Thia-Prins bicyclization approach for the stereoselective synthesis of dithia- and azathia-bicycles

Journal of Organic Chemistry

2013 78 6303

3 B. V. Subba Reddy et al

Stereoselective synthesis of spiro[tetrahydropyran-3,3'-oxindole] derivatives employing

Organic Letters

2014, 16 6267

20

Prins Cascade Strategy


Tuning the Reactivity of Oxygen/ Sulfur by Acidity of the Catalyst in Prins cyclization: Oxa- vs Thia- Selectivity


2014 79 2716


Stereoselective Synthesis of Hexahydro-1H-spiro[isoquinoline-4,4 '-pyran] Scaffolds through Prins Cascade Process


2015 80 653

16(c)* List of nominee's 5 most significant publications from out of the work done in India during the last five years:

As same as the above

16(d)* Complete list of publications in standard refereed journals (See Annexure IV):

Journal name No of

Papers Journal name Number

of papers J. Am. Chem. Soc.

1

Tetrahedron Letters

229

Angew. Chem. Int. Ed. Engl. 2 Tetrahedron 14 Organic Letters 8 Synthesis 81 Journal of Organic Chemistry 13 Synlett 58 Advanced Synthesis and Catalysis 9 Chemistry Letters 35 Green Chemistry 7 Synthetic Communications 21 Journal of Chemical Research 6 J. Mol. Cat. A: Chemical 20 JCS Perkin Transactions 5 New Journal of Chemistry 10 Eur. J. Org. Chemistry 16 Catalysis Communications 6 Chemical Communications 2 Letters in Organic Chemistry 6 Carbohydrate Research 3 ARKIVOC 3 Monatshefte Fur Chemie 4 Indian Journal of Chemistry 2 Canadian Journal of Chemistry 4 Current Organic Synthesis 1 Bull. Korean Chemical Society Bioorg. Med. Chem. Letters J Nanosci. Nanotechnology Tetrahedron Asymmetry Nanosci. Nanotechnol. Letters Helvetica Chimica Acta RSCAdvances J. Appl. Polym. Science Chinese Journal of Chemistry Journal of Organometallic Chemistry

2 5 9 3 4 9 8 1 1 1

Current Organic Chemistry Organic Prep. &Proced. Int. Organic Biomolecular Chemistry Dig. J. Nanomater Organic Communications Catalysis Letters Natural Product Communications Green and Sustainable Chemistry Topics in Current Chemistry Topics in Heterocyclic Chemistry

1 1 10 1 1 1 1 1 1 1

21

Total 628

v 61 Papers are cited more than 50 times v 12 Papers are cited more than 100 times v 53 Papers are cited more than 53 times (h-index 53) See Annuxure-II (List of publications from 2010-15 as a Principal Author)

See Annexure-III (List of publications from 2010-15)

See Annexure-IV (Total publications from 1997-2015) 50 most cited papers of the nominee: (h-index 53: 53 Papers are cited more than 53 times)

Pub. No. Journal Year/Page Times

Cited Pub.

No. Journal Year/Page Times Cited

52 Synthesis-stuttgart 2001/783 228 100 Synthesis-stuttgart 2002/511 67 59 Synthesis-stuttgart 2001/1341 194 63 Synlett 2001/673 61 71 Synthesis- stuttgart 2001/2165 144 51 Synlett 2001/240 66

136 Tetrahedron Letters 2003/1047 143 22 Tetrahedron Letters 2000/2663 60 32 Synthesis- stuttgart 2000/1532 130 129 Green Chemistry 2002/592 73

166 J. Organic Chemistry 2003/7098 122 68 Synlett 2001/1638 70 73 Synthesis-stuttgart 2001/2277 108 246 J. Am. Chem. Soc. 2005/8974 66 77 J. C. S. Perkin Trans 1 2001/1939 105 192 Tetrahedron Letters 2004/2951 80

252 Organic Letters 2006/3391 185 153 Eur J Organic Chemistry 2003/1779 66

201 Synlett 2004/963 95 121 Chemistry Letters 2002/906 58 187 Tetrahedron 2004/1767 107 65 Tetrahedron Letters 2001/4057 60

130 Tetrahedron Letters 2002/9703 88 181 J. Mol. Cat. A: Chemical 2004/99 59

99 Tetrahedron Letters 2002/1905 90 119 Tetrahedron Letters 2002/7009 72 209 Synthesis- stuttgart 2004/2381 93 54 Synlett 2001/238 56

180 60

Eur J Organic Chemistry Synlett

2004/546 2001/1131

101 84

24 Tetrahedron Letters 2000/2695 53

43 J. Chem. Research (S) 2000/354 77 207 Tetrahedron Letters 2004/5873 63

191 Eur J. Organic Chemistry 2004/552 81 223 Tetrahedron Letters 2005/2687 64

46 Tetrahedron Letters 2001/89 66 116 Tetrahedron Letters 2002/5437 60 41 Synlett 2000/1450 69 167 Tetrahedron Letters 2003/6493 60

245 Organic Letters 2005/2699 71 194 Synthesis- stuttgart. 2004/901 60

140 Adv. Synthesis & Catalysis 2003/349 81 128 J. Chem. Soc. Perkin

Trans 1 2002/2390 59

133 Tetrahedron 2003/1599 70 270 Tetrahedron Letters 2007/2205 57

142 J. Organic 2003/2525 55

22

Chemistry 75 Tetrahedron Letters 2001/8063 70 224 Synthesis 2005/480 55

132 New Journal Chemistry 2003/462 71 138 Synthesis 2003/247 53

449 Angew. Chem. Int. Ed 2010/5961 120 184 Tetrahedron 2004/2131 53 16(e)* Complete list of publications with foreign collaborators (indicating your status as author):

S. No. Author Title Journal Year Vol. Page No.

Status of author

1.

B. V. Subba Reddy,* A.Venkateswarlu, Prashant Borkar, J. S. Yadav, B. Sridhar, René Grée

Tuning the reactivity of Oxygen/Sulfur by acidity of the catalyst in Prins cyclization: oxa- vs thiaselectivity

J. Org. Chem.

2014

79 2716

Principal author

2. B. V. Subba Reddy,* P.Borkar, J. S. Yadav, P. P. Reddy, A. C. Kunwar, B. Sridhar, René Grée

Oxidative Prins and Prins/Friedel-Crafts cyclizations for the stereoselective synthesis of dioxa bicycles & hexa hydro-1H-benzo[f]iso chromenes via C-H activation

Org. Biomol. Chem

2012 10 1349 Principal author

3. S. Chauhana, G. P. Manea, C. Ananda, D. S. Dhawalea, B. V. Subba Reddy, S. M. J. Zaidic, Salem S. Al-Deyabd, V. V. Balasubramaniana, T. Moria, A. Vinu

Low-temperature synthesis of pyrano- and furo[3,2-c]quinolines via Povarov reaction using a highly ordered 3D nanoporous catalyst

Synlett 2012 - 2237 Co-author

4. Prashant Borkar, Pierre van de Weghe, B. V. Subba Reddy, J. S. Yadav and René Grée

Unprecedented synergistic effects between weak Lewis and Brønsted acids in Prins cyclization

Chem. Commun.

2012 48 9316

Co-author

5. B. V.Subba Reddy,* Dudhmal N. Chaya, J. S.Yadav, René Grée

A concise and diastereoselective synthesis of piperidine and indolizidine alkaloids via aza-Prins reaction

Synthesis 2012 - 279 Principal author

23

6. B. V. Subba Reddy,*

Prashant Borkar, J. S. Yadav, B. Sridhar, René Grée

Tandem Prins/ Friedel-Crafts cyclization for the stereoselective synthesis of tricycles

J. Org. Chem. 2011 76 7677 Principal author

7. B.V.Subba Reddy,* K. Ramesh, A.V. Ganesh, G.G.K.S. N. Kumar, J.S. Yadav, René Grée

Triflic acid-promoted aza-Prins-Ritter reaction sequence: a novel synthesis of 4-amidopiperidines

Tetrahedron Letters


8. B.V. Subba Reddy,*

Prashant Borkar, P. Pawan Chakravarthy, J. S. Yadav, Rene Gree

Sc(OTf)3-catalyzed intramolecular aza-Prins cyclisation for the synthesis of heterobicycles

Tetrahedron Letters

2010 51 3412

Principal author

9. J.S.Yadav,* P. Borkar, P. P. Chakravarthy, B. V. Subba Reddy, A. V. S. Sarma, B. Sridhar, René

Intramolecular aza-Prins and Prins cyclization of aryl epoxides: a novel synthesis of diaza-, oxa-aza- and dioxa-bicycles

J. Org.Chem. 2010 75 2081 Co- author

10. J. S. Yadav,* B. V. Subba Reddy, K. Ramesh, G. G. K. S. N. Kumar, René Grée

An expeditious synthesis of 4-fluoropiperidines via aza-Prins cyclization

Tetrahedron Letters

2010 51 1578 Co- author

111. J. S. Yadav,* B. V. Subba Reddy, K. Ramesh, G.G.K.S.N. Kumar, René Grée

A novel aza-Prins-Friedel–Crafts reaction for the synthesis of 4-arylpiperidines

Tetrahedron Letters

2010 51 818 Co- author

12.

B.V. Subba Reddy,*A. Venkateswarlu, Ch.Madan, Ajayan Vinu

Cellulose-SO3H: an efficient, biodegradable solid acid for the synthesis of quinazolin-4(1H)-ones

Tetrahedron Letters


13.

K. K. R. Datta, B. V. Subba Reddy, K.Ariga, Ajayan Vinu*

Gold nanoparticles embedded in a mesoporous Carbon nitride stabilizer for highly efficient 3CC reaction

Angew. Chem. Int. Engl. Ed.,

2010 49 5961 Co author

24

14.

M. A. Chari, D. Shobha, El-Refaie Kenawy, S. S. Al-Deyab, B.V.Subba Reddy, Ajayan Vinu*

Nanoporous alumino silicate catalyst with 3D cage-type porous structure catalyst for benzimidazoles

Tetrahedron Letters

2010 51 5195 Co author

15.

S. Chauhan, R. Chakravarti, S. M. J. Zaidi, S. S. Al-Deyab, B.V. Subba Reddy,* Ajayan Vinu *

Efficient synthesis of 2,3,4-trisubstituted quinolines via Friedländer annulation with nanoporous cage- aluminosilicate AlKIT-5

Synlett 2010 - 2597 Principal author

16.

B.V.Subba Reddy,*A. Venkateswarlu, G.G.K.S. N.Kumar, Ajayan Vinu

Cellulose-SO3H as a recyclable catalyst for the synthesis of tetrahydropyranols via Prins cyclization

Tetrahedron Letters


17.

T. S. Naidu, V. V. B. Subramanian, M. A. Chari, T. Mori, S. M. J. Zaidi, S. S. Al-Deyab, B. V. Subba Reddy,* Ajayan Vinu*

Highly efficient Friedel-Crafts alkylation of indoles and pyrrole catalyzed by mesoporous 3D aluminosilicate catalyst with electron-deficient olefins

Synlett 2010 - 2813 Principal author

18.

Ajayan Vinu,* P. Kalita, H. Oveisi, M.A.Chari, R.Pal, B.V. Subba Reddy*

Novel synthesis of tetrahydro-β-carbolines, tetrahydroisoquinolines via three-component reaction using hexagonally ordered mesoporous AlSBA-15

Tetrahedron Letters


19.

Ajayan Vinu,* P.Kalita, V. V. B, Subramanian, H.

Mesoporous aluminosilicate nanocage catalyzed

Tetrahedron Letters


25

Oveisi, T. Selvan, A. Mano, B.V. Subba Reddy*

three-component coupling reaction: synthesis of µ-amino phosphonates

20.

B. V. Subba Reddy, L. R. Reddy, E. J. Corey*

Novel acetoxylation and C-C coupling reactions at unactivated positions in a-amino acids

Organic Letters

2006 8 3391 Co author

21.

L. R. Reddy, B. V. Subba Reddy, E. J. Corey*

Efficient method for selective introduction of substituents as C-(5) of Isoleucine and other a-amino acids

Organic Letters

2006 8 2819 Co author

22.

L. R. Reddy, J. F. Fouernier, B. V. Subba Reddy, E .J. Corey*

New synthetic route for the enantioselective total synthesis of salinosporamide A and its biologically active analogues

Organic Letters

2005 7 2699 Co author

23.

L. R. Reddy, J. F. Fouernier, B. V. Subba Reddy, E .J. Corey*

An efficient, stereo-controlled synthesis of a potent omuralide-salinosporin hybrid for selective proteasome inhibition

J. Am. Chem. Soc.

2005 127 8974 Co author

24.

L. R. Reddy, P.Sarvan an, J. F. Fouernier, B. V. Subba Reddy, E. J. Corey*

Enantiospecific syntheses of the C(2)-diastereomers of omuralide and 3-methylomuralide

Organic Letters

2005 7 2703 Co author

25.

B. V. Subba Reddy, L. R. Reddy, E .J. Corey*

Dimethylaluminium methyltellurate, a new reagent for the cleavage of hindered methyl esters

Tetrahedron Letters

2005 46 4589 Co author

16(f)* List of papers published in Conferences /Symposia/ Seminars, etc: Several research papers were presented in various conferences as invited, plenary or oral presentations by the nominee and poster and oral presentations by group members.

26

16(g) List of the most outstanding Technical Reports/ Review Articles:

S. No Author Title Journal Year Vol Page

nos. 1. B V Subba

Reddy “Multicomponent Reactions using Indium(III) salts”

Current Organic Chemistry,

2010 14 414-424

2. B V Subba Reddy

“Recent Developments on Indium Metal and its Salts in Organic Synthesis”

Eur. J. Organic Chemistry

2010 - 591-605

3. B V Subba Reddy

Recent Advances in the Applications of Ionic Liquids for the Synthesis of Bioactive Six-Membered N-Heterocycles

Current Organic Synthesis

2011 - 787-809

4. B V Subba Reddy

Recent progress in Transition Metal Catalysed Hydrofunctionalisation of Less Activated Olefins

Journal of Organometallic Chemistry

2011 696 16-36

17. Statement regarding collaboration with scientists abroad

In the last few years our group has initiated research collaborations with the following groups in abroad:

v Prof. Rene Gree, Université de Rennes 1, France.

v Prof Van de Waghe, Université de Rennes 1, France.

v Prof.Oliver Reiser, University of Regensburg

v Dr Ravisubramanyam, Colgate-Palmolive Company, USA.

v Prof. Ajan Vinu, Australian Institute for Bioengineering and Nanotechnology The University of Queensland, Australia (Previous affiliation: "National Institute for Materials Science, 1-1, Namiki, Tsukuba, Ibaraki 305-0044, Japan).

Description about International Collaborations:

Dr Reddy has a long term collaboration with Prof. Rene Gree as a part of Indo-French Joint Laboratory (CNRS-URI/CSIR) and published 10 research papers under this collaboration. Dr Reddy was involved in the synthesis of piperdine scaffolds such as 2,4-diarylpiperidines, 2-aryl-4-fluoropiperidines, 2-aryl-4-hydroxypiperidines and 4-amido-2-arylpiperidines for the evaluation of CNS activity. Subsequently, he worked on intramolecular version of Prins, aza-Prins and thia-Prins cyclization to gererate diaxa-, diaza-, oxa-thia- and dithia-heterobicycles. Under this collaboration, two of his students worked on joint projects with Prof Rene Gree at Université de Rennes 1.

27

Max Planck Institute of Molecular Physiology, Dortmund, Germany

Dr Reddy has been established a collaboration with Prof. Herbert Waldman at Max Planck Institute of Molecular Physiology, Dortmund, Germany as a AvH fellow to generate natural products inspired chemical libraries. The nominee was actively involved in the synthesis of seven-membered benzoxepine and eight-membered benzoxocine scaffolds employing Au(I)-catalyzed ene-yne cyclizations. These benzoxepine and benzoxocine moieties are core structures of Heliannuols (allelochemicals) which are isolated from sun flower oil. Some of these molecules are found to exhibit cytotoxicity against leukemia cancer cell lines. The nominee initially developed novel synthetic route to construct medium size rings via Au(I)-catalyzed ene-yne cyclization. Presently, the nominee is working on olefin functionalization of benzoxocine to generate a large number of Heliannuol analogues for biological evaluation.

Univesity of Regensburg (INDIGO program)

Dr Reddy has initiated another research collaboration with Prof.Oliver Reiser, Department of Organic Chemistry, University of Regensburg, Germany to work on catalytic C-O bond activation using Visible Light or Blue LEDs/green LEDs. Under INDIGO program, one of the PhD students (Viktor Kias) of Prof Reiser worked with Dr Reddy for three months. Both groups are presently involved in Photoredox catalysis using Ru(bpy)3Cl2/hυ.

National Institute for Materials Science (NIMS), Tsukuba, Japan

Dr Reddy has been a long term collaboration with Prof. Ajayan Vinu as a part of IICT-NIMS Joint Laboratory and published 9 research papers under Indo-Japan Collaboration. Under this joint collaboration, Dr Reddy has explored the catalytic application of Mesoporous/Nanoporous aluminosilicates such as Al-KIT5 (mesoporous 3D aluminosilicate nanocage catalyst with large cage type pores), AlSBA-15 (well-ordered mesoporous hexagonal structure), Copper substituted KIT-5 (Cu-KIT5), Iron substituted KIT-5 (Fe-KIT5) for various transformations like one-pot synthesis of tetrahydro-β-carbolines and tetrahydroisoquinolines; three-component reaction for the preparation of α-aminophosphonates; synthesis of benzimidazole derivatives and three component synthesis of propargyl amines (A3 Coupling reaction) using gold nanoparticles embedded in mesoporous carbon nitride. In addition to this, biodegradable solid acids like Cellulose-SO3H/Chitosan-SO3H have been used to perform Prins cyclization, quinazoline synthesis and quinoline synthesis.

Colgate-Palmolive Company

In collaboration with Colgate-Palmolive Company, Dr Reddy has developed a novel process for Fluorescein Dyes (MPA and NPA) and Anthocyanin Dyes (Benzopyrylium Salts) for application in Hand-Wash (Liquid Aquarium Soap). Subsequently, he has developed a breakthrough technology for making natural products such as honokiol and magnolol and their derivatives, which are known to exhibit potent anti-bacterial activity. Of these, 3,3'-dialkyl-2,2'-dihydroxybiphenyls are found to be more active than a well known anti-bacterial agent, triclosan in tooth paste. These molecules are under clinical trials to replace trichlosan from the tooth paste.

28

Meanwhile, he has also developed a novel synthetic route for ester quats (from epichlorohydrin) to use in dish wash, shaving cream and shapoo as surfactants. Presently, he is involved in the process development of hinokitiol which also shows a promissing anti-microbial activity. Recently, he has initiated a research on the synthesis of poly(allyl)guanidine hydrochloride for Gum Tissue Graft Surgery.

18. (a) List of Patents taken, if any: Two

(i) Processes for making magnolol derivatives (US patent 8,519,197 B2)

(ii) Process for producing propyl isopropylmagnolol (PCT/IN2013/000049) were filed in collaboration with Colgate-Palmolive Company. These technologies were successful transferred to Colgate-Palmolive Company.

(b) Total number of patents: Two

19. Details of Books published, if any:

(i) Sulfamic Acid in book entitled “Electronic Encyclopedia of Reagents for Organic Synthesis”

published in 2007.

(ii) Indium Catalyzed Synthesis of Heterocycles via Cycloadditions, Chap 10, Vol 13, pp 99-

171, in book entitled “Topics in Heterocyclic Chemistry” 2008, Springer Berlin/Heidelberg.

(iii) Organic Synthesis using Bismuth in book entitled “Topics in Current Chemistry” 2012,

311, 229.

20. Any additional information of relevance:

Recognized as a PhD guide in Chemistry from various Universities such as University of Hyderabad, Osmania University, Kakatiya University, Sri Venkateswara University, Yogi Vemana University, Adikavi Nannaya University, JNTU-Hyderabad, AcSIR-New Delhi) and also in Pharmaceutical Sciences (College of Technology, Osmania University). He has guided six M.Pharmacy students from NIPER, Hyderabad; two M.Pharmacy students from Department of Pharmacy, Sri Krishna Devaraya University; five M.Pharmacy students from Department of Pharmacy, College of Technology, Osmania University and two M.Pharmacy students from Department of Pharmacy, Kakatiya University. He has also guided four M.Sc students from Osmania University College for Women, Hyderabad) and four M.Sc students from JNTU Anantapur. He maintains a highly unique distinction of leading a team of Ph.D. students from Chemistry, and Pharmacy. Therefore, the work force is drawn from different disciplines and mostly working on two focused areas: (i) asymmetric synthesis (ii) novel synthetic methodologies for the generation of library of NCEs for drug discovery program. Dr. Reddy has successfully led the research group of 20-30 research scholars. Dr. Reddy has taken a strong lead to organize seminars like Organic Synthesis for Human Wellbeing: Emerging Opportunities and Challenges; Chemistry and Chemical Biology of Natural Products and workshops such as Indo-Japan; Indo-French and Indo-German workshops held at IICT.

Annexure I (Citations from 2008 onwards)

12d (i) Citations of the papers published from 2008 onwards (without self citations). Only those Papers which are cited more than 15 times are given Pub. No. Author Year Journal Vol. Page 542 Reddy, BVS (Cited

19 times) 2013 Organic Letters 15 464

Bhardwaj V Feng J Jeon H Zhang Y Dinda B Gujarathi S Cui H Li Y Li B Dawande S Kim C Goriya Y Yang W Liu G Liu J Kandhasamy S Ishida Y Miura T Gao W

2015 2014 2014 2014 2014 2014 2014 2014 2014 2014 2014 2014 2014 2014 2013 2013 2013 2013 2013

RSC advances Tetrahedron Letters Journal of organic chemistry Organic Letters European Journal of Organic Chemistry Tetrahedron Organic & Biomolecular Chemistry Journal of organic chemistry New Journal of Chemistry Angew Chem International Edition Organic Letters Chemical Communications RSC advances Organic & Biomolecular Chemistry Journal of Chemical and Engineering Data Journal of Chemical Sciences Heterocycles Organic Letters Chemical Communications

5 55 79 16 -

70 12 79 38 53 16 50 4 12 58

125 87 15 49

15233 6455 9865 4558 5521

5267 5822 5929 2435 4076 1900 7790 15007 1387 3309

967

1691 3298 4890

487 Reddy, BVS (Cited

15 times) Tayade Y Havrylyuk D Brahmachari G Swetha A Gangarapu K Han K Maddela S Yu J Mei L Armstrong E Pingaew R Kiran G Ren Y M Biersack B Gangarapu K

2012 2015 2015 2014 2014 2014 2014 2014 2014 2014 2013 2013 2013 2013 2012 2012

Bioorganic & Medicinal Chemistry Letters Tetrahedron Letters Mini-Reviews in Organic Chemistry ACS Substainable Chemistry & Engineering Tetrahedron Letters Medicinial Chemistry Research Bioorganic & Medicinal Chemistry Letters Toxicological and Environmental Chemsitry Synthetic communications Organic & Biomolecular Chemistry Journal of organic chemistry Molecular Diversity Toxicological and Environmental Chemsitry RSC advances Current Drug Targets Letters in Drugs

22

56 12 2

55 23 24

96

44 12 70 17 95

3 13 9

2460

666 66

2802

4705 1046 591

1

2029 1149 10534 595 367

7182 1705 934


482 Reddy, BVS (Cited 18 times)

2011 Tetrahedron Letters 52 5789

Shamim S 2014 Tetrahedron Letters 55 1159 Guillaumet G 2013 Chemistry-A European Journal 19 12249 Gryko DT 2013 Chemistry-An Asian Journal 8 1279 Hajra A 2013 Advanced Synthesis & Catalysis 355 1065 Vishwakarma RA 2013 RSC advances 3 20869 Shivashankar K 2013 RSC advances 3 20883 Samadi A 2013 European Journal of Organic

Chemistry - 35

Romanenko GV 2013 European Journal of Organic Chemistry

- 368

Loh TP 2013 Chemical reviews 113 271 Pradipta Das 2012 Tetrahedron letters 53 6418 Ping J 2012 Molecules 17 13368

Singh, KN 2012 Synlett 18 2635

Namboothiri INN 2012 Organic Letters 14 4580

Sizhuo 2012 Chemistry-An asian journal 9 2028

Rajesh M 2012 European journal of organic chemistry

26 5038

Michal K 2012 Journal of organic chemistry 77 5552

Priyadarshani G 2012 Journal of organic chemistry 77 4438

Daniela V 2012 Arkivoc - 282



Wang J 2014 Synthetic communications 44 361 Sarkar D 2014 RSC advances 4 7666 Eavani S 2014 Inorganica chimica acta 409 302 Ghahremanzadeh 2013 Acs combinatorial science 15 530 Qin Y 2013 Synthesis-stuttgart 45 2545 Moores A 2013 Synlett 24 1637 Ropali 2013 European Journal of Organic

Chemistry 24 5509

Xiao L 2013 Journal of molecular catalysis a-chemical

374 85

Hu Z 2013 Science of advanced materials 5 822 Majid M 2013 Phosphorus Sulfur and Silicon and the

related elements 188 850

Abedini M. 2013 Journal of nanoscience and nanotechnology

13 4838

Mahdi M 2013 Tetrahedron 69 4708


Reuben H 2013 Synlett 24 1309 Shi L 2013 Progress in chemistry 25 233 Youquan 2013 Chemistry-A european journal 19 3665 Saba A 2013 Heteroatom chemistry 24 174 Afshari M 2012 Sientia iranica 19 1991 Chengjian 2012 Catalysis communications 28 134 Singh B 2012 Tetrahedron 53 5497 Carlos C 2012 Tetrahedron 53 6369 Jang DO 2012 Tetrahedron Letters 53 3897 Carlos C 2012 Journal of the mexican chemical

society 56 183

Zhang T 2012 nanoscale 4 6244

kap duk 2012 phosphorus sulfur and silicon and the related elements

187 899

Sushobhan C 2012 Rsc advances 2 4547

Matveeva, E. V 2012 Russian chemical reviews 81 221

Kuk Ro 2012 Heteroatom chemistry 23 160

Yeon Tae 2011 Tetrahedron letters 52 4764 450 Reddy, BVS (Cited

35 times) 2010 European Journal Of Organic

Chemistry - 591

Belen'kii LI 2014 Advances in Heterocyclic Chemistry 111 147 Shao H 2013 Organic Letters 15 5170 Hajra A 2013 Tetrahedron Letters 54 4982 Babu A S 2013 Tetrahedron 69 6598 Michelet V 2013 Chemcatchem 8 2395 Rene G 2013 Synlett 24 1142 Lockhart M T 2013 Ultrasonics Sonochemistry 20 826 Monge M A 2013 CrystEngComm 15 9562 Babu 2013 European Journal of Organic

Chemistry - 2362

Loh TP 2013 Chemical Reviews 113 271 Maya SS 2012 Tetrahedron 68 8683 Thomas P 2012 Journal of Organic Chemistry 77 9277 Zhi XY 2012 Journal of Organic Chemistry 77 8527 Nayyar AA 2012 Eur Journal of Organic Chemistry 2012 4395 Pulak J. Bhuyan 2012 Tetrahedron Letters 53 4015 Ramana CV 2012 Chemistry-A European Journal 18 9601 Xiaoming Feng 2012 Advanced Synthesis & Catalysis 354 1508 Yuanzhi Xia 2012 Chemistry-A European Journal 18 5401 Maya Shankar 2012 Chemistry-An Asian Journal 7 778 Ndoye, Alpha 2012 Organic Letters 14 1536 Madabhushi S 2012 Tetrahedron Letters 53 697 Samai S 2012 Tetrahedron 68 1247


Tato R, 2012 Tetrahedron 68 1606 Gutierrez EG 2011 Organic Letters 13 5754 Rahman M 2011 Tetrahedron Letters 52 4437 Sakai N 2011 Tetrahedron Letters 52 3133 Hirashita T 2011 Chemistry Letters 40 506 Sakai N 2011 Eur Journal of Organic Chemistry 201 3178 Verma GK 2011 Tetrahedron 67 3698 Tsuji H 2011 Synlett - 1015 Kiyokawa K 2011 Organometallics 30 2039 Lo Fiego MJ 2011 Journal of Organic Chemistry 76 1707 Verma RK 2011 Tetrahedron 67 584 Kundu D 2011 Chemistry-An Asian Journal 6 406 Nowrouzi F 2010 Organic Letters 12 5490 431 Reddy, BVS (Cited

31 times) 2010 Tetrahedron Letters 51 3334

Wang J 2014 Angew Chem International Edition 53 2186 Wang Y 2014 Tetrahedron Letters 55 1271 Cheng J 2014 Chemical Communications 50 2315 Weiping Su 2013 Organic Letters 15 5278 Fan C 2013 Tetrahedron Letters 54 5250 Wang Y 2013 Tetrahedron 69 4236 Kwong F Y 2013 Journal of Organic Chemistry 78 3374 Cheng J 2013 Chinese journal of chemistry 31 27 Mark JK 2013 Organic Letters 15 362 Jin HL 2012 Synlett - 2491 Qiang Z 2012 Organic Letters 14 4966 Fan Chen 2012 Synlett - 2247 Chang S 2012 Organic Letters 14 3924 Alireza K 2012 Chinese Chemical Letters 23 903 Chaodong H 2012 Chemistry Letters 41 719 Ebrahim K 2012 Tetrahedron Letters 53 1900 Karen A 2012 Tetrahedron Letters 53 200 Jiao N 2012 Angew Chem International Edition 51 9226 Lei W 2012 Organic & Biomolecular Chemistry 10 7184 Jiang C 2012 Chemical Communications 48 449 Fan C 2011 Synlett - 2991 Wang, J 2011 Organic Letters 13 5608 Jiang C 2011 Organic Letters 13 5004 Jiao N 2011 J.Am. Chem. Soc 133 12374 Seth WG 2011 Tetrahedron Letters 52 3376 Hideo T 2011 Tetrahedron Letters 52 2404 Jiang C 2011 Advanced Synthesis & Catalysis 353 291 Jiang C 2011 Chemical Communications 47 6725 Miguel AR 2010 Tetrahedron 66 8828


449 Reddy, BVS (Cited

86 times) 2010 Angewandte Chemie International

Edition 49 5961

Yan F 2014 Biosensors & Bioelectronics 52 153 Chen JS 2013 Angew Chem International Edition 52 11822 Juan C. Scaiano 2013 Chem. Commun 49 1732 Datta DK 2013 Journal of Molecular Catalysis A 366 206 Zhao P 2012 Applied Surface Science 263 471 Kazushi Miki 2012 Advanced Materials 24 6462 Xu X 2012 Catalysis Communications 28 9 Subramaniann V 2012 Journal of Nanoscience and

Nanotechnology 12 8467

Mothika V 2012 ChemPlusChem 77 743 Garcia H 2012 Chemical Reviews 112 4469 Fristrup P 2012 ChemCatChem 4 1037 Tharamani C 2012 Applied Catalysis A-General 431 88 Izawa H 2012 Current Medicinal Chemistry 19 2388 Shi F 2012 Chemical Reviews 112 2467 Michael J 2012 Chemistry of Materials 24 728 Paul A 2012 Advanced Materials 24 485 Jae Y 2012 Langmuir 28 991 Khorasani M 2012 Chemical Communications 48 8961 Jonathan P 2012 Chemical Society Reviews 41 5800 Chang G 2012 Gold Bulletin 45 61 Yuan Q 2012 Journal of Materials Chemistry 22 13571 Antonietti M 2012 Chemical Science 3 2170 Ji Q 2012 Journal of Materials Chemistry 22 10389 Wang L 2012 RSC Advances 2 4632 Gurudas P 2012 Journal of Materials Chemistry 22 9831 Mano A 2012 ChemSusChem 5 700 Lu Wenbo 2012 Catalysis Science & Technology 2 711 Augustynek K 2012 Chemical Communications 48 3972 Ariga K 2012 Bulletin of Chem Soc of Japan 85 1-32 Ariga K 2012 Journal of Materials Chemistry 22 2369 Antonietti M 2012 Angew Chem. International Ed. 51 68 Climent MJ 2012 Rsc Advances 2 16 Liu S, 2012 Rsc Advances 2 411 Wu ZX 2012 Advanced Materials 24 485 Park SK 2012 Chemical Communications 48 1108 Saravanan L 2011 J. Nanoscience and Nanotechnology 11 7783 Liu S 2011 RSC Advances 1 951 Choma J 2011 Ochrona Srodowiska 33 3-8 Layek K 2011 Green Chemistry 13 2878 Sreelakshmi C 2011 J. Nanoscience and Nanotechnology 11 6995


Liu J 2011 Chemical Communications 47 11119 Ariga K 2011 Chemical Record 11 199 Zhao JW 2011 Journal of Materials Chemistry 21 13926 Zhu FX 2011 Journal of American Chemical Society

133 11632

Ariga K 2011 Advanced Drug Delivery Reviews 63 762 Liu S 2011 Journal of Materials Chemistry 21 11726 Wei YC 2011 Energy & Environmental Science 4 2959 Datta KKR 2007 Journal of Nanoscience and


Corma A 2011 Chemical Reviews 111 1657 Datta KKR 2011 Journal of Nanoscience and


Datta KKR 2011 Chemistry-A European Journal 17 3390 Wei YC 2011 Angewandte Chemie International 50 2326 Haque E 2010 Journal of Materials Chemistry 20 10801



Sarkar D 2013 RSC Advances 4 7666 Heydari A 2013 Tetrahedron Letters 54 6403 Qin Y 2013 Synthesis - stuttgart 45 2545 Abedini M 2013 Journal of nanoscience and

nanotechnology 13 4838

Sadeghzadeh.Mm 2013 Journal of chemical sciences 215 537 Ajayan V 2013 Chemcatchem 5 899 Ajayan V 2013 Synlett 15 2237 Ajayan V 2013 Microporous and mesoporous 167 146 Ajayan V 2012 Tetrahedron Letters 53 5656 Baldev S 2012 Tetrahedron Letters 53 5497 Ajayan V 2012 Tetrahedron Letters 53 1485 Ajayan V 2012 Angew Chem International Ed. 51 2859 Sara I 2012 RSC Advances 2012 16 Ajayan V 2011 Synlett 2011 1923 Chris VS 2011 Current Organic Chemistry 15 2015 Jun Tang 2011 Jornal of Fluorine Chemistry 132 102 Banerji J 2011 Arkivoc - 161 Zhan H 2011 Applied Organometallic Chemistry 25 47 Ajayan V 2010 Tetrahedron Letters 51 5195 Sun GY 2010 Journal of Chinese Chemical Society 57 1315 Ajayan V 2010 Tetrahedron Letters 51 2629 Amir N 2010 Heteoaton Chemistry

21 418



2008 Journal of Organic Chemistry 73 6857

Fakhari A 2014 Tetrahedron Letters 55 333 Guo C 2013 Beilstein journal of organic chemistry 9 2934 Fabien G 2013 Organic letters 15 4234 Yan CG Beilstein journal of organic chemistry 9 846 Liu ZM 2012 Chemical Research in Chinese

Universities 28 990

Han Y 2012 Tetrahedron 68 8539 Sun Y 2012 Tetrahedron Letters 53 3647 Schmidbaur H 2012 Arabian Journal for Science and

Engineering 37 1187

Tu, XC 2012 Tetrahedron Letters 53 3169 Sun J 2012 Eur. J. Org. Chemistry - 1976 Wu L 2012 Chinese Journal of Chemistry 30 590 Sun Y 2012 Molecular Diversity 16 163 Wu L 2012 Organic &Biomolecular Chemistry 10 9452 Xin Y 2012 Journal of Fluorine Chemistry 133 97 Yamuna E 2011 Tetrahedron Letters 52 6805 Sun J 2011 Eur. J. Org. Chem - 6952 Sun J 2011 ACS Combinatorial Science 13 421 Corma A 2011 Chemical reviews 111 1657 Shen H 2010 Journal of American Chemical Society 132 11473 Sun J 2010 Organic Letters 12 3678 Enomoto T 2009 Journal of Organic Chemistry 74 9158 Kothandaraman P 2009 Journal of Organic Chemistry 74 5947 Kumaraswamy G 2009 European Journal of Organic

Chemistry - 4158

Okamoto N 2009 Tetrahedron Letters 50 4167 Petasis NA 2009 Journal of Organometallic Chemistry 694 1747 350 Reddy, BVS (Cited


Silva Jr LF 2013 Synthesis - stuttgart 45 1076 Timothy P 2013 RSC Advances 3 25498 Hasegawa E 2012 Heterocycles 86 1211 Yus M 2012 Current Organic Chemistry 16 1277 Dake S 2012 Current Organic Chemistry 16 1485 Miura K 2012 Heterocycles 86 1211 Parchinsky V 2011 Tetrahedron Letters 52 7157 Srinivasan P 2011 Ind. J. Chem. Sec. B-Org.Chem.

Including Med Chem. 50 1083

Chio FK 2011 Tetrahedron 67 5107 Veisi H 2011 Current Organic Chemistry 15 2438 Majumdar KC 2010 Current Organic Chemistry 15 1760 Hasegawa E 2010 Tetrahedron Letters 51 6535


Sabitha G 2010 Helvetica Chimica Acta 93 9533 Launay GG 2010 Beilstein Journal of Organic

Chemistry 6 41

Kinoshita H 2010 Journal of American Chemical Society

132 6412

Carballo RM 2010 European Journal of Organic Chemistry

- 2304

Jin HJ 2010 Chemical Journal of Chinese Universities-Chinese

31 514

Dobbs AP 2010 Organic & Biomolecular Chemistry 8 1064 Olier C 2010 Tetrahedron 66 413 Silva LF 2009 Tetrahedron Letters 50 2256 351 Reddy, BVS (Cited


Roy S 2013 Tetrahedron 69 942 Rahmati A 2012 Catalysis Communications 29 122 Roy S 2012 Tetrahedron 68 3776 Rafiee E 2011 Canadian Journal of Chemistry-Revue

Canadienne De Chimie 89 1533

Aridoss G 2011 Tetrahedron Letters 52 6859 Chatterjee PN 2011 Tetrahedron 67 4569 Aridoss G 2011 Organic & Biomolecular Chemistry 9 2518 Emer E 2011 European Journal of Organic

Chemistry - 647

Maiti S 2011 Synthetic Communications 41 243 Sanz R 2010 European Journal of Organic

Chemistry - 7027

Reddy CR 2010 Synthesis-Stuttgart - 3715 Theerthagiri P 2010 Tetrahedron Letters 51 5454 Wang JC 2010 Synlett - 2493 Liu PN 2010 Journal of Organic Chemistry 75 5017 Correia CA 2010 Tetrahedron Letters 51 1172 Rueping M 2010 Beilstein Journal Of Organic

Chemistry 6 6

Wang HJ 2009 Journal of Brazilian Chemical Society

20 1939

Damu GLV 2009 Tetrahedron Letters 50 6154 Shushizadeh MR 2009 Chinese Chemical Letters 20 1068 Funabiki K 2009 Tetrahedron 65 7457 Damm M 2009 Journal of Combinatorial Chemistry 11 460 Kumar PS 2008 European Journal of Organic

Chemistry

- 6063



2008 SYNTHESIS 395

Heravi MM 2013 Green chemistry letters and reviews

6 282

Xiao C 2013 Journal of medicinal chemistry 56 8019 Min 2013 Synlett 24 2292 Talipova GR 2013 Reaction kinetics mechanisms and

catalysis 110 41

Luiz Jr F 2013 Journal of the brazilian chemical society

24 1414

Nabajyoti H 2013 Synlett 24 1137 Talipov R. F 2013 Computational and theoretical

chemistry 1013 57

Tamura Y 2013 Bioorganic & medicinal chemistry letters

22 6554

Feng X 2012 Journal of American Chemical Society 134 17564 Miguel Y 2012 Current organic chemistry 16 1277 Sujata V 2012 Green chemistry letters and

reviews 5 13

Borah Ruli 2012 Journal of chemical sciences 123 623 Bertrand MP 2010 Tetrahedron 66 413 Kuroda C 2009 Helvetica chimica acta 92 1333 Zhang ZH 2009 Journal of the brazilian chemical

society 20 1939

Scott RD 2008 Organic Letters 10 4839 Scott RD 2008 Journal of American Chemical Society 130 13177 Hiyoshizo K 2008 Heterocycles 76 73 348 Reddy, BVS (Cited

20 times) 2008 TETRAHEDRON LETTERS 49 2815

Lin J 2014 Tetrahedron 70 1047

Fakhari AR 2014 Tetrahedron Letters 55 333 Wang L 2013 Advanced synthesis & catalysis 355 765 Nassiri M 2013 Synthetic communications 43 157 Shiri Morteza 2012 Chemical Reviews 112 3508 Riyadh S M 2011 Molecules 16 8244 Hosseinabadi R 2011 Tetrahedron Letters 52 4865 Nassiri M 2011 Journal of Chemical Research - 437 Zhang J 2011 Tetrahedron 67 2060 Behbehani H 2011 European Journal of Medicinal

Chemistry 46 1813

Karimi Z 2011 Journal of Chemical Research - 1-3 Nassiri M 2010 Journal of Chemical Research - 365 Nassiri M 2010 Arkivoc - 61


Moghaddam FM 2010 Tetrahedron 66 3678 Xia EY 2010 Tetrahedron 66 3569 Fodor L 2010 Monatshefte Fur Chemie 141 431 Anary AM 2010 J. Brazilian Chemical Society 21 319 Yu XX 2010 Journal of Combinatorial Chemistry 12 238 Moghaddam FM 2010 Synlett - 123 Moghaddam FM 2010 Tetrahedron 66 134 369 Reddy, BVS (Cited


Yoshida J 2013 Journal of American Chemical Society 135 16070 Wu AX 2013 Tetrahedron 69 7038 Nachtsheim BJ 2013 Journal of organic chemistry 78 6065 Nachtsheim BJ 2013 Synthesis-stuttgart 45 979 Deveaux K 2012 Heterocyclic Communications 18 181 Mei cai 2012 Organic Letters 14 4414 Techajaroonjit T 2012 Synthesis 44 1693 Donohoe TJ 2012 Organic & Biomolecular Chemistry 10 1093 Boulange A 2011 Chemistry-A European Journal 17 10241 Liu JH 2011 Tetrahedron Letters 52 4320 Salama TA 2011 Tetrahedron Letters 52 4026 Zhdankin VV 2011 Journal of Organic Chemistry 76 1185 Duschek A 2011 Angew Chemie-International Ed. 50 1524 Deshmukh SS 2011 Synlett - 81-83 Donohoe TJ 2010 Synlett - 2956 Tan JN 2010 Green Chemistry 12 1772 Satam V 2010 Tetrahedron 66 7659 Nobuta T 2010 Synlett - 2325 Nobuta T 2010 Synlett - 2335 Gao M 2010 Organic Letters 12 1856 Moorthy JN 2009 Journal of Organic Chemistry 74 6287 Moorthy JN 2009 Tetrahedron Letters 50 2493 322 Reddy, BVS (Cited

19 times) 2008 TETRAHEDRON LETTERS 49 2031

González JM 2013 Advanced synthesis & catalysis 355 3337 Álvarez M 2013 Chemical reviews 113 4567 Zhong Z 2012 Journal of Organometallic Chemistry 721 164 Dake SA 2012 Current Organic Chemistry 16 1485 Liu Xiaoqing 2012 Journal of Fluorine Chemistry 133 127 Yang F 2011 Tetrahedron 67 10147 Campos CA 2011 Organic Letters 13 5680 Srinivasan P 2011 Ind. J. Chem. Sec. B-Org.Chem.

Including Med Chem. 50 1083

Wang T 2011 Organic Letters 13 3324 Yang F 2011 Chemical Communications 47 4541


Yang F 2011 Chemical Communications 47 4013 Lin M 2011 Chemistry Letters 40 111 Yang F 2011 Tetrahedron Letters 52 936 Jereb M 2010 Tetrahedron 67 1355 Wang T 2010 Green Chemistry 12 1576 Jereb M 2009 Acta Chimica Slovenica 56 652 Jereb M 2009 Tetrahedron Letters 50 2347 Yadav JS 2009 Organic Letters 11 1705 365 Reddy, BVS (Cited

33 times) 2008 SYNTHESIS-STUTTGART - 3787

Xiao Y 2014 Dyes and pigments 102 1-5 Khanjari H 2014 Transition metal chemistry 39 47-54 Robinson RS 2014 Tetrahedron letters 55 642 Mohamadi A 2013 Polycyclic aromatic compounds 33 419 Rezanejade G 2013 comptes rendus chimie 16 872 Wei Z 2013 Journal of Organic Chemistry 78 5932 Zine R 2013 Journal of Sulfur Chemistry 34 242 Ali A 2013 Chemical reviews 113 2958 Chen B 2013 Tetrahedron Letters 54 1627 Chang J 2013 Journal of heterocyclic chemistry 50 293 Ghasem RB 2013 Microporous and Mesoporous

Materials 169 67

Santosh GT 2012 Tetrahedron Letters 54 1003 Anxin W 2012 Tetrahedron 68 9598 Ghasem RB 2012 Catalysis Communications 27 49 Song J 2012 Synlett - 2416 Hu ZY 2012 Asian Journal of Chemistry 24 2262 Schmidt B 2012 European Journal of Organic

Chemistry - 1439

Rahmatpour A 2012 Heteroatom Chemistry 23 472 Lihong H 2012 Synthetic Communications 42 236 Narsaiah A 2012 Synthetic Communications 42 883 Huang T 2011 Synthetic Communications 41 3334 Song WB 2012 Synthetic Communications 42 236 Shamsi M 2011 Arkivoc - 252 Alinezhad H 2011 Bulletin of Korean Chemical Society 32 3720 Chavan HV 2011 Journal of Chemical Sciences 123 477 Ostrowska K 2011 Tetrahedron 67 5219 Li J 2011 Journal of Heterocyclic Chemistry 48 403 Subrahmanyam CS 2011 Asian Journal of Chemistry 23 1331 Martin LJ 2011 Organic Letters 13 320 Hou JT 2010 Journal of Heterocyclic Chemistry 47 703 Venkateswarlu Y 2010 Letters In Organic Chemistry 7 208 Majumdar KC 2010 Current Organic Chemistry 14 846 Zhang XZ 2010 Chinese Chemical Letters 21 395



2008 TETRAHEDRON LETTERS 49 5683

Tetsuya T 2014 Chemistry-an asian journal 9 305 Zhiwei M 2013 Advanced Synthesis & Catalysis 355 589 Jeh-Jeng W 2012 Advanced Synthesis & Catalysis 354 2218 Lin H 2012 Synthetic Communications 42 1226 Malek T 2011 Tetrahedron 67 8492 Jinxing Y 2011 Synthesis-Stuttgart - 1984 Giovanni C 2011 Chemical Reviews 111 3076 Rosaria V 2011 Tetrahedron 67 2768 Marjan J 2011 Tetrahedron 67 1355 Lin He 2010 Synlett - 2513 Ning Z 2010 Advanced Synthesis & Catalysis 352 1291 Wei W 2010 Chemistry: An Asian Journal 5 1303 Zhou Y 2009 Chinese Journal of Organic

Chemistry 29 1719

Zeng J 2009 Canadian Journal of Chemistry 87 1209 Giovanni C 2009 Synlett - 1525 Zeng J 2009 Journal of Chemical Research - 374 12 Papers cited more than 100

times

52

Reddy, BVS (Cited 228 times)

2001

Synthesis-stuttgart

5

783


2001 Synthesis-stuttgart 9 1341


2006 Organic Letters 8 3391



136 Reddy, BVS (Cited 143times)





2003 Journal of Organic Chemistry 68 7098


2010 Angew Chem Int. Ed 49 5961



77 Reddy, BVS (Cited 105times)

2001 Perkin Transactions 1 16 1939


2004 Tetrahedron 60 1767


2004 Eur J Org Chem 3 546


12d (ii) Citations of the nominee’s publications in text books and book chapters from 2007 onwards:

S.No Author Book Year Vol. Page (1) Reddy, BVS Topics in Current Chemistry: Bismuth-

Mediated Organic Reactions 2012 311 229

288 Journal of Molecular Catalysis A: Chemical 2007 271 161 115 Synth Commun 2002 32 1803 153

46 49 181 160 403 177 258 276 44 64 306 315 357 161 213 201 208 316 179 185 155 205

Eur J Org Chem Tetrahedron Lett Synthesis J Mol Catal A: Chem Tetrahedron Lett Catal Letters Synthesis Synthesis J Mol Cat A: Chemical Synth Commun Synthesis Tetrahedron Lett Tetrahedron Lett Can J Chem Synthesis Chem Lett Synlett Tetrahedron Lett Can J Chem Synthesis Tetrahedron Lett Tetrahedron Lett Tetrahedron Lett

2003 2001 2001 2004 2003 2009 2004 2006 2007 2001 2001 2007 2007 2008 2003 2004 2004 2004 2008 2004 2004 2003 2004

- 42 - 210 44 131 - - 271 31 - 48 48 86 - 33 - 45 86 - 45 44 45

1779 89 885 99 6501 480 1854 4121 160 1075 1065 7155 8874 769 1387 1436 963 5873 124 2523 1543 4861 6037

(2) T. Lindel Topics in Current Chemistry. Indole Prenylation in Alkaloid Synthesis

2012 309 67

105 Tetrahedron Letters 2002 43 5185 (3) S. Minakata Topics in Heterocyclic Chemistry 2012 27 139 301 Tetrahedron Letters 2007 48 7034 (4) Akiya Ogawa Topics in Organometallic Chemistry 2012 - 1-36 311 Chemistry Letters 2007 36 1474 (5) Ali Mohammad Green Solvents II 2012 - - 134 Tetrahedron 2003 59 1805 (6) J. D. Hepworth Progress in Heterocyclic Chemistry, Chapter

6.4 -Six-Membered Ring Systems: With O and/or S Atoms

2011 22 449

424 Tetrahedron Letters 2010 51 2963 (7) Dennis G. Hall Boronic Acids: 2011 - - 283 Journal of Molecular Catalysis A: Chemical

2007 274 101

(8) Jonathon S. Russel Progress in Heterocyclic Chemistry Chapter 5.2 –Five-Membered Ring Systems: Pyrroles and Benzo Analogs

2011 22 143

411 Tetrahedron Letters 2010 51 244 (9) Min Shi The Chemistry of the Morita-baylis-Hillman

Reaction 2011 - 147


305 293

Tetrahedron Letters Tetrahedron Letters

2007 2007

48 48

7546 4169

(10) A. C. Knipe Electrophilic Aromatic Substitution 2011 - 23 144 229 411

Tetrahedron Letters Tetrahedron Letters Tetrahedron Letters

2003 2005 2010

44 46 51

2221 639 244

(11) R. J. Sundberg Topics in Heterocyclic Chemistry Electrophilic Substitution Reactions of Indoles

2011 26 47

105 Tetrahedron Letters 2002 43 5185 192 Tetrahedron Letters 2004 45 2951 (12)

J. Alvarez-Builla Modern Heterocyclic Chemistry Three-Membered Heterocycles. Structure and Reactivity

2011 - -

104 Tetrahedron Letters 2002 43 5105 403 Catalysis Letters 2009 131 480 (13) Min Shi The Chemistry of the Morita-baylis-Hillman

Reaction 2011 - -

293 Tetrahedron Letters 2007 48 4169 305 Tetrahedron Letters 2007 48 7546 283 Journal of Molecular Catalysis A: Chemical 2007 274 105

(14) J. S. Russel Topics in Heterocyclic Chemistry, Oxindoles and Spirocyclic Variations: Strategies for C3 Functionalization

2011 26 397

270 Tetrahedron Letters 2007 48 2029 (15) A. C. Knipe Organic Reaction Mechanisms 2011 - - 356 Tetrahedron Letters 2006 49 4742 (16) A. C. Knipe Organic Reaction Mechanisms 2011 - -

402 Tetrahedron Letters 2009 50 6642 (17) J. Alvarez-Builla Modern Heterocyclic Chemistry: 8. Five-

Membered Heterocycles: 1,2-Azoles. Part 1. Pyrazoles

2011 - -

206 Tetrahedron Letters 2004 45 3465 (18) A. C. Knipe Organic Reaction Mechanisms: Nucleophilic

Aliphatic Substitution 2010 - -

403 Catalysis Letters 2009 131 480 (19) N. Kielland Synthesis of Heterocycles via Multicomponent

Reactions II: Recent Developments in Reissert-Type Multicomponent Reactions

2010 25 127

377 Synthesis 2009 - 1131 (20) A. B. Hughes Amino Acids, Peptides and Proteins in Organic

Chemistry: Origins and Synthesis of Amino Acid, Volume 1. Synthesis of Halogenated α-Amino Acids

2010 - -

255 Chemistry Letters 2006 35 448 (21) Jason P. Tierney Microwave Assisted Organic Synthesis: Chapter

3. Heterocyclic Chemistry Using Microwave-Assisted Approaches

2009 - -

47 Synthetic Communications 2001 31 425 (22) Jason P, Tierney Heterocyclic Chemistry Using Microwave-

Assisted Approaches Chapter 3 2009 - -

99 Tetrahedron Letters 2002 43 1905 (23) Jason P. Tierney Microwave Assisted Organic Synthesis,

Chapter4. Microwave-Assisted Reductions 2009 - -

89 Synthetic Communications 2002 32 219


(24) J. Tulla-Puche The Power of Functional Resins in Organic Synthesis Chapter 5. Base and Acid Reagents

2009 -


(25) Jie Jack Li Name reactions: a collection of detailed reaction mechanisms

2009 - -

89 Synthetic Communications 2002 32 219 374 Tetrahedron Letters 2009 50 81

(26) Engelbert Ciganek Electrophilic Amination of Carbanions, Enolates, and Their Surrogates


(27) Hamid Shirani Application of Metalation reactions for synthesis of new sulfur/Selenium-Containing Heterocyclic Compounds

2009 - 1-53

301 Tetrahedron Letters 2007 48 7034 (28) H Shirani Application of Metalation reactions for synthesis

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2009 - 1 – 53

301 Tetrahedron Letters 2007 48 7034 (29) A. C. Knipe Organic Reaction Mechanisms 2009 - -

144 Tetrahedron Letters 2003 44 2221 229 Tetrahedron Letters 2005 46 639

(30) R. M. Pagni Molten salts and Ionic Liquids never the twain: Chapter 19. An Organic Chemist's Perspective on High Temperature Molten Salts and Room Temperature Ionic Liquids

2009 - -

203 Chemistry Letters 2004 33 476 (31) Levecque Introduction of (heterogeneous) catalysis in

Sugar Chemistry 2008 - -

128 J. Chem. Soc. Perkin Trans 1 2002 - 2390 (32) H. Yamamoto Acid Catalysis in Modern Organic Synthesis

Vol. 1 2008 - -

84 Tetrahedron Letters 2002 43 1565 92 Tetrahedron Letters 2002 43 2095 87 Synthetic Communications 2002 32 3519 101 Synthetic Communications 2002 32 715

(33) E. B. Rowland Enantioselective Bronsted acid-catalyzed reaction methodology. Part A: Enantioselective Mannich reaction. Part B: Enantioselective desymmetrization of meso-aziridines

2008 - -

84 Tetrahedron Letters 2002 43 1565

(34) Tamas Mallat Handbook of Heterogeneous Catalysis. Amination Reactions

2008 - -

125 Advanced Synthesis & Catalysis 2002 344 938

(35) Bernd Plietker Iron Catalysis in Organic Chemistry: Reactions and Applications, Chapter 8. Addition and Conjugate Addition Reactions to Carbonyl Compounds

2008 - -



(36) C. J. Cramer Theilheimer's Synthetic Methods of Organic Chemistry

2008 72 1-22

348 Tetrahedron Letters 2008 49 2649

(37) R. Gläser Handbook of Heterogeneous Catalysis, Heterogeneous Catalysis in Non-Conventional Solvents

2008

181 Journal of Molecular Catalysis A: Chemical 210 99-103

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2008 - 179-225

200 Tetrahedron Letters 2004 45 4583 (39) G. Andersson Modern Reduction Methods 2008 - -

205 Tetrahedron Letters 2004 45 6037 (40) A. C. Knipe Organic Reaction Mechanisms 2007 - - (41) (42)

72 Scherrmann, Marie-Christine Shiri M, Zolfigol. M. A, Kruger. H.G

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42 295 8 7 45 3 102 29 6 14

6381 1–18 773 1712 4583 546 139-227 4403 963 2381

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Advances in Heterocyclic Chemistry Synthetic Communications Synthetic Communications Green Chemistry

2006 1999 2001 2000

90 29 31 2

1-123 4403 425 115

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2011 2001 2001 2004 2004

105 16 9 33 3

223 1939 1341 926 552

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Advances in Carbohydrate Chemistry and biochemistry Tetrahedron Letters Tetrahedron Letters

2006 2001 2002

60 42 43

103 4057 7009

(46) Nubbemeyer U Natural Products Synthesis Targets Methods Synlett

2005 2000

224 4

149 487

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2006 2002

226 43

1-47 1905

(48) Taubert A Ionic liquids: Topics in current chemistry J Chemical Society Perkin Transactions 1

2009 2002

290 21

127 2390

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2011 2008

33 49

1 – 26 4742

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2010 2006 2002

99 20 43

143 3447 8133


(51) Gyorgydeak Zoltan. Tiem Joachim

Advances in carbohydrate chemistry and biochemistry Synthesis - stuttgart

2010 2006

63 17

29-99 2923

(52) El Ashry. El Sayed H. Awad Laila F.

Advances in Heterocyclic Chemistry Tetrahedron Letters Synlett

2009 2004 2004

98 17 6

1-141 3493 963

(53) Moore. L. Rovis. T Asymmetric Organocatalysis Topics in Current Chemistry Tetrahedron Letters

2009 2003

291 44

77-144 8959

(54) Sereda. O. Sobia. W Rene

Asymmetric Organocatalysis Topics in Current Chemistry Synthesis - Stuttgart Tetrahedron Tetrahedron Journal of Organic Chemistry

2009 2003 2003 2003 2003

291 2 59 59 68

349 247 1599 1805 7098

(55) Suna. E. Mutule. I Microwave methods in organic synthesis Topics in Current Chemistry Synthesis - Stuttgart

2006 2003

226 10

49-101 1610

(56) Zhang, ZC

Advances In Catalysis New Journal Of Chemistry Tetrahedron Letters Tetrahedron

2006 2003 2003 2003

49 27 44 59

153 202 2217 1805

*Cited 51 times in March's Advanced Organic Chemisry, 7th Edition (A copy is enclosed)

List of Publications from 2010-15 as Principal Author (Annex II)

157 Tandem Prins strategy

for the synthesis of spiropyrrolidine and spiropiperidine derivatives

B. V. Subba Reddy,* Y.

Suresh, C. Ravikumar Reddy, M. Rajashekhar Reddy, B. Sridhar

Eur. J. Org. Chem. 2015, DOI:

156 Tandem Prins cyclization for the stereoselective synthesis of 4,5-diaryl-hexahydropyrano [3,4-c]chromene skeleton of calyxins I & J

B. V. Subba Reddy,* M. Ramana Reddy, S. Gopal Reddy, B. Sridhar, and S. Kiran Kumar


155 A novel domino cyclization for the stereoselective synthesis of indeno[2,1-c]pyran and cyclopenta[c]pyran derivatives

B. V. Subba Reddy,* N. Prudhviraju, B. Someswarao, B. J. M. Reddy, B. Sridhar, M. Kanakaraju, A. C. Kunwar

Org. Biomol. Chem., 2015, DOI: 10.1039/C5OB00376H.

154 Stereoselective synthesis of highly functionalized dispirooxindoles through [3+2] cycloaddition of carbonyl ylides with 3-arylidene oxindoles

B. V. Subba Reddy,* Govindaraju Karthik, Tamilselvan Rajasekaran, B. Sridhar

Eur. J. Org. Chem., 2015. DOI: 10.1002/ejoc.201500002

153 Tandem Prins/Wagner/ Ritter process for the stereoselective synthesis of oxabicyclo[4.2.0] octanyl amide and (tetrahydrofuran-3-yl) cyclobutyl)amides

B. V. Subba Reddy,* K. Muralikrishna, N. Jagdeesh Babu, K. Sirisha, A. V. S. Sarma

Org. Biomol. Chem., 2015, 13, under revision.

152 A novel Prins cascade process for the stereoselective synthesis of oxa-bicycles

B. V. Subba Reddy,* A. Venkateswarlu, B. Sridevi, K. Marumudi, A. C. Kunwar, G. Gayathri

Org. Biomol. Chem., 2015, 13, 2669.

151 Sequential glycosylation/ endo-dig cyclization of sugar enynones for the synthesis of pyrano[3,2-c]furan scaffolds

B. V. Subba Reddy,* V. Veerabhadra Reddy, G. Karthik, B. Jagadeesh

Tetrahedron 2015, DOI:10.1016/j.tet.2015.02.089


150 A short and highly

convergent approach for the synthesis of rutaecarpine derivatives

B. V. Subba Reddy,* R. Anji Babu, B. Jagan Mohan Reddy, B. Sridhar, T. R. Murthy, P. Pranathi, S. V. Kalivendi, T. Rao

RSC Advances 2015, 5, 27476.

149 BF3.OEt2-catalyzed synthesis of 1-(tetrahydropyran-3-yl)-1, 3-dihydroisobenzofuran and trans-fused hexahydropyrano[3,2-c]chromene derivatives

B. V. Subba Reddy,* Ch. Syama Sundar, M. Ramana Reddy, B. Sridhar, C. Suresh Reddy

Synthesis-Stuttgart 2015, 46, DOI: 10.1055/s-0034-1380177

148 Bioglycerol derived carbon-SO3H as a recyclable catalyst for the synthesis of tetrahydro-β-carbolines

G. Niranjan Reddy, B. Maheshwar Rao, M. Vijay, B. L. A. P. Devi, R. B. N. Prasad, B. V. Subba Reddy*

Canadian J. Chem., 2015, 93, 341.

147 Friedel-Crafts alkylation of arenes catalyzed by ion-exchange resin: an expedient synthesis of triarylmethanes

B. V. Subba Reddy,* A.Venkateswarlu, B.Sridevi, Salem S. Aldeyab, Ajayan Vinu

J. Nanosci. and Nanotech. DOI:10.1166/jnn.2015.10671

146 Tandem Prins/pinacol

reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds

B. V. Subba Reddy,* S. Gopal Reddy, M. Ramana Reddy, Manika Pal Bhadra, A. V. S. Sarma

Org. Biomol. Chem., 2014, 15, 7257.

145 Stereoselective synthesis of hexahydro-1H-spiro[isoquinoline-4,4 '-pyran] scaffolds through an intramolecular Prins cascade process

B. V. Subba Reddy,* M. Durgaprasad, B. Sridhar

J. Org. Chem. 2015, 80, 653.

144

Stereoselective synthesis of spiro[tetrahydropyran-3,3'-oxindole] derivatives employing Prins cascade strategy

B. V. Subba Reddy,* V. Swathi, Manisha Swain, Manika Pal Bhadra, B. Sridhar, D. Satyanarayana B. Jagadeesh

Organic Letters, 2014, 16, 6267.


143 Intramolecular C-O/C-S bond insertion of a-diazoesters for the synthesis of 2-aryl-4H-benzo[d][1,3]oxazine and 2-aryl-4H-benzo[d][1,3] thiazine derivatives

B. V. Subba Reddy,* R. Anji Babu, M. R. Reddy, B. J. M. Reddy, B. Sridhar

RSC Advances, 2014, 4, 44629.

142 Design, synthesis and anti-mycobacterial activity of 1,2,3,5-tetrasubstituted pyrrolyl-N-acetic acid derivatives

P. L. Reddy, M. Lakshmi Devi, S. Satyanarayana, Ashita Singh, T. Veera Reddy, J. P.Sridevi, G. Raja Sekhar, Yogeeswari, D. Sriram, U. S. Murty, U. Ramesh, B. V. Subba Reddy,* R. Narender

Europran J. Med. Chem. 2014, 84, 118.

141 Aminol initiated Prins

cyclization for the synthesis of octahydro-1H-pyrano[3,4-c] pyridine and hexahydro-1H-furo[3,4-c]pyrrole derivatives

B. V. Subba Reddy,* S. Gopal Reddy, M. Ramana Reddy, B. Sridhar, Manika Pal Bhadra


140 Highly regio-diastereoselective 3CC reaction of donor-acceptor carbenoids for the synthesis of angularly fused furocoumarins/ spirooxindolylfuro coumarins

G. Karthik, T. Rajasekaran, B. Sridhar, B. V. Subba Reddy*

Tetrahedron 2014, 70, 8148.

139 Stereoselective Total Syntheses of Solifenacin and N-Acetyl-1-(4-chloro phenyl)-6,7-dimethoxy tetrahydroisoquinoline

R. Anji Babu, N. Siva Senkar Reddy, B. Jagan Mohan Reddy, B. V. Subba Reddy*

Synthesis-Stuttgart 2014, 46, 2794.

138 Synthesis and biological evaluation of novel pyrano[3,2-c]carbazole derivatives as anti-tumor agents inducing apoptosis via tubulin polymerization inhibition

P. Padmaja, G. Koteswara Rao, A. Indrasena, B. V. Subba Reddy,* N. Patel, A. Basha Shaik, P. Narayana Reddy, Pramod K. Dubey and Manika Pal Bhadra

Org. Biomol. Chem., 2014, 15, 1404.


137 A concise total synthesis

of lyngbic acid, hermitamides A and B

S. Satyanarayana, B V Subba Reddy,* R. Narender


136 Four-Component, One-Pot Synthesis of N-Alkyl-4-oxo-3-phenyl hexahydro-4H-spiro{[1,3]dioxolo[4',5 ':4,5]furo[2,3-f][1,2,3] triazolo[1,5-a][1,4] diazepine-9,1'-cyclo hexane}-6-arboxamides

B. V. Subba Reddy,* Nilanjan Majumder, T. Prabhakar Rao


135 Catalyst and solvent-free cyclopropanation of electron-deficient olefins with cyclic diazoamides for the synthesis of spiro [cyclopropane-1,3 '-indolin]-2 '-one derivatives

G. Karthik, T. Rajasekaran, B. Sridhar, B .V. Subba Reddy*


134 Au(I)/Ag(I)-catalyzed annulation of sugar aldehyde tethered with 3-phenylprop-2-yn-1-yl ether with aryl amines for the pyrano[4,3-b]quinolines

B. V. Subba Reddy,* Nilanjan Majumder, B. Sridhar


133 A new stereoselective total synthesis of phomonol

B. V. Subba Reddy,* L. Srinivas, P. S. K. Reddy, B. P. Reddy, A. R. Prasad, J. S. Yadav

Helvetica Chimica Acta, 2014, 97, 1326.

132 InBr3-Catalyzed

Stereoselective Synthesis of 3,4-Disubstituted Hexahydro-1H-furo[3,4-c]pyran Derivatives

B. V. Subba Reddy,* M. R. Reddy, B. Sridhar, C. S. Reddy


131 A novel Prins reaction for the synthesis of hexahydro-8, 8-dimethyl-1H-isochromen-7-ols

B. V. Subba Reddy,* S. R. Anjum, G.M.Reddy, B. Sridhar



130

Enantioselective 1,4-addition of kojic acid derivatives to beta-nitroolefins catalyzed by a cinchonine derived sugar thiourea

B. V. Subba Reddy,* S. M. Reddy, Manisha Swain

RSC Advances, 2014, 4, 9107.

129 Stereoselective total synthesis of oplopandiol, oploxyne A, and oploxyne B

B. V. Subba Reddy,* R. N. Rao, B. Kumaraswamy, J. S. Yadav


128 Prins Spirocyclization for the Synthesis of Spiro[isobenzofuran-pyran] Derivatives

B. V. Subba Reddy,*

Harish Kumar, P. S. Reddy, S. K. Kumar

Eur. J. Org. Chem., 2014, 4234.

127 Acetal-initiated Prins bicyclization for the synthesis of hexahydrofuro-[3,4-c]furan lignans and octahydropyrano[3,4-c]pyran derivatives

B. V. Subba Reddy,* M. R. Reddy, B. Sridhar,S. K. Kumar

Org. Biomol. Chem., 2014, 12, 4754.

126 o-Benzenedisulfonimide as a recyclable organo catalyst for an efficient and facile synthesis of amidotetrahydropyrans through Prins-Ritter reaction

B. V. Subba Reddy,* Supriya Ghanty

Synthetic Commun. 2014, 44, 2545.

125 B(C6F5)3-catalyzed Prins/Ritter reaction: a novel synthesis of hexahydro-1H-furo[3,4-c]pyranyl amides

B. V. Subba Reddy,* Supriya Ghanty, Ch. Kishore


124 Montmorillonite Clay Catalyzed Three Component, One-Pot Synthesis of 5-Hydroxyindoles

B. V. Subba Reddy,* P. Sivaramakrishna Reddy, Y. Jayasudhan Reddy, N. Bhaskar, and B. Chandra Obula Reddy

Bull. Korean Chem. Soc. 2013, 34, 2968.


123 Prins cascade cyclization for the synthesis of 1,9-dioxa-4-azaspiro[5.5]undecane derivatives

B. V. Subba Reddy,* M. Durgaprasad, B. Sridhar, S. K. Kumar

Journal of Organic Chemistry 2014, 79, 2289.

122 Tuning the reactivity of oxygen/sulfur by acidity of the catalyst in Prins cyclization: oxa- vs thia-selectivity

B. V. Subba Reddy,* A. Venkateswarlu, P. Borkar, J. S. Yadav, B. Sridhar, René Grée


121 InCl3-catalyzed Prins bicyclization for the synthesis of spiro tetrahydropyran derivatives

B. V. Subba Reddy,* S. Jalal, S. K. Kumar

RSC Advances, 2014, 4. 16739.

120 Thee-component, one-pot synthesis of hexahydroazepino[3,4-b]indole and tetrahydro-1H-pyrido[3,4-b]indole derivatives and evaluation of their cytotoxicity

B. V. Subba Reddy,* A. V. Ganesh, M. Vani, T. R. Murthy, S. V. Kalivendi, J. S. Yadav

Bioorganic & Med. Chem. Lett. 2014, 24, 4501.

119 Gold-Catalyzed 5-endo-dig Cyclization of 2-[(2-Aminophenyl)ethynyl]phenylamine with Ketones for the Synthesis of Spiroindolone and Indolo[3,2-c]quinolone Scaffolds

B. V. Subba Reddy,*

Manisha Swain, S. M. Reddy, J. S. Yadav, B. Sridhar

Eur. J. Org. Chem., 2014, 3313.

118 Aza-Ferrier rearrangement of glycals with amides promoted by molecular iodine

Zubeda Begum, Ch. Kishore, V. Veerabhadra Reddy, B. V. Subba Reddy*


117 Stereoselective synthesis

of 2-(2-hydroxyalkyl) piperidine alkaloids through Prins/Ritter reaction

B. V. Subba Reddy,* S. Ghanty, N. S. S. Reddy, Y. J. Reddy, J. S. Yadav



116

115

Ugi three component coupling reaction for the synthesis of 2-(6-oxo-11-phenyl-7,8-dihydrobenzo [b]pyrrolo[1,2-d][1,4] diazocin-5(6H)-yl)-2-phenylacetamides Asymmetric Michael/ hemiketalization of 5-hydroxy-2-methyl-4H-pyran-4-one to β, ¡-unsaturated α-ketoesters catalyzed by a bifunctional rosin-indane amine thiourea catalyst

P. L. Reddy, D. A. Kumar, M. L. Devi, T. V. Reddy , R. Narender, B. V. Subba Reddy*

B. V. Subba Reddy,* Manisha Swain, S. Madhusudana Reddy, J. S. Yadav, B. Sridhar

Tetrahedron Letters, 2014, 55, 657. RSC Advances, 2014, 4, 42299.

114 A convergent and

stereoselective total synthesis of phomolides

B. V. Subba Reddy,* P. S. Reddy, B. P. Reddy, J. S. Yadav

Synlett, 2014, 501.

113 First example of quinine-squaramide catalyzed enantioselective addition of diphenyl phosphite to ketimines

J. George, B. Sridhar, B. V. Subba Reddy*

Org. Biomol. Chem., 2014, 12, 1595.

112 Highly diastereoselective reaction of α-diazoesters with aryl alcohols and isatin imines: Rapid access to oxindole-derived α-alkoxy-beta-amino acids

T. Rajasekaran, G. Karthik, B. Sridhar, S. K. Kumar, B. V. Subba Reddy*

Eur. Journal of Organic Chemistry 2014, 2221.

111 Chemoenzymatic total synthesis of paecilocin A and 3-butyl-7-hydroxyphthalide

Ch. Srilakshmi, A. B. Rao, M. Laxminarsu, B. V. Subba Reddy*


110 A short and efficient synthesis of honokiol via Claisen rearrangement

B. V. Subba Reddy,* R. N. Rao, N. S. Reddy, R. Somaiah, J. S. Yadav, Ravi Subramanyam


109 Stereoselective total synthesis of (+)-boronolide, (+)-anamarine, 8-epi-spicegerolide

B. V. Subba Reddy,* V. V. Reddy, K. Praneeth



108 Stereoselective total

synthesis of penaresidin A starting from D-galactal

B. V. Subba Reddy,* Ch. Kishore, A. S. Reddy



synthesis of almorexant N. S. S. Reddy, B. V.

Subba Reddy*


106 A concise and stereoselective total synthesis of L-783,290

A. S. Reddy, Ch. Kishore, B. V. Subba Reddy*



synthesis of PF 1163A Harish Kumar, A. Srinivas

Reddy, B. V. Subba Reddy*


104 Green Synthesis of

Curcumin Capped Gold Nanoparticles and Evaluation of Their Cytotoxicity

Ch. Sreelakshmi, Nidhi Goel, K. K. R. Datta, A.Anthony, U. Ramesh, B. V. Subba Reddy*

Nanoscience and Nanotechnology Letters, 2013, 5, 1258.

103 Heteropoly acid catalyzed synthesis of 8-methyl-2-aryl/alkyl-3-oxabicyclo [3.3.1]non-7-ene derivatives through (3,5)-oxonium-ene

R. Anjibabu, S. Samaresh, B. J. M. Reddy, B. Rajkumar, B. V. Subba Reddy*


102 Chitosan-SO3H: an efficient, biodegradable, and recyclable solid acid for the synthesis of quinoline derivatives via Friedlander annulation

B. V. Subba Reddy,* A. Venkateswarlu, G. Niranjan Reddy


101 Total synthesis of attenols A and B

B. V. Subba Reddy,* B. P. Reddy, N. Swapnil, J. S. Yadav


100 Montmorillonite clay catalyzed three component, one-pot synthesis of 5-hydroxy indoles

B. V. Subba Reddy,* P. S. Reddy, Y. J. Reddy



synthesis of xyolide B. V. Subba Reddy,* P.

S. Reddy, B. P. Reddy Tetrahedron Letters,

2013, 54, 5758.


98 A concise and convergent

total synthesis of two novel cytotoxic hydro quinones, lanneaquinol and (R)-2 '-hydroxy lanneaquinol

B. V. Subba Reddy,* B. Anusha, U. V. S. Reddy


97 Stereoselective total synthesis of isocladosorpin

B. V. Subba Reddy,* P. J. Reddy, C. Suresh


96 Cellulose-sulfonic acid: An efficient, recyclable, and biodegradable solid acid catalyst for the synthesis of 3-amino alkylindoles

S. Satyanarayana, K. P. Kumar, P. L. Reddy, R. Narender, G. Narasimhulu, B. V. Subba Reddy*

Chemistry Letters 2013, 42, 972.

95 Microwave-assisted cyclocondensation: a rapid and solvent-free synthesis of 3-benzyl-2H-pyrido[1,2-a]pyrimidin-2-one derivatives



94 Stereoselective total synthesis of (+)-8-ethylnorlobelol from anti-1,3-aminoalcohols

B. V. Subba Reddy,* B. P. Reddy, P. S. Reddy, Y. J. Reddy, J. S. Yadav


93 Stereoselective synthesis of hexahydro-1H-pyrano/thiopyrano[3,4-c]quinoline derivatives through a Prins cascade cyclization


Journal of Organic Chemistry, 2013, 78, 8161.

92 A convergent and stereoselective total synthesis of (-)-crispine A, (-)-benzo[a] quinolizidine and (-)-salsolidine

N. S. S. Reddy, B. J. M. Reddy, B. V. Subba Reddy*


91 An expeditious synthesis of 2,3,6-trisubstituted tetrahydropyrans through (3,5)-oxonium-ene cyclization using I2

N. P. Raju, B. J. M. Reddy, R. Anjibabu, B. V. Subba Reddy*



90 Dual behavior of isatin-

based cyclic ketimines with dicarbomethoxy carbene: expedient synthesis of spiro-oxindolyloxazolidines pyrrolines

T. Rajasekaran, G. Karthik, B. Sridhar, B. V. Subba Reddy*


89 Enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone and 1,3-dicarbonyls to β-nitroalkenes catalyzed by a novel bifunctional rosin-indane amine thiourea catalyst

B. V. Subba Reddy,* Manisha Swain, S. M. Reddy

RSC Advances, 2013, 3, 8756.

88 Carbon-SO3H: a novel and recyclable solid acid catalyst for three-component, one-pot synthesis of spiro[4H-pyran-3,3′-oxindoles]

B. M. Rao, G. N. Reddy, T. V. Reddy, B. L. A. P. Devi, R. B. N. Prasad, J. S. Yadav, B. V. Subba Reddy*


87 Cu(OTf)2-catalyzed

synthesis of 2,3-disubstituted indoles and 2,4,5-trisubstituted pyrroles from alpha-diazoketones

B. V. Subba Reddy, M. R. Reddy, Y. G. Rao, J. S. Yadav, B.Sridhar

Organic Letters, 2013 15, 464.

86 Aminoclay-supported copper nanoparticles for 1,3-dipolar cycloaddition of azides with alkynes via Click Chemistry

A. S. Kumar, K. K. R. Datta, T. S. Rao, K. V. Raghavan, M. Eswaramoorthy, B. V. Subba Reddy*

Journal of Nanoscience & Nanotechnology, 2013, 13, 3136.

85 Iron(III)-catalyzed highly efficient, one-pot synthesis of triazolo[1,2-a]indazoletriones and spiro-triazolo[1,2-a] indazoletetraones

B. V. Subba Reddy,* N. Umadevi, G.Narasimhulu, J. S. Yadav


84 Enantioselective Michael reaction of silyl enol ethers to 2-enoylpyridine N-oxides by copper-bis(oxazoline) complex

Jimil George, B. V. Subba Reddy*

Advanced Synthesis & Catalysis, 2013, 355, 383.


83 Prins cascade cyclization

reaction for the synthesis of angularly-fused tetrahydropyran and piperidine derivatives

B. V. Subba Reddy,* Harish Kumar, P.Borkar, J. S. Yadav, B. Sridhar

Eur. J. Org. Chemistry 2013, 1993.

82 Diastereoselective synthesis of 1-(tetrahydrofuran-3-yl)-1,3-dihydroisobenzofuran derivatives via Prins bicyclization

B. V. Subba Reddy,* S. Jalal, P. Borkar, J.S. Yadav, P. G. Reddy, A.V.S. Sarma


81 Polyethylene glycol (PEG-400): a mild and efficient reaction medium for the synthesis of 3-hydroxy-3-(pyridin-2-ylmethyl)indolin-2-ones

M. Raghu, M. Rajasekhar, B. C. O. Reddy, Ch S. Reddy, B. V. Subba Reddy*

Tetrahedron Letters 2013, 54, 3503.

80 A highly stereoselective formal synthesis of hapalosin

Harish Kumar, A. Srinivas Reddy, J. S.Yadav, B. V. Subba Reddy*

Synlett, 2013, 1415.

79 Thia-Prins bicyclization approach for the stereoselective synthesis of dithia- and azathia-bicycles

B. V. Subba Reddy,* A. Venkateswarlu, B. Prashant, J. S. Yadav


78 A novel Prins

bicyclization strategy for the synthesis of sugar annulated furopyran scaffolds

S. Nikhil, P. P. Reddy, B. Sridhar, B. V. Subba Reddy*

Synlett, 2013, 1263.

77 Novel protocol for the

synthesis of octahydro pyrano- and thiopyrano [4,3-a]carbazole derivatives via Prins/ Friedel–Crafts cyclization

B. V. Subba Reddy,* P. S. Reddy, J. S. Yadav, B. Sridhar



76 Sugar thiourea catalyzed highly enantioselective Michael addition of 2-hydroxy-1,4-naphtho-quinone to β-nitroalkenes


RSC Advances 2013, 3, 930.

75 Bismuth(III) Salts as

synthetic tools in organic transforma-tions

J. S. Yadav, A. Antony, B. V. Subba Reddy*

Topics in Current Chemistry, 2012, 311, 229.

74 Gold-Catalyzed domino cycloisomerization/Pictet–Spengler reaction of 2-(4-aminobut-1-yn-1-yl)anilines with aldehydes: synthesis of tetrahydropyrido[4,3-b]indole scaffolds

B. V. Subba Reddy,* Manisha Swain, S. M. Reddy, J. S. Yadav , B. Sridhar

Journal of Organic Chemistry, 2012, 77. 11355.

73 Stereoselective total synthesis of (−)-dihydrotetrabenazine

N. S. S. Reddy, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy*


72 Oxidative C–H functionalization: a novel strategy for the acetoxylation/alkoxylation of arenes tethered to 3,4-dihydroisoquinolines

B. V. Subba Reddy,* N. Umadevi, G. Narasimulu, J.S. Yadav


71 A novel strategy for the chiral 2,4,5-triol moiety and its application to the synthesis of seimatopolide A and (2S,3R,5S)-(−)-2,3-dihydroxy- tetradecan-5- olide

B. P. Reddy, T. Pandurangam, J.S. Yadav, B. V. Subba Reddy*


70 Low-temperature synthesis of pyrano- and furo[3,2-c]quinolines via Povarov reaction using a highly ordered 3D nanoporous catalyst with a high acidity

S. Chauhan, G. P. Mane, C. Anand, D. S. Dhawale, B. V. Subba Reddy,* S. M. J. Zaidi, S. S. Al-Deyab, V. V. B. Subramanian, T. Mori, A. Vinu

Synlett 2012, 2237.


69 Total synthesis of 7-

desmethoxyfusarentin and its methyl ether

P. J. Reddy, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy*


68 First stereoselective total

synthesis of decytospolides A and B

P. J. Reddy, A. S. Reddy, J.S. Yadav, B. V. Subba Reddy*


67 A novel intramolecular

Ugi 3CC for the synthesis of N-alkyl-3-oxo-2-aryl-1,2,3,4-tetrahydropyrazino[1,2-a]indole-1-carboxamides

B. V. Subba Reddy,* S. K. Dey, J. S. Yadav, B. Sridhar


66 Sc(OTf)3/TsOH: a highly efficient catalytic system for the synthesis of 2,6-dioxabicyclo[3,2,1]octane derivatives

B. V. Subba Reddy,* G. Narasimhulu, Y. V. Reddy, P.P. Chakravarthy, J. S. Yadav, B. Sridhar


65 In(OTf)3-catalyzed tandem aza-Piancatelli rearrangement/Michael reaction for the synthesis of 3,4-dihydro-2H-benzo[b][1,4]thiazine and oxazine derivatives

B. V. Subba Reddy,* Y. V. Reddy, P. S. Lakshumma, G. Narasimhulu, J. S. Yadav, B. Sridhar, P. P. Reddy, A. C. Kunwar

RSC Advances 2012, 2, 10661.

64 Stereoselective synthesis of cis-/trans-fused hexahydro pyrano[4,3-b]chromenes via Prins cyclization trapping by a tethered nucleophile

B. V. Subba Reddy,* S.Jalal, P. Borkar, J. S. Yadav, P. P. Reddy, A. C. Kunwar and B. Sridhar

Org. Biomol. Chem., 2012, 10, 6562.

63 Enantioselective Friedel–Crafts alkylation of indoles with 2-enoylpyridine-N-oxides catalyzed by glucoBOX-Cu(II) complex


Org. Biomol. Chem., 2012, 10, 4731.

62 An oxidative Prins & Prins/Friedel-Craftscyclization for the

B. V. Subba Reddy,* P. Borkar, J. S. Yadav, P. P. Reddy, A. C. Kunwar, B.

Org. Biomol. Chem. 2012, 10, 1349.


stereoselective synthesis of dioxabicycles & hexahydro-1H-benzo[f] isochromenes via the benzylic C-H activation

Sridhar, René Grée

61 InCl3-promoted a novel Prins cyclization for the synthesis of hexahydro-1H-furo[3,4-c]pyran derivatives

B. V. Subba Reddy,* M. Sreelatha, Ch. Kishore, P. Borkar, J. S. Yadav


60 A concise total syntheses of (-)-deoxocassine and (-)-deoxoprosophylline from D-xylose

Ch. Kishore, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy*


59

A domino Knoevenagel hetero-Diels-Alder reaction for the synthesis of polycyclic chromene derivatives and evaluation of their cytotoxicity

B. V. Subba Reddy,* B. Divya, Manisha Swain, J. S. Yadav

Bioorg. Med. Chem. Lett. 2012, 22, 1995.

58 A novel tandem ene/Prins cyclization for the synthesis of octahydro pyrano[2,3-c]pyrrole derivatives

B. V. Subba Reddy,* S. R. Anjum, G. M., J. S. Yadav


57 Iodine-catalyzed three-component one-pot synthesis of naphthopyranopyrimidines under solvent-free conditions

K. P. Kumar, S. Satyanarayana, P. L. Reddy, G. Narasimhulu, R.Narender, B. V. Subba Reddy*


56 A concise and diastereoselective synthesis of piperidine and indolizidine alkaloids via aza-Prins cyclization

B. V. Subba Reddy,* D. N. Chaya, J. S.Yadav, René Grée

Synthesis 2012, 297.

55 Gallium(III)-catalyzed

cycloisomerization/Friedel-Crafts alkylation: a facile synthesis of 2,5-disubstituted furans

B. V. Subba Reddy,* B. Bramha Reddy, K. V. R. Rao, J. S. Yadav



54 Pd-Aminoclay Nanocomposite as an Efficient Recyclable Catalyst for Hydrogenation and Suzuki Cross Coupling Reactions


Journal of Nanoscience and Nanotechnology, 2012, 12, 2000.

53

Highly stereoselective cyclopropanation of glycals with cyclic diazoamides: a facile synthesis of spiro oxindolyl sugar derivatives

B. V. Subba Reddy,* T. Rajasekaran, G. Karthik, T. P. Rao


52 A novel sugar based

intramolecular Ugi 3CC for the N-alkyl-3-oxo-4-aryl-octahydrofuro[2,3-f][1,4] oxazepine-5-carboxamides

B. V. Subba Reddy,* N. Majumder, T. P. Rao, B. Sridhar


51 Phosphomolybdic acid: a

highly efficient solid acid for the synthesis of trans-4,5-disubstituted cyclopentenones

B. V. Subba Reddy,* G.Narasimhulu, P. S. Lakshumma, Y. V. Reddy, J. S. Yadav


50 Honey Mediated Green

Synthesis of Pd Nanoparticles for Suzuki Coupling and Hydrogenation of Conjugated Olefins

S. M. Reddy, K. K. R. Datta, Ch. Sreelakshmi, M. Eswaramoorthy, B. V. Subba Reddy*


49 An efficient synthesis of

2-aryl-1,4-diketones via hydroacylation of enones

P. L. Reddy, K. P. Kumar, S. Satyanarayana, R. Narender, B. V. Subba Reddy*


48 Rh2(OAc)4-catalyzed substrate selective [4+2]/[2+2]cycloaddition of acylketenes: a highly chemo-and regioselective synthesis of spiro (oxindolyl)oxazinones and β-lactams

B. V. Subba Reddy,* G. Karthik, T. Rajasekaran, A. Antony, B. Sridhar



47 Quinazolinone-directed

C-H activation: a novel strategy for the acetoxylation/ methoxylation of arenes

B. V. Subba Reddy,* G. Narasimhulu, N. Umadevi, J. S. Yadav

Synlett 2012, 1364

46 1,4-Dipolar cycloaddition reactions in ionic liquids: a facile synthesis of chromenopyridoisoquinolines

B. V. Subba Reddy,* N. N. Yadav, N. Srivastava, J. S. Yadav, B.Sridhar


45 I2-catalyzed condensation

of isatin with indoles: a facile synthesis of di(indolyl)indolin-2-ones and evaluation of their cytotoxicity

B. V. Subba Reddy,* N. Rajeswari, M. Sarangapani, Y. Prashanthi, J. S. Yadav G. R. Jones, A. Anthony


44 Recent Advances in the applications of ionic liquids for the synthesis of bioactive six-membered N-heterocycles


Current Organic Synthesis 2011, 787.

43 BF3.OEt2-Catalyzed

unusual formation of cis-2,3-disubstituted tetrahydrofuran scaffolds

B. V. Subba Reddy,* S. R. Anjum, G. M. Reddy, J. S. Yadav

Synlett, 2011, 2951.

42 Tandem Prins/Friedel-

Crafts cyclization for stereoselective synthesis of heterotricyclic systems

B. V. Subba Reddy,*



41 Regioselective ortho-

acetoxylation/methoxylation of N-(2-benzoylphenyl) benzamides via substrate directed C-H activation

B. V. Subba Reddy,* G. Revathi, A. Srinivas Reddy, J. S. Yadav


40 InBr3-catalyzed three-

component, one-pot synthesis of imidazo[1,2-a]pyridines

B. V. Subba Reddy,* P. Sivaramakrishna Reddy, Y. Jayasudhan Reddy, J. S. Yadav



39 Sc(OTf)3-catalyzed sugar based tandem Ene-Prins cyclization: a novel synthesis of furopyranopyran scaffolds

B. V. Subba Reddy,* A. V. Ganesh, A. Siva Krishna, G. G. K. S. Narayana Kumar, J. S. Yadav


38 Iodine-catalyzed conjugate addition of indoles onto en-1,4-dione: A novel synthesis of 3-(1-(1H-indol-3-yl)-2-oxo-2-phenylethyl)indolin-2-ones as antibacterial and antifungal agents

B. V. Subba Reddy,* N. Rajeswari, M. Sarangapani, G. R. Reddy, Ch. Madan, K. P. Kumar, M. S. Rao

Bioorganic & Medicinal Chemistry Lett. 2011, 21, 6510.

37 CeCl3˙7H2O: A Versatile and Efficient Reagent for the Synthesis of C-Pyrrolyl Glycosides

B. V. Subba Reddy,* Ruchi Jain, K. Bhargavi, Manisha Swain, J. S. Yadav

Synthesis, 2011, 337.

36 Indium(III) Chloride

Catalyzed, Novel and Efficient Synthesis of Sugar Annulated N-Aryltetrahydropyridines

B. V. Subba Reddy,* Ch. D. Vani, Z. Begum, J. S. Yadav, T. P. Rao


35 Recent progress in

transition metal catalysed hydrofunctionalisation of less activated olefins

J. S. Yadav, A. Antony, T. S. Rao, B. V. Subba Reddy*

J. Organomet. Chem., 2011, 696, 16.

34 Quinoxaline-Directed C-

H activation: A novel method for acetoxylation of arenes

B. V. Subba Reddy,* K. Ramesh, J. S. Yadav

Synlett 2011, 169.

33 Triflic acid-promoted

aza-Prins-Ritter reaction sequence: a novel synthesis of 4-amidopiperidine derivatives

B. V. Subba Reddy,* K. Ramesh, A.V. Ganesh, G.G.K.S. N. Kumar, J.S. Yadav, René Grée



32 Iodine-catalyzed

formation of aza-dienes: a novel synthesis of angularly fused hexahydropyrano- and furo[3,2-c]quinoline derivatives

B. V. Subba Reddy,* Harish Grewal


31 Asymmetric Henry reaction catalyzed by a chiral Cu(II) complex: enantioselective synthesis of (S)-2-nitro-1-arylethanols

B. V. Subba Reddy,* S. M. Reddy, Swain Manisha, Ch. Madan

Tetrahedron Asymmetry 2011, 22, 530.

30 Nano Fe3O4 as

magnetically recyclable catalyst for the synthesis of α-aminophos phonates in solvent-free

B. V. Subba Reddy,* A. Siva Krishna, A.V. Ganesh, G.G.K.S.Narayana Kumar


29 NBS or DEAD as

effective reagents in α-thiocyanation of enolizable ketones with ammonium thiocyanate

B. V. Subba Reddy,* S. Madhu Sudana Reddy, Ch. Madan


28 Cellulose-SO3H: an

efficient and biodegradable solid acid for the synthesis of quinazolin-4(1H)-ones

B. V. Subba Reddy,* A. Venkateswarlu, Ch. Madan, A. Vinu


27 A novel trifunctional

organo-catalyst for the asymmetric aldol reaction: a facile enantioselective synthesis of β-hydroxy ketones

B. V. Subba Reddy,* K. Bhavani, A. Raju, J. S. Yadav



synthesis of (-)-cleistenolide

B. V. Subba Reddy,* B. Phaneendra Reddy, T. Pandurangam, J. S. Yadav



25 Indium/Cu(II)-mediated one-pot synthesis of unsymmetri-cal diaryl amines from aryl boronic acids and azides

B. V. Subba Reddy,* N. Sivasankar Reddy, Y. Jayasudhan Reddy, Y. Vikram Reddy


24 1,3-Dipolar cycloaddition of sugar azides with benzyne: a novel synthesis of 1,2,3-benzotriazolyl glycoconjugates

B. V. Subba Reddy,* K. Praneeth, J. S. Yadav

Carbohydrate Research, 2011, 346, 995.

23 BF3·OEt2-catalyzed

tandem Prins Friedel–Crafts reaction: a novel synthesis of sugar fused diaryl hexahydro-2H-furo[3,2-b]pyrans

B. V. Subba Reddy,* Dudhmal N. Chaya, J. S. Yadav, Deepak Chatterjee, A.C. Kunwar


22 Enantioselective Henry reaction catalyzed by a copper(II) glucoBOX complex

B. V. Subba Reddy,* Jimil George

Tetrahedron Asymmetry 2011, 22, 1169

21 Honey Derivatized Au

and Ag Nanoparticles and Evaluation of Its Antimicrobial Activity

Sreelakshmi, Ch.; Datta K. K. R.; Yadav J. S; B. V. Subba Reddy*


20 Palladium(II)-Catalyzed

Auxiliary-Directed C-H Activation for the Regioselective ortho-Arylation of N-(2-Benzoylphenyl) benzamides

B. V. Subba Reddy,* G. Revathi, A. S. Reddy, J. S. Yadav

Synlett, 2011, 2374.

19 Multi-Component

Reactions Using Indium(III) Salts

J. S. Yadav, Aneesh Antony, Jimil George, B. V. Subba Reddy*

Current Organic Chemistry, 2010, 14, 414.

18 Recent Developments in

Indium Metal and Its Salts in Organic Synthesis


European J. Organic Chemistry 2010, 591.

17 HBF4·OEt2 as a mild and

versatile reagent for the B. V. Subba Reddy,* N.

Sivasankar Reddy, Ch. Tetrahedron Letters,

2010, 51, 4827.


Ritter amidation of olefins: a facile synthesis of secondary amides

Madan, J.S. Yadav

16 Nanoporous aluminosilicate catalyst with 3D cage-type porous structure as an efficient catalyst for the synthesis of benzimidazole derivatives

M. A. Chari, D. Shobha, El-Refaie Kenawy, S. S. Al-Deyab, B. V. Subba Reddy,* Ajayan Vinu


15 Efficient Synthesis of 2,3,4-Trisubstituted Quinolines via Friedländer Annulation with Nanoporous Cage-Type Aluminosilicate AlKIT-5 Catalyst

S. Chauhan, R. Chakravarti, S. M. J. Zaidi, S. S. Al-Deyab, B. V. Subba Reddy,* Ajayan Vinu

Synlett, 2010, 2597.

14 Ugi-type four-component

reaction for a novel synthesis of 5-oxo-perhydrofuro[3,2-b]pyran carboxylate derivatives

B. V. Subba Reddy,* N. Majumder, A.V. H.Gopal, D. Chatterjee, A.C. Kunwar


13 Cellulose-SO3H as a recyclable catalyst for the synthesis of tetrahydropyranols via Prins cyclization

B. V. Subba Reddy,* A. Venkateswarlu, G.G.K.S. N. Kumar, A. Vinu


12 Indium(III) chloride catalyzed three-component coupling reaction: A novel synthesis of 2-substituted aryl(indolyl)kojic acid derivatives as potent antifungal and antibacterial agents

B. V. Subba Reddy,* M. R. Reddy, Ch. Madan, K. P. Kumar, M. S. Rao

Bioorganic & Medicinal Chemistry Letters, 2010, 20, 7507.

11 Highly efficient Friedel-

Crafts alkylation of indoles and pyrrole catalyzed by mesoporous 3D aluminosilicate with electron-deficient olefins

T. S. Naidu, V. V. B. Subramanian, M. A. Chari, T. Mori, S. M. J. Zaidi, S. S. Al-Deyab, B. V. Subba Reddy,* A. Vinu

Synlett, 2010, 2813.


10 InCl3-catalyzed three-component reaction: a novel synthesis of dihydropyrano [3,2-b]chromenediones under solvent-free conditions

B. V. Subba Reddy,* M. R. Reddy, G. Narasimhulu, J. S. Yadav


9 Iodine/Et3SiH: a novel

reagent system for the synthesis of 3-aryl-1H-indenes from 1,3-diaryl propargyl alcohols

B. V. Subba Reddy,* B. B. Reddy, K. V. R. Rao, J. S. Yadav


8 Three-Component one-pot synthesis of 3-(2-furanyl)indoles from acetylenedicarboxylate, isocyanide and 3-formyl indole

B. V. Subba Reddy,* A. M. Reddy, D.Somashekar, J. S. Yadav, B. Sridhar


7 Polyethyleneglycol-400 as a Reusable Solvent for 1,4-Dipolar Cycloadditions via Three-Component Reaction

B. V. Subba Reddy,* D. Somashekar, A. M. Reddy, J. S. Yadav, B. Sridhar


6 Highly stereoselective synthesis of 2,3-unsaturated thioglyco-pyranosides employing molecular iodine

B. V. Subba Reddy,* Ch. D. Vani, J. S. Yadav


5 Pd(OAc)2-catalyzed C-H

activation of indoles: a facile synthesis of 3-cyanoindoles

B. V. Subba Reddy,* Z. Begum, Y. J. Reddy, J. S. Yadav


4 Sc(OTf)3-catalyzed

intramolecular aza-Prins- cyclisation for the synthesis of heterobicycles

B. V. Subba Reddy,* P. Borkar, P. P. Chakravarthy, J. S. Yadav, René Grée



3 Novel intramolecular aza-Diels-Alder reaction: a facile synthesis of trans-fused 5H-chromeno[2,3-c]acridine derivatives

B. V. Subba Reddy,* Aneesh Antony, J.S. Yadav


2 3CC reaction of d-

hydroxy-a,b-unsaturated aldehyde, aryl amine and 1,3-diketone: a novel synthesis of oxa-aza bicycles

B. V. Subba Reddy,* Ch. Divyavani, Z. Begum, J. S. Yadav


1 Novel synthesis of tetrahydro-β-carbolines and tetrahydro-isoquinolines via three-component reaction using hexagonally ordered mesoporous AlSBA-15

A. Vinu, P. Kalita, H. Oveisi, M.A.Chari, R.Pal , B. V. Subba Reddy*


List of publications from 2010-15 (Annex III)

226 Tandem Prins strategy

for the synthesis of spiropyrrolidine and spiropiperidine derivatives

B. V. Subba Reddy,* Y.

Suresh, C. Ravikumar Reddy, M. Rajashekhar Reddy, B. Sridhar



B. V. Subba Reddy,*M. Ramana Reddy, S. Gopal Reddy, B. Sridhar, and S. Kiran Kumar


224 A novel domino cyclization for the stereoselective synthesis of indeno[2,1-c]pyran and cyclopenta[c]pyran derivatives

B. V. Subba Reddy,* N. Prudhviraju, B. Someswarao, B. J. M. Reddy, B. Sridhar, M. Kanakaraju, A. C. Kunwar



B. V. Subba Reddy,* Govindaraju Karthik, Tamilselvan Rajasekaran, B. Sridhar

Eur. J. Org. Chem., 2015. DOI: 10.1002/ejoc.201500002

222 Tandem Prins/Wagner/Ritter process for the stereoselective synthesis of oxabicyclo[4.2.0] octanyl amide and (tetrahydrofuran-3-yl) cyclobutyl)amides

B. V. Subba Reddy,* K. Muralikrishna, N. Jagdeesh Babu, K. Sirisha, A. V. S. Sarma



B. V. Subba Reddy,* A. Venkateswarlu, B. Sridevi, Kanakaraju Marumudi, A. C. Kunwar, G. Gayathri

Org. Biomol. Chem., 2015, 13, 2669.


220 Sequential glycosylation/ endo-dig cyclization of sugar enynones for the synthesis of pyrano[3,2-c]furan scaffolds

B. V. Subba Reddy,* V. Veerabhadra Reddy, G. Karthik, B. Jagadeesh

Tetrahedron 2015, 71, DOI: 10.1016/j.tet.2015.02.089

219 A short and highly convergent approach for the synthesis of rutaecarpine derivatives

B. V. Subba Reddy,* R. Anji Babu, B. J. M. Reddy, B. Sridhar, T. R. Murthy, P. Pranathi, S. V. Kalivendi, T. Rao

RSC Advances 2015, 5, 27476.

218 BF3.OEt2-catalyzed synthesis of 1-(tetrahydropyran-3-yl)-1, 3-dihydroisobenzofuran and trans-fused hexahydropyrano[3,2-c]chromene derivatives

B. V. Subba Reddy,* Ch. Syama Sundar, M. Ramana Reddy, B. Sridhar, C. Suresh Reddy

Synthesis-Stuttgart 2015, 46, DOI: 10.1055/s-0034-1380177.


G. N. Reddy, B. M. Rao, M. Vijay, B. L. A. P. Devi, R. B. N. Prasad, B. V. Subba Reddy*

Canadian J. Chem., 2015, 93, 341.


B. V. Subba Reddy,* A.Venkateswarlu,

B.Sridevi, Salem S. Aldeyab, Ajayan Vinu

J. Nanosci. and Nanotech. DOI:10.1166/jnn.2015.10671.

215 Tandem Prins/pinacol

reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds

B. V. Subba Reddy,* S. Gopal Reddy, M. Ramana Reddy, Manika Pal Bhadra, A. V. S. Sarma

Org. Biomol. Chem., 2014, 15, 7257.

214 Stereoselective synthesis of hexahydro-1H-spiro[isoquinoline-4,4'-pyran] scaffolds through Prins cascade process

B. V. Subba Reddy,* M.

Durgaprasad, B. Sridhar J. Org. Chem. 2015,

80, 653.


213


B. V. Subba Reddy,* V. Swathi, Manisha Swain, Manika Pal Bhadra, B. Sridhar, D. Satyanarayana B. Jagadeesh



B. V. Subba Reddy,* R. Anji Babu, M. R. Reddy, B. J. M. Reddy, B. Sridhar

RSC Advances, 2014, 4, 44629.


P. L. Reddy, M. Lakshmi Devi, S. Satyanarayana, A. Singh, T. V. Reddy, J. P. Sridevi, G. Rajasekhar, P.Yogeeswari, D. Sriram, U. S. Murty, U. Ramesh, B. V. Subba Reddy,* R. Narender

Eur J Med Chem. 2014, 84, 118.

210 Aminol initiated Prins

cyclization for the synthesis of octahydro-1H-pyrano[3,4-c]pyridine and hexahydro-1H-furo [3,4-c]pyrrole derivatives

B. V. Subba Reddy,* S. Gopal Reddy, M. Ramana Reddy, B. Sridhar, Manika Pal Bhadra


209 Highly regio- and

diastereoselective 3CC of acyclic/cyclic donor-acceptor carbenoids for the synthesis of fused furocoumarins & spiro oxindolyl furocoumarins

G. Karthik, T. Rajasekaran, B. Sridhar, B. V. Subba Reddy*


208 Stereoselective Total Syntheses of Solifenacin

R. Anji Babu, N. Siva Senkar Reddy, B. Jagan



and N-acetyl-1-(4-chlorophenyl)-6,7-dimethoxytetrahydroisoquinoline

Mohan Reddy, B. V. Subba Reddy*


P. Padmaja, G. Koteswara Rao, A. Indrasena, B. V. Subba Reddy,* N. Patel, A. Basha Shaik, P. N. Reddy, P. K. Dubey, Manika Pal Bhadra

Org. Biomol. Chem., 2014, 15, 1404.

206 A concise total synthesis of lyngbic acid, hermitamides A and B

S. Satyanarayana, B. V. Subba Reddy,* R. Narender


205 Four-Component, one-pot synthesis of N-alkyl-4-oxo-3-phenyl hexahydro-4H-spiro{[1,3]dioxolo [4',5':4,5]furo[2,3-f] [1,2,3]triazolo[1,5-a][1,4] diazepine-9,1'-cyclo hexane}-6-carboxamides

B. V. Subba Reddy,* Nilanjan Majumder, T. Prabhakar Rao


204 Catalyst and solvent-free cyclopropanation of electron-deficient olefins with cyclic diazoamides for the synthesis of spiro [cyclopropane-1,3 '-indolin]-2'-ones

G. Karthik, T. Rajasekaran, B. Sridhar, B .V. Subba Reddy*


203 Au(I)/Ag(I)-catalyzed annulation of sugar aldehyde tethered with 3-phenylprop-2-yn-1-yl ether with aryl amines for the pyrano[4,3-b]quinoline derivatives

B. V. Subba Reddy,* Nilanjan Majumder, B. Sridhar



202 A New Stereoselective

Total Synthesis of Phomonol

B. V. Subba Reddy,* L. Srinivas, P. S. K. Reddy, B. P. Reddy, A. R. Prasad, J. S. Yadav


201 A Formal Synthesis of

Herboxidiene/GEX1A

J. S. Yadav, G. M. Reddy, S. R. Anjum, B. V. Subba Reddy*

Eur. J. Org. Chem. 2014, 4389.

200 InBr3-Catalyzed

Stereoselective Synthesis of 3,4-Disubstituted Hexahydro-1H-furo[3,4-c]pyran Derivatives

B. V. Subba Reddy,* M. R. Reddy, B. Sridhar, C. S. Reddy


199 A novel Prins reaction for

the synthesis of hexahydro-8, 8-dimethyl-1H-isochromen-7-ol derivatives

B. V. Subba Reddy,* S. R. Anjum, G. M.Reddy, B. Sridhar


198


B. V. Subba Reddy,* S.

M. Reddy, Manisha Swain RSC Advances,

2014, 4, 9107.


B. V. Subba Reddy,* R. N. Rao, B. Kumaraswamy, J. S. Yadav


196 Prins spirocyclization for the synthesis of spiro[isobenzofuran-pyran] derivatives

B. V. Subba Reddy,*

Harish Kumar,

P. S. Reddy, S. K. Kumar

Eur. J. Org. Chem., 2014, 4234.



B. V. Subba Reddy,* M. R. Reddy, B. Sridhar,S. K. Kumar

Org. Biomol. Chem., 2014, 12, 4754.

194 A green approach towards the synthesis of enantio pure diols using Horse Radish Peroxidas enzyme immobilized on magnetic nanoparticles

S. S. Deepthi, E. Prasad, B. V. Subba Reddy, B. Sreedhar, A. B. Rao

Green and Sustainable Chemistry, 2014, 4, 15.

193 Stereoselective synthesis of C19-C27 fragment of bryostatin 11

J S Yadav, T. Swamy, B. V. Subba Reddy, V. Ravinder


192 o-Benzenedisulfonimide

as a recyclable homogeneous organocatalyst for an efficient and facile synthesis of 4-amidotetrahydropyran derivatives through prins-ritter reaction

B. V. Subba Reddy,* Supriya Ghanty


191 B(C6F5)3-catalyzed Prins/Ritter reaction: a novel synthesis of hexahydro-1H-furo[3,4-c]pyranyl amide derivatives

B. V. Subba Reddy,* Supriya Ghanty, Ch. Kishore


190 Recent Advancesin Dye Sensitized Solar Cells

U. Mehmood, S. Rahman, K. Harrabi, I. A. Hussein, B. V. Subba Reddy

Advances in Materials Science and Engineering 2014, 1.


189 Montmorillonite Clay Catalyzed Three Component, One-Pot Synthesis of 5-Hydroxyindole Derivatives

B. V. Subba Reddy,* P. Sivaramakrishna Reddy, Y. Jayasudhan Reddy, N. Bhaskar, and B. Chandra Obula Reddy

Bull. Korean Chem. Soc. 2013, 34, 2968

188 Prins cascade

cyclization for the synthesis of 1,9-dioxa-4-azaspiro[5.5]undecane derivatives

B. V. Subba Reddy,* M.

Durgaprasad, B. Sridhar, S. K. Kumar



B. V. Subba Reddy,* A.Venkateswarlu, P.Borkar, J. S. Yadav, B. Sridhar, René Grée


186 Stereoselective synthesis of tetrahydropyran-tetrahydrofuran (THP-THF) core of (+)-muconin via Prins cyclization

J. S. Yadav, U. V. S. Reddy, B. V. Subba Reddy


185 InCl3-catalyzed Prins bicyclization for the synthesis of spirotetrahydropyran derivatives

B. V. Subba Reddy,* S. Jalal, S. K. Kumar

RSC Advances, 2014, 4. 16739.

184 Thee-component, one-pot synthesis of hexahydroazepino [3,4-b]indole and tetrahydro-1H-pyrido[3,4-b]indole derivatives and evaluation of their cytotoxicity

B. V. Subba Reddy,* A. V. Ganesh, M. Vani, T. R. Murthy, S. V. Kalivendi, J. S. Yadav



183 Diastereoselective Synthesis of (+)-Pseudohygroline via Proline-catalyzed alpha-Hydroxylation

B. Anusha, U. V. S. Reddy, B. V. Subba Reddy,* C. S.Reddy

Natural Product Communications, 2014, 9, 633.


B. V. Subba Reddy,*

Manisha Swain, S. M. Reddy, J. S. Yadav, B. Sridhar

Eur. J. Org. Chem., 2014, 3313.


Z. Begum, Ch.Kishore, V. Veerabhadra Reddy, B. V. Subba Reddy*


180 GaCl3-catalyzed activation of alkynyl glycosides for the synthesis of O-glycosides

J. S. Yadav, N. N. Yadav, M. K. Gupta, N. Srivastava, B. V. Subba Reddy

Monatshefte Fur Chemie, 2013, 144, 517.

179 Biogenic preparation of gold nanostructures reduced from Piper longum leaf broth and their electrochemical studies

K. Mallikarjuna, G. Narasimha, N. J. Sushma, G. R. Dillip, B. V. Subba Reddy, B. Sreedhar, B. D. P. Raju


178 Stereoselective total synthesis of 11-methoxycurvularin

J. S. Yadav, Ch. D. Vani, N. Bhasker, B. V. Subba Reddy

Arkivoc, 2014, 291.

177 Stereoselective synthesis of oxylipins, (8R,9R,10S)-trihydroxy octadeca-6Z-enoic acid and (6S,9R,10S)-trihydroxyoctadeca-7E-enoic acid

J. S.Yadav, K. S. Shankar, B. V. Subba Reddy



176 Stereoselective total synthesis of decarestrictine I

J. S. Yadav, M. Venkatesh, A. S. Kumar, P. A. N. Reddy, B. V. Subba Reddy, A. R. Prasad


175 Stereoselective total synthesis of 4-((3S,5R)-3,5-dihydroxy nonadecyl)phenol

J. S. Yadav, P. A.N. Reddy, A. S. Kumar, A. R. Prasad, B. V. Subba Reddy


174 Stereoselective Synthesis of 2-(2-hydroxyalkyl) piperidine alkaloids through Prins/Ritter reaction

B. V. Subba Reddy,* S. Ghanty, N. S. S. Reddy, Y. J. Reddy, J. S. Yadav


173

172

Ugi three-component coupling reaction for the synthesis of 2-(6-oxo-11-phenyl-7,8-dihydrobenzo[b]pyrrolo [1,2-d][1,4]diazocin-5(6H)-yl)-2-phenylacetamide derivatives Asymmetric Michael/hemiketalization of 5-hydroxy-2-methyl-4H-pyran-4-one to beta,gamma-unsaturated alpha-ketoesters catalyzed by a bifunctional rosin-indane amine thiourea catalyst

P. L. Reddy, D. A. Kumar, M. L. Devi, T. V. Reddy ,

R. Narender, B. V. Subba Reddy*

B. V. Subba Reddy,* Manisha Swain, S. Madhusudana Reddy, J. S. Yadav, B. Sridhar

Tetrahedron Letters, 2014, 55, 657. RSC Advances, 2014, 4. 42299.

171 A convergent and

stereoselective total synthesis of phomolides G, H

B. V. Subba Reddy,* P. S. Reddy, B. P. Reddy,

J. S. Yadav

Synlett, 2014, 501.


170 First example of quinine-squaramide catalyzed enantioselective addition of diphenyl phosphite to ketimines derived from isatins

J. George, B. Sridhar, B. V. Subba Reddy*

Org. Biomol. Chem., 2014, 12, 1595.

169 Highly Diastereoselective Reaction of alpha-Diazoesters with Aryl Alcohols and Isatin Imines: Rapid Access to Oxindole-Derived alpha-Alkoxy-beta-amino Acid Derivatives with Two Adjacent Quaternary Carbon Centers

T. Rajasekaran, G. Karthik, B. Sridhar, S. K. Kumar, B. V. Subba Reddy*

Eur. Journal of Organic Chemistry 2014, 2221.


Ch. Srilakshmi, A. B. Rao, M. Laxminarsu, B. V. Subba Reddy*



B. V. Subba Reddy,* R. N. Rao, N.S.Reddy, R. Somaiah, J. S. Yadav, Ravi Subramanyam



B. V. Subba Reddy,* V. V. Reddy, K. Praneeth



synthesis of penaresidin A starting from D-galactal

B. V. Subba Reddy,* Ch. Kishore, A. S. Reddy


164 The stereoselective total synthesis of almorexant

N. S. S. Reddy, B. V. Subba Reddy*




A. S. Reddy, Ch. Kishore, B. V. Subba Reddy*

Tetrahedron Letters, 2014, 55, 5420..


synthesis of PF 1163A Harish Kumar, A. Srinivas

Reddy, B. V. Subba Reddy*


161 Green Synthesis of

Curcumin Capped Gold Nanoparticles and Evaluation of Their Cytotoxicity

Ch. Sreelakshmi, Nidhi Goel, K. K. R. Datta, A. Anthony, U. Ramesh, B. V. Subba Reddy*


160 Heteropoly acid catalyzed synthesis of 8-methyl-2-aryl/alkyl-3-oxa-bicyclo [3.3.1]non-7-ene derivatives through (3,5)-oxonium-ene reaction

R. Anjibabu, S. Samaresh, B. J. M. Reddy, B. Rajkumar, B. V. Subba Reddy*



B. V. Subba Reddy,* A. Venkateswarlu, G. Niranjan Reddy



B. V. Subba Reddy,* B. P. Reddy, N. Swapnil, J. S.Yadav


157 Montmorillonite Clay catalyzed three component, one-pot synthesis of 5-hydroxyindole derivatives

B. V. Subba Reddy,* P. S. Reddy, Y. J. Reddy

Bulletin of the Korean Chemical Society, 2013, 34, 2968.


synthesis of xyolide B. V. Subba Reddy,* P.

S. Reddy, B. P. Reddy Tetrahedron Letters,

2013, 54, 5758.



synthesis of (-)-brevisamide

J. S. Yadav, N. M. Reddy, Md. A. Rahman, B. V. Subba Reddy

Tetrahedron, 2013, 69, 8618.

154

Divergent enantioselective total synthesis of siphonarienal, siphonarienone, and pectinatone

J. S. Yadav, D. N. Chary, N. N. Yadav, B. V. Subba Reddy


153 A Concise and Convergent Total Synthesis of Two Novel Cytotoxic Hydroquinones, Lanneaquinol and (R)-2 '-Hydroxylanneaquinol

B. V. Subba Reddy,* B. Anusha, U. V. S. Reddy


152 A short and facile stereoselective total synthesis of cryptocarya diacetate

J. S. Yadav, P. M. K. Reddy, K. M. Gupta, B. V. Subba Reddy



B. V. Subba Reddy,* P. J. Reddy, C. Suresh







Tetrahedron Letters, 2013, 54, 4892



synthesis of (+)-8-ethylnorlobelol from anti-1,3-aminoalcohols

B. V. Subba Reddy,* B. P. Reddy, P. S. Reddy, Y. J. Reddy, J. S. Yadav


147 Stereoselective synthesis of hexahydro-1H-pyrano/thiopyrano [3,4-c]quinoline derivatives through a Prins cascade cyclization



146 A convergent and stereoselective total synthesis of (-)-crispine A, (-)-benzo[a]quinolizidine and (-)-salsolidine

N. S. S. Reddy, B. J. M. Reddy, B. V. Subba Reddy*


145 A simple and expeditious synthesis of 2,3,6-trisubstituted tetrahydropyrans through (3,5)-oxonium-ene cyclization using molecular iodine

N. P. Raju, B. J. M. Reddy, R. Anjibabu, B. V. Subba Reddy*


144 Dual behavior of isatin-based cyclic ketimines with dicarbomethoxy carbene: expedient synthesis of highly functionalizedspirooxindolyl oxazolidines and pyrrolines

T. Rajasekaran, G. Karthik, B. Sridhar, B. V. Subba Reddy*


143 Enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone and 1,3-dicarbonyls to β-nitroalkenes catalyzed by

B. V. Subba Reddy,* Manisha Swain, S. M. Reddy

RSC Advances, 2013, 3, 8756.


a novel bifunctional rosin-indane amine thiourea catalyst


B. M. Rao, G. N. Reddy, T. V. Reddy, B. L. A. P. Devi, R. B. N. Prasad, J. S. Yadav, B. V. Subba Reddy*



of anti-1,3-aminoalcohols via reductive opening of 4-amido tetrahydropyrans derived from the Prins/Ritter sequence

J. S. Yadav, Y. J. Reddy, P. A. N. Reddy, B. V. Subba Reddy


140 Cu(OTf)2-catalyzed synthesis of 2,3-disubstituted indoles and 2,4,5-trisubstituted pyrroles from alpha-diazoketones

B. V. Subba Reddy,* M. R. Reddy, Y. G. Rao, J. S. Yadav, B.Sridhar





138 Iron(III)-catalyzed highly efficient, one-pot synthesis of triazolo[1,2-a]indazoletriones and spiro-triazolo[1,2-a] indazoletetraones

B. V. Subba Reddy,* N. Umadevi, G.Narasimhulu, J. S. Yadav


137 Enantioselective Michael reaction of silyl enol ethers to 2-enoylpyridine N-oxides catalyzed by copper-bis(oxazoline)




136 Prins cascade cyclization

reaction for the synthesis of angularly-fused tetrahydropyran and piperidine derivatives

B. V. Subba Reddy,* Harish Kumar, P.Borkar, J. S. Yadav, B. Sridhar

Eur. J. Org. Chemistry., 2013, 1993.


B. V. Subba Reddy,* S. Jalal, P. Borkar, J.S. Yadav, P. G. Reddy, A.V.S. Sarma


134 SN2 substitution reaction of 2-C-acetoxymethyl glycals catalyzed by iodine: a novel synthesis of 2-C-N-arylamidomethyl glycals

J. S. Yadav, G. Narasimhulu, N. Umadevi, Y. V. Reddy, B. V. Subba Reddy



M. Raghu, M. Rajasekhar, B. C. O. Reddy, Ch S. Reddy, B. V. Subba Reddy*

Tetrahedron Letters 2013, 54, 3503


Harish Kumar, A. Srinivas Reddy, J. S. Yadav, B. V. Subba Reddy*

Synlett, 2013, 1415.


B. V. Subba Reddy,* A. Venkateswarlu, B. Prashant, J. S. Yadav


130 A formal stereoselective synthesis of (-)-brevisamide

J.S.Yadav, A.Raju, K. Ravindar, B. V. S. Reddy



129 A novel Prins bicyclization strategy for the synthesis of sugar annulated furopyran scaffolds

S. Nikhil, P. P. Reddy, B. Sridhar, B. V. Subba Reddy*

Synlett, 2013, 1263.

128 Solvent-free cyanoethylation of selected alcohols using Amberlyst A-21 polymer resin

M. Trinadh, T. Rajasekhar, B. Bhadru, J. Gopinath, V. Santosh, B. V. Subba Reddy, A.V.S. Sainath

J. Appl. Polym. Sci. 2013, 128, 795.

127 Novel protocol for the synthesis of octahydropyrano- and thiopyrano [4,3-a]carbazole derivatives via Prins/Friedel–Crafts cyclization

B. V. Subba Reddy,* P. S. Reddy, J. S. Yadav, B. Sridhar


126 Sugar thiourea catalyzed highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone to β-nitroalkenes



125 Copper salt of 12-tungstophosphoric acid: an efficient and reusable heteropoly acid for the Click Chemistry

K. V. Purnima, D. Sreenu, N. Bhasker, K. Nagaiah, N. Lingaiah, B. V. Subba Reddy, J. S. Yadav

Chinese. J. Chem. 2013, 31, 534.

124 Bismuth(III) Salts as synthetic tools in organic transforma-tions




123 Gold-Catalyzed domino cycloisomerization/Pictet–Spengler reaction of 2-(4-aminobut-1-yn-1-yl)anilines with aldehydes: synthesis of tetrahydropyrido[4,3-b] indole scaffolds

B. V. Subba Reddy,* Manisha Swain, S. M. Reddy, J. S. Yadav , B. Sridhar



N. S. S. Reddy, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy*


121 Stereoselective total synthesis of (3R,5R)-sonnerlactone and (3R,5S)-sonnerlactone

J. S. Yadav, K. S. Shankar, A. S. Reddy, B. V. Subba Reddy


120 Synthetic studies toward potent cytostatic macrolide bryostatin: an expedient synthesis of C1–C10 fragment

J.S. Yadav, S. Aravind, G. M. Kumar, B. V. Subba Reddy


119 The first stereoselective total synthesis of the Z-isomer of cytospolide E

J. S. Yadav, T. Pandurangam, A. S. Kumar, P.A.N.Reddy, A.R. Prasad, B. V. Subba Reddy, K. R. Prasad, A.C. Kunwar



B. V. Subba Reddy,* N. Umadevi, G. Narasimulu, J.S. Yadav


117 A novel strategy for the chiral 2,4,5-triol moiety and itsapplication to the synthesis of

B. P. Reddy, T. Pandurangam, J. S. Yadav, B. V. Subba Reddy*



seimatopolide A and (2S,3R,5S)-(−)-2,3-dihydroxy- tetradecan-5- olide

116 Studies directed towards the synthesis of bryostatin: a stereoselective synthesis of the C7-C16 fragment

J. S. Yadav, S. Aravind, G. M. Kumar, B. V. Subba Reddy



S. Chauhan, G. P. Mane, C. Anand, D. S. Dhawale, B. V. Subba Reddy,* S. M. J. Zaidi, S. S. Al-Deyab, V. V. B. Subramanian, T. Mori, A. Vinu

Synlett 2012, 2237.

114 Total synthesis of 7-desmethoxyfusarentin and its methyl ether

P. J. Reddy, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy*


113 First stereoselective total synthesis of decytospolides A and B

P. J. Reddy, A. S. Reddy, J.S. Yadav, B. V. Subba Reddy*


112 A novel intramolecular

Ugi 3CC for the synthesis of N-alkyl-3-oxo-2-aryl-1,2,3,4-tetrahydropyrazino [1,2-a]indole-1-carboxamides

B. V. Subba Reddy,* S. K. Dey, J. S. Yadav, B. Sridhar



B. V. Subba Reddy,* G. Narasimhulu, Y. V. Reddy, P.P. Chakravarthy, J. S. Yadav, B. Sridhar



110 In(OTf)3-catalyzed tandem aza-Piancatelli rearrangement/Michael reaction for the synthesis of 3,4-dihydro-2H-benzo[b][1,4]thiazine and oxazine derivatives

B. V. Subba Reddy,* Y. V. Reddy, P. S. Lakshumma, G. Narasimhulu, J. S. Yadav, B. Sridhar, P. P. Reddy, A. C. Kunwar

RSC Advances 2012, 2, 10661.

109 Unprecedented

synergistic effects between weak Lewis and Brønsted acids in Prins cyclization

P. Borkar, P.van de Weghe, B. V. Subba Reddy, J. S. Yadav, René Grée

Chem. Commun. 2012, 48, 9316.


B. V. Subba Reddy,* S.Jalal, P. Borkar, J. S. Yadav, P. P. Reddy, A. C. Kunwar and B. Sridhar

Org. Biomol. Chem., 2012, 10, 6562.



Org. Biomol. Chem., 2012, 10, 4731.

106 An oxidative Prins & Prins/Friedel-Craftscyclization for the stereoselective synthesis of dioxabicycles & hexahydro-1H-benzo[f] isochromenes via the benzylic C-H activation

B. V. Subba Reddy,* P. Borkar, J. S. Yadav, P. P. Reddy, A. C. Kunwar, B. Sridhar, René Grée

Org. Biomol. Chem. 2012, 10, 1349.


B. V. Subba Reddy,* M. Sreelatha, Ch. Kishore, P. Borkar, J. S. Yadav



104 A concise total syntheses of (-)-deoxocassine and (-)-deoxoprosophylline from D-xylose

Ch. Kishore, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy*


103


B.V. Subba Reddy,* B. Divya, Manisha Swain, J. S. Yadav

Bioorg. Med.Chem. Lett. 2012, 22, 1995.

102 A novel tandem ene/Prins cyclization for the synthesis of octahydropyrano[2,3-c]pyrrole derivatives

B. V. Subba Reddy,* S. R. Anjum, G. M., J. S. Yadav



K. P. Kumar, S. Satyanarayana, P. L. Reddy, G. Narasimhulu, R.Narender, B. V. Subba Reddy*


100 Chemoenzymatic approach for the total synthesis of (+)-bourgeanic acid

J. S. Yadav, T. S. Rao, N. N. Yadav, K. V. R.Rao, B. V. Subba Reddy, A. K. Ghamdi


99 Total synthesis of (-)-pyrenophorol

J. S. Yadav, G. M. Reddy, T. S. Rao, B. V. Subba Reddy, A. K. Ghamdi



of (4S,6S)-6-hydroxy-4-undeca-nolide: A Pheromone of the Giant White Butterfly Idea Leuconoe

J. S. Yadav, P.A.N. Reddy, Hissana Ather, A. S. Kumar, A. R. Prasad, B. V. Subba Reddy




B. V. Subba Reddy,* D. N. Chaya, J. S.Yadav, René Grée



synthesis of putaminoxin J. S. Yadav, A. Raju, K.

Ravindar, B. V. Subba Reddy


95 Gallium(III)-catalyzed cycloisomerization/Friedel-Crafts alkylation: a facile synthesis of 2,5-disubstituted furans

B. V. Subba Reddy,* B. Bramha Reddy, K. V. R. Rao, J. S. Yadav


94 Pd-Aminoclay

Nanocomposite as an Efficient Recyclable Catalyst for Hydrogenation and Suzuki Cross Coupling Reactions



93


B. V. Subba Reddy,* T. Rajasekaran, G. Karthik, T. P. Rao


92 A novel sugar based

intramolecular Ugi 3CC for the N-alkyl-3-oxo-4-aryl-octahydrofuro[2,3-f][1,4] oxazepine-5-carboxamides

B. V. Subba Reddy,* N. Majumder, T. P. Rao, B. Sridhar


91 Phosphomolybdic acid: a

highly efficient solid acid for the synthesis of trans-4,5-disubstituted

B. V. Subba Reddy,* G.Narasimhulu, P.S. Lakshumma, Y. V. Reddy, J. S. Yadav



cyclopentenones

90 Honey Mediated Green Synthesis of Pd Nanoparticles for Suzuki Coupling and Hydrogenation of Conjugated Olefins

S. M. Reddy, K. K. R. Datta, Ch. Sreelakshmi, M. Eswaramoorthy, B. V. Subba Reddy*

Nanoscience and Nanotechnology Letters, 2012, 4, 420

89 An efficient synthesis of

2-aryl-1,4-diketones via hydroacylation of enones

P. L. Reddy, K. P. Kumar, S. Satyanarayana, R. Narender, B. V. Subba Reddy*


88 Rh2(OAc)4 catalyzed substrate selective [4+2]/[2+2] cycloaddition of acyl ketenes: a highly chemo- and regioselective synthesis of spiro (oxindolyl)oxazinones and β-lactams

B. V. Subba Reddy,* G. Karthik, T. Rajasekaran, A. Antony, B. Sridhar


87 Quinazolinone-directed C-H activation: a novel strategy for the acetoxylation /methoxylation of arenes

B. V. Subba Reddy,* G. Narasimhulu, N. Umadevi, J. S. Yadav

Synlett 2012, 1364


B. V. Subba Reddy,* N. N. Yadav, N. Srivastava, J. S. Yadav, B.Sridhar


85 Iodine-catalyzed

condensation of isatin with indoles: a facile synthesis of di(indolyl)indolin-2-ones and evaluation of their cytotoxicity

B. V. Subba Reddy,* N. Rajeswari, M. Sarangapani, Y. Prashanthi, J. S. Yadav G. R. Jones, A. Anthony



84 Recent Advances in the

Applications of Ionic Liquids for the Synthesis of Bioactive Six-Membered N-Heterocycles



83 BF3.OEt2-Catalyzed

Unusual Formation of cis-2,3-Disubstituted Tetrahydrofuran Scaffolds

B. V. Subba Reddy,* S. R. Anjum, G. M. Reddy, J. S. Yadav

Synlett, 2011, 2951.

82 Tandem Prins/Friedel-

Crafts Cyclization for Stereoselective Synthesis of Heterotricyclic Systems

B. V. Subba Reddy,*



81 Regioselective ortho-

acetoxylation/methoxylation of N-(2-benzoylphenyl) benzamides via substrate directed C-H activation

B. V. Subba Reddy,* G. Revathi, A. Srinivas Reddy, J. S. Yadav


80 InBr3-catalyzed three-

component, one-pot synthesis of imidazo[1,2-a]pyridines

B. V. Subba Reddy,* P. Sivaramakrishna Reddy, Y. Jayasudhan Reddy, J. S. Yadav


79 Stereoselective total synthesis of (+)-18-(6S,9R,10R)-bovidic acid

J. S. Yadav, K. Ramesh, U. V. Subba Reddy, B. V. Subba Reddy, A. K. Ghamdi


78 First stereoselective total

synthesis and biological evaluation of Amphidinin B and its analogues

J. S. Yadav, A. Srinivas Reddy, Ch. Suresh Reddy, B. V. Subba Reddy,* S. Venkateshwarlu, A. Anthony

European Journal of Organic Chemistry 2011, 696.



B. V. Subba Reddy,* A. V. Ganesh, A. Siva Krishna, G. G. K. S. Narayana Kumar, J. S. Yadav


76 Total synthesis of

cryptophycin-24 (arenastatin A) via Prins cyclization

J.S. Yadav, K.V. Purnima, B. V. Subba Reddy, K. Nagaiah, A.K. Ghamdi


75 Iodine-catalyzed

conjugate addition of indoles onto en-1,4-dione: a novel synthesis of 3-(1-(1H-indol-3-yl)-2-oxo-2-phenylethyl) indolin-2-ones as antibacterial/antifungal agents

B. V. Subba Reddy,* N. Rajeswari, M. Sarangapani, G. R. Reddy, Ch. Madan, K. P. Kumar, M. S. Rao



B. V. Subba Reddy,* Ruchi Jain, K. Bhargavi, Manisha Swain, J. S. Yadav


73 Indium(III) Chloride

Catalyzed, Novel and Efficient Synthesis of Sugar Annulated N-Aryltetrahydropyridines

B. V. Subba Reddy,* Ch. D. Vani, Z. Begum, J. S. Yadav, T. P. Rao


72 Recent progress in

transition metal catalyzed hydrofunctionalisation of less activated olefins

J. S. Yadav, A. Antony, T. S. Rao, B. V. Subba Reddy*


71 Green Synthesis Of Silver Nanoparticles Using Ocimum Leaf Extract And Their Characterization

K.Mallikarjuna, G. Narasimha, G.R.Dillip, B. Praveen, B.Sreedhar, C.Sreelakshmi, B. V. Subba Reddy,* B. D. Prasad Raju

Digest J. Nanomaterials and Biostructures, 2011, 6, 181.


70 Total synthesis of (+)-

Bourgeanic acid utilizing Desymmetrization strategy

J. S. Yadav, K. V. R.Rao, K. Ravindar, B. V. Subba Reddy*


69 Quinoxaline-Directed C-H activation: A novel method for acetoxylation of arenes

B. V. Subba Reddy,* K. Ramesh, J. S. Yadav

Synlett 2011, 169.

68 Triflic acid-promoted

aza-Prins-Ritter reaction sequence: a novel synthesis of 4-amidopiperidine derivatives

B. V. Subba Reddy,* K. Ramesh, A.V. Ganesh, G.G.K.S. N. Kumar, J.S. Yadav, René Grée


67 Iodine-catalyzed

formation of aza-dienes: a novel synthesis of angularly fused hexahydropyrano- and furo[3,2-c]quinoline derivatives

B. V. Subba Reddy,* Harish Grewal



B. V. Subba Reddy,* S. M. Reddy, Swain Manisha, Ch. Madan


65 Nano Fe3O4 as

magnetically recyclable catalyst for the synthesis of α-aminophos phonates in solvent-free

B. V. Subba Reddy,* A. Siva Krishna, A.V. Ganesh, G.G.K.S. Narayana Kumar


64 NBS or DEAD as

effective reagents in α-thiocyanation of enolizable ketones with ammonium thiocyanate

B. V. Subba Reddy,* S. Madhu Sudana Reddy, Ch. Madan



63 Cellulose-SO3H: an

efficient and biodegradable solid acid for the synthesis of quinazolin-4(1H)-ones

B. V. Subba Reddy,* A. Venkateswarlu, Ch. Madan, A. Vinu


62 A novel trifunctional

organo-catalyst for the asymmetric aldol reaction: a facile enantioselective synthesis of β-hydroxy ketones

B. V. Subba Reddy* K. Bhavani, A. Raju, J. S. Yadav



synthesis of (-)-cleistenolide

B. V. Subba Reddy,* B. Phaneendra Reddy, T. Pandurangam, J. S. Yadav


60 Indium/Cu(II)-mediated

one-pot synthesis of unsymmetri-cal diaryl amines from aryl boronic acids and azides

B. V. Subba Reddy,* N. Sivasankar Reddy, Y. Jayasudhan Reddy, Y. Vikram Reddy



B. V. Subba Reddy,* K. Praneeth, J. S. Yadav


58 BF3·OEt2-catalyzed

tandem Prins Friedel–Crafts reaction: a novel synthesis of sugar fused diaryl hexahydro-2H-furo[3,2-b]pyrans

B. V. Subba Reddy,* Dudhmal N. Chaya, J. S. Yadav, Deepak Chatterjee, A.C. Kunwar



B. V. Subba Reddy,* Jimil George



56 Sodium borohydride/

methoxydiethylborane mediated syn-1,3-stereoselective total synthesis of Herbarumin-III

J S Yadav, G. Narasimhulu, Y. V. Reddy, B. V. Subba Reddy

Indian Journal of Chemistry, Section B: Organic Chemistry, 2011, 50, 1075.

55 Enantioselective Total

Synthesis of (+)-Vittatalactone

J. S. Yadav, N. N. Yadav, T. S. Rao, B. V. Subba Reddy, A. A. Ghamdi


54 Honey Derivatized Au

and Ag Nanoparticles and Evaluation of Its Antimicrobial Activity

Sreelakshmi, Ch.; Datta K. K. R.; Yadav J. S; B. V. Subba Reddy*


53 Palladium(II)-Catalyzed

Auxiliary-Directed C-H Activation for the Regioselective ortho-Arylation of N-(2-Benzoylphenyl) benzamides

B. V. Subba Reddy,* G. Revathi, A. S. Reddy, J. S. Yadav

Synlett, 2011, 2374.

52 Concise Total Synthesis

of (-)-cis-Aerangis Lactone and (-)-cis-Cognac Lactone

J. S. Yadav, R. N. Rao, B. P. Kumar, R. Somaiah, B. V. Subba Reddy


51 A practical synthesis of

bis(indolyl)methanes employing boric acid

J. S. Yadav, M. K. Gupta, Ruchi Jain, N. N. Yadav, B. V. Subba Reddy

Monatshefte Fur Chemie, 2010, 141,1001.

50 Stereoselective Total

Synthesis of Leiocarpin C and (+)-Goniodiol

J. S. Yadav, V. Hari Krishna, A. Srilatha, R. Somaiah, B. V. Subba Reddy


49 Multi-Component

Reactions Using Indium(III) Salts




48 Recent Developments in Indium Metal and Its Salts in Organic Synthesis



47 Gold Nanoparticles Embedded in a Mesoporous Carbon Nitride Stabilizer for Highly Efficient Three-Component Coupling Reaction

K. K. R. Datta, B. V. Subba Reddy,* K. Ariga, Ajayan Vinu

Angew. Chem. Int. Engl. Ed., 2010, 49, 5961.

46 Samarium triflate as mild

and efficient catalyst for aza-Diels-Alder reaction: A facile synthesis of cis-fused pyrano- and furanoquinolines

A. Venkat Narsaiah, A. Ramesh Reddy, B. V. Subba Reddy, J. S. Yadav


45 HBF4·OEt2 as a mild and

versatile reagent for the Ritter amidation of olefins: a facile synthesis of secondary amides

B. V. Subba Reddy,* N. Sivasankar Reddy, Ch. Madan, J.S. Yadav



M. A. Chari, D. Shobha, El-Refaie Kenawy, S. S. Al-Deyab, B. V. Subba Reddy,* Ajayan Vinu


43 Efficient Synthesis of 2,3,4-trisubstituted quinolines via Friedländer annulation with nanoporous cage-type aluminosilicate AlKIT-5 catalyst

S. Chauhan, R. Chakravarti, S. M. J. Zaidi, S. S. Al-Deyab, B. V. Subba Reddy,* Ajayan Vinu

Synlett, 2010, 2597.


42 Ugi-type four-component reaction for a novel synthesis of 5-oxo-perhydrofuro[3,2-b]pyran carboxylate derivatives

B. V. Subba Reddy,* N. Majumder, A.V. H.Gopal, D. Chatterjee, A.C. Kunwar



B. V. Subba Reddy,* A. Venkateswarlu, G.G.K.S. N. Kumar, A. Vinu


40 Indium(III) chloride catalyzed 3CC reaction: a novel synthesis of 2-substituted aryl(indolyl) kojic acid derivatives as potent antifungal & antibacterial agents

B. V. Subba Reddy,* M. R. Reddy, Ch. Madan, K. P. Kumar, M. S. Rao


39 A practical total synthesis of (+)-Spirolaxine methyl ether

J. S. Yadav, M. Sreenivas, A. S. Reddy, B. V. Subba Reddy



Rhoiptelol B J. S. Yadav, T.

Pandurangam, V. V. B. Reddy, B. V. Subba Reddy


37 Highly Efficient Friedel-

Crafts Alkylation of Indoles and Pyrrole Catalyzed by Mesoporous 3D Aluminosilicate Catalyst with Electron-Deficient Olefins

T. S. Naidu, V. V. B. Subramanian, M. A. Chari, T. Mori, S. M. J. Zaidi, S. S. Al-Deyab, B. V. Subba Reddy,* A. Vinu

Synlett, 2010, 2813.

36 Stereoselective Total

Synthesis of (3R,5R)-5-Hydroxy-de-O-methyllasiodiplodin via the Prins Cyclization

J. S. Yadav, N. Thrimurtulu, Md. Ataur Rahman, J. S. Reddy, A. R. Prasad, B. V. Subba Reddy



35 InCl3-catalyzed three-

component reaction: a novel synthesis of dihydropyrano[3,2-b] chromenediones under solvent-free conditions

B. V. Subba Reddy,* M. R. Reddy, G. Narasimhulu, J. S. Yadav


34 Stereoselective total synthesis of (+)-garvensintriol

J.S. Yadav, U.V. S. Reddy, B. Anusha, B. V. Subba Reddy


33 Iodine/Et3SiH: a novel

reagent system for the synthesis of 3-aryl-1H-indenes from 1,3-diaryl propargyl alcohols

B. V. Subba Reddy,* B. B. Reddy, K. V. R. Rao, J. S. Yadav



B. V. Subba Reddy,* A. M. Reddy, D.Somashekar, J. S. Yadav, B. Sridhar


31 Polyethyleneglycol-400 as a reusable solvent for 1,4-dipolar cycloaddition via three-component reaction

B. V. Subba Reddy,* D. Somashekar, A. M. Reddy, J. S. Yadav, B. Sridhar



B.V.Subba Reddy,* Ch. D. Vani, J. S. Yadav


29 Pd(OAc)2-catalyzed C-H

activation of indoles: a facile synthesis of 3-cyanoindoles

B. V. Subba Reddy,* Z. Begum, Y. J. Reddy, J. S. Yadav



28 Sc(OTf)3-catalyzed intramolecular aza-Prins- cyclisation for the synthesis of heterobicycles

B. V. Subba Reddy,* P. Borkar, P. P. Chakravarthy, J. S. Yadav, René Grée


27 Novel intramolecular

aza-Diels-Alder reaction: a facile synthesis of trans-fused 5H-chromeno[2,3-c]acridine derivatives

B. V. Subba Reddy,* Aneesh Antony, J.S. Yadav


26 Iodine as a versatile catalyst for the hydroalkylation of vinyl arenes with 1,3-diketones

J.S. Yadav, B. V. Subba Reddy, T. S. Rao, K. Bhavani, A. Raju


25 HBF4.OEt2 as a versatile reagent for the Hosomi-Sakurai allylation and Prins cyclisation: one-pot synthesis of symmetrical 4-fluoro tetrahydropyrans

J. S. Yadav, B. V. Subba Reddy, B. Anusha, U. V. S. Reddy, V. V. B. Reddy.


24 Substrate-controlled

stereoselective synthesis of Ophiocerin C

J. S. Yadav, N. R. Reddy, B. B. M. Krishna, Ch. V. Vardhan, B. V. Subba Reddy



Aculeatins A and B from L-malic acid

J. S. Yadav, Y. Gopala Rao, D. Chandrakanth, K. Ravindar, B. V. Subba Reddy


22 Versatile intramolecular

aza-Prins and Prins cyclization of aryl epoxides: a novel synthesis of diaza-,oxa-aza- and dioxa-bicycles

J.S.Yadav, P. Borkar, P. P. Chakravarthy, B. V. Subba Reddy, A. V. S. Sarma, B. Sridhar, René Grée



21 Stereoselective total synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one via Prins cyclisation

J. S. Yadav, D. Chandrakanth , Y. G. Rao, K. Ravindar, B. V. Subba Reddy


20 Sc(OTf)3-catalysed one-pot Ene-Prins cyclization: a novel synthesis of octahydro-2H-chromen-4-ols

J. S. Yadav, B. V. Subba Reddy, A. V. Ganesh, G. G. K. S. N. Kumar


19 Allylic nucleophilic

substitution of Morita-Baylis-Hillman acetates with isocyanides: a facile synthesis of trisubstituted olefins

J. S. Yadav, B. V. Subba Reddy, A. P. Singh, N. Majumdar


18 Domino Knoevenagel-

hetero-Diels-Alder reactions: a stereoselective synthesis of sugar annulated furo[3,2-b]pyrano[4,3-d]pyrans

J. S. Yadav, B. V. Subba Reddy, A.V. H. Gopal, R. N. Rao, R. Somaiah, P. P. Reddy, A. C. Kunwar


17 Total synthesis of (+)-pseudohygroline

J. S. Yadav, G. Narasimhulu, N. M. Reddy, B. V. Subba Reddy


16 Stereoselective total synthesis of 11-α-methoxy curvularin and 11-β-methoxy curvularin

J. S. Yadav, A. Raju, K. Ravindar, B. V. Subba Reddy


15 Stereoselective Synthesis

of (10S,12S)-10-hydroxy-12-methyl-1-oxacyclo dodecane-2,5-dione via Prins cyclisation

J. S. Yadav, N. Thrimurtulu, M. Venkatesh, K. V. R. Rao, A. R., Prasad, B. V. Subba Reddy



14 An expeditious synthesis

of 4-fluoropiperidines via aza-Prins cyclization

J. S. Yadav, B. V. Subba Reddy, K. Ramesh, G. G. K. S. N. Kumar, René Grée


13 Total synthesis of (+)-Aculeatin D and (+)-6-epi-Aculeatin D

J. S. Yadav, K. V. R. Rao, K. Ravindar, B. V. Subba Reddy

Synlett. 2010, 51.

12 Stereoselective total synthesis of (–)-Ovalicin

J. S. Yadav, P. N. Reddy, B. V. Subba Reddy

Synlett. 2010, 457.

11 3CC reaction of d-hydroxy-a,b-unsaturated aldehyde, aryl amine and 1,3-diketone: a novel synthesis of oxa-aza bicycles

B. V. Subba Reddy,* Ch. Divyavani, Z. Begum, J. S. Yadav


10 Stereoselective total synthesis of Goniothalesdiol A via Chiron approach

J. S. Yadav, R. N. Rao, R. Somaiah, V. Harikrishna, B. V. Subba Reddy

Helvetica Chimica Acta, 2010, 1362.


synthesis of decarestrictine-J via Ring Closing Metathesis

J. S. Yadav, K. A. Lakshmi, N. M. Reddy, A. R. Prasad, B. V. Subba Reddy


8 First example of

carbohydrate based Prins cyclization: a novel class of sugar annulated tetrahydropyrans

J. S. Yadav, B. V. Subba Reddy, A. P. Singh, D. N.Chaya, D. Chatterjee, A. C. Kunwar


7 First example of FeCl3-

catalyzed alkylation of indoles with pinenes

J. S. Yadav, B. V. Subba Reddy, G. Narasimhulu, N. S. Reddy, P. N. Reddy, K.V. Purnima, P. Naresh, B. Jagadeesh



6 A novel Prins-

alkynylation reaction for the synthesis of 4-phenacyl tetrahydropyrans

J. S. Yadav, B. V. Subba Reddy, Y. J. Reddy, Bh. P. Reddy, P. A. Reddy


5 Silylalkyne-Prins

cyclization: a novel synthesis of 4-iododihydro pyrans

J. S. Yadav, N. Thrimurtulu, K. A. Lakshmi, A.R. Prasad, B.V. Subba Reddy


4 A novel aza-Prins-

Friedel–Crafts reaction for the synthesis of 4-arylpiperidines

J. S. Yadav, B. V. Subba Reddy, K. Ramesh, G.G.K.S.N.Kumar, R. Grée


3 Reductive etherification of carbonyl compounds using polymethylhydrosiloxane activated by molecular iodine

J. S. Yadav, B. V. Subba Reddy, K. S. Shankar, T. Swamy



A. Vinu, P. Kalita, H. Oveisi, M.A.Chari, R.Pal , B. V. Subba Reddy*


1 Zinc-mediated alkylation

and acylation of 1,3-dicarbonyl compounds

J. S. Yadav, B. V. Subba Reddy, A. K. Mishra


Total list of publications (Annexure 1V)

1

S. No. Title Authors Journal

628 Tandem Prins strategy for the synthesis of spiropyrrolidine and spiropiperidine derivatives

B. V. Subba Reddy, Y. Suresh, C. Ravikumar Reddy, M. Rajashekhar Reddy, B. Sridhar



B. V. Subba Reddy, M. Ramana Reddy, S.Gopal Reddy, B. Sridhar, and S. Kiran Kumar


626 A novel domino cyclization for the stereoselective synthesis of indeno[2,1-c]pyran and cyclopenta [c]pyran derivatives

B. V. Subba Reddy, N. Prudhviraju, B. Someswarao, B. J. M. Reddy, B. Sridhar, M. Kanakaraju, A. C. Kunwar



B. V. Subba Reddy, G. Karthik, T. Rajasekaran, B. Sridhar

Eur. J. Org. Chem. 2015, 2038.

624 Tandem Prins/Wagner/Ritter process for the stereoselective synthesis of oxabicyclo[4.2.0] octanyl amide and (tetrahydrofuran-3-yl) cyclobutyl)amide derivatives

B. V. Subba Reddy, K. Muralikrishna, N. Jagdeesh Babu, K. Sirisha, A. V. S. Sarma



B. V. Subba Reddy, A. Venkateswarlu, B. Sridevi, M. Kanakaraju, A. C. Kunwar, G. Gayathri

Org. Biomol. Chem., 2015, 13, 2669.

622 Sequential glycosylation/endo-dig cyclization of sugar enynones for the synthesis of pyrano[3,2-c]furan scaffolds

B. V. Subba Reddy, V. Veerabhadra Reddy, G. Karthik, B. Jagadeesh

Tetrahedron 2015, 71, DOI:10.1016/j.tet.2015.02.089

621 A short and highly convergent approach for the synthesis of rutaecarpine derivatives

B. V. Subba Reddy, R. Anji Babu, B. J. M. Reddy, B. Sridhar, T. R. Murthy, P. Pranathi, S. V. Kalivendi, T. P. Rao

RSC Advances 2015, 5, 27476.


2

620 BF3.OEt2-catalyzed synthesis of 1-(tetrahydropyran-3-yl)-1, 3-dihydroisobenzofuran and trans-fused hexahydro pyrano [3,2-c]chromene derivatives

B. V. Subba Reddy, Ch. Syama Sundar, M. Ramana Reddy, B. Sridhar, C. Suresh Reddy

Synthesis-Stuttgart 2015, 46, DOI: 10.1055/s-0034-1380177.


G. Niranjan Reddy, B. Maheshwar Rao, M. Vijay, B. L. A. Prabhavathi Devi, R. B. N. Prasad, B. V. Subba Reddy

Canadian J. Chem., 2015, 93, 341.


B. V. Subba Reddy, A.Venkateswarlu, B. Sridevi,

Salem S. Aldeyab, Ajayan VinuϮ

J. Nanosci. and Nanotech. 2015 DOI:10.1166/jnn.2015.10671.

617 Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds

B. V. Subba Reddy, S. Gopal Reddy, M. Ramana Reddy, Manika Pal Bhadra, A. V. S. Sarma

Org. Biomol. Chem., 2014, 15, 7257.

616 Stereoselective Synthesis of Hexahydro-1H-spiro[isoquinoline-4,4'-pyran] Scaffolds through an Intramolecular Prins Cascade Process

B. V. Subba Reddy, M.

Durgaprasad, B. Sridhar J. Org. Chem. 2015, 80,

653.

615


B. V. Subba Reddy, V. Swathi, Manisha Swain, Manika Pal Bhadra, B. Sridhar, D. Satyanarayana B. Jagadeesh



B. V. Subba Reddy, R. Anji Babu, M. R. Reddy, B. J. M. Reddy, B. Sridhar

RSC Advances, 2014, 4, 44629.


P. L. Reddy, M. Lakshmi Devi, S. Satyanarayana, Ashita Singh, T.V. Reddy, J. P.Sridevi, G. Raja Sekhar, P. Yogeeswari, D. Sriram, U. S. Murty, U. Ramesh, B. V. Subba Reddy, R. Narender

Eur J Med Chem. 2014, 84, 118.


3

612 Aminol initiated Prins cyclization for the synthesis of octahydro-1H-pyrano[3,4-c]pyridine and hexahydro-1H-furo[3,4-c]pyrroles

B. V. Subba Reddy, S. Gopal Reddy, M. Ramana Reddy, B. Sridhar, Manika Pal Bhadra


611 Highly regio- and diastereoselective three-component reaction of acyclic/cyclic donor-acceptor carbenoids for the synthesis of angularly fused furocoumarins and spiro oxindolylfurocoumarins

G. Karthik, T. Rajasekaran, B. Sridhar, B. V. Subba Reddy


610 Stereoselective total syntheses of solifenacin and N-acetyl-1-(4-chlorophenyl)-6,7-dimethoxytetrahydro isoquinoline

R. Anji Babu, N. Siva Senkar Reddy, B. Jagan Mohan Reddy, B. V. Subba Reddy



P. Padmaja, G. Koteswara Rao, A. Indrasena, B. V. Subba Reddy, N. Patel, A. Basha Shaik, P. N. Reddy, P. K. Dubey, M. P. Bhadra

Org. Biomol. Chem., 2014, 15, 1404.

608 A concise total synthesis of lyngbic acid, hermitamides A and B

S. Satyanarayana, B. V. Subba Reddy, R. Narender


607 Four component, one-pot synthesis of N-alkyl-4-oxo-3-phenylhexahydro-4H-spiro{[1,3]dioxolo[4',5':4,5] furo[2,3-f][1,2,3]triazolo [1,5-a][1,4]diazepine-9,1'-cyclohexane}-6-carboxamide derivatives

B. V. Subba Reddy, N. Majumder, T. Prabhakar Rao



4

606 Catalyst and solvent-free cyclopropanation of electron-deficient olefins with cyclic diazoamides for the synthesis of spiro[cyclopropane-1,3 '-indolin]-2 '-one derivatives

G. Karthik, T. Rajasekaran, B. Sridhar, B. V. Subba Reddy


605 Au(I)/Ag(I)-catalyzed annulation of sugar aldehyde tethered with 3-phenylprop-2-yn-1-yl ether with aryl amines for the pyrano[4,3-b]quinoline derivatives

B. V. Subba Reddy, N. Majumder, B. Sridhar


604 A New Stereoselective Total Synthesis of Phomonol

B. V. Subba Reddy, L. Srinivas, P. S. K. Reddy, B. P. Reddy, A. R. Prasad, J. S. Yadav


603 A Formal Synthesis of Herboxidiene/GEX1A

J. S. Yadav, G. M. Reddy, S. R. Anjum, B. V. Subba Reddy

Eur. J. Org. Chem. 2014, 4389.

602 InBr3-Catalyzed Stereoselective Synthesis of 3,4-Disubstituted Hexahydro-1H-furo[3,4-c]pyran Derivatives

B. V. Subba Reddy, M. R. Reddy, B. Sridhar, C. S. Reddy


601 A novel Prins reaction for the synthesis of hexahydro-8, 8-dimethyl-1H-isochromen-7-ol derivatives

B. V. Subba Reddy, S. R. Anjum, G. M.Reddy, B. Sridhar


600


B. V. Subba Reddy, S. M. Reddy, Manisha Swain

RSC Advances, 2014, 4, 9107.


B. V. Subba Reddy, R. N. Rao, B. Kumaraswamy, J. S. Yadav



5

598 Prins Spirocyclization for the Synthesis of Spiro[isobenzofuran-pyran] Derivatives

B. V. Subba Reddy, Harish Kumar, P. S. Reddy, S. K. Kumar

Eur. J. Org. Chem., 2014, 4234.


B. V. Subba Reddy, M. R. Reddy, B. Sridhar,S. K. Kumar

Org. Biomol. Chem., 2014, 12, 4754.

596 A green approach towards the synthesis of enantio pure diols using Horse Radish Peroxidas enzyme immobilized on magnetic nanoparticles

S. S. Deepthi, E. Prasad, B. V. Subba Reddy, B. Sreedhar, A. B. Rao

Green and Sustainable Chemistry, 2014, 4, 15.

595 Stereoselective synthesis of C19-C27 fragment of bryostatin 11

J S Yadav, T. Swamy, B. V. Subba Reddy, V. Ravinder


594 o-Benzenedisulfonimide as a recyclable homogeneous organocatalyst for an efficient and facile synthesis of 4-amidotetrahydropyran derivatives through Prins-Ritter reaction

B. V. Subba Reddy, Supriya Ghanty


593 B(C6F5)3-catalyzed Prins/Ritter reaction: a novel synthesis of hexahydro-1H-furo[3,4-c]pyranyl amides

B. V. Subba Reddy, Supriya Ghanty, Ch. Kishore


592 Recent Advancesin Dye Sensitized Solar Cells

U. Mehmood, S. Rahman, K. Harrabi, I. A. Hussein, B. V. Subba Reddy

Advances in Materials Science and Engineering 2014, 1.

591 Montmorillonite Clay Catalyzed Three Component, One-Pot Synthesis of 5-Hydroxyindole Derivatives

B. V. Subba Reddy, P. Sivaramakrishna Reddy, Y. Jayasudhan Reddy, N. Bhaskar, and B. Chandra Obula Reddy



6

590 Prins cascade cyclization for the synthesis of 1,9-dioxa-4-azaspiro[5.5]undecane derivatives

B. V. Subba Reddy, M.

Durgaprasad, B. Sridhar, S. K. Kumar



B. V. Subba Reddy, A.Venkateswarlu, P.Borkar, J. S. Yadav, B. Sridhar, René GréeϮ


588 Stereoselective synthesis of tetrahydropyran-tetrahydrofuran (THP-THF) core of (+)-muconin via Prins cyclization

J. S. Yadav, U. V. S. Reddy, B. V. Subba Reddy


587 InCl3-catalyzed Prins bicyclization for the synthesis of spirotetrahydropyrans

B. V. Subba Reddy, S. Jalal, S. K. Kumar

RSC Advances, 2014, 4. 16739.

586 Thee-component, one-pot synthesis of hexahydroazepino [3,4-b]indole and tetrahydro-1H-pyrido[3,4-b]indole derivatives and evaluation of their cytotoxicity

B. V. Subba Reddy, A. V. Ganesh, M. Vani, T. R. Murthy, S. V. Kalivendi, J. S. Yadav


585 Diastereoselective Synthesis of (+)-Pseudohygroline via Proline-catalyzed alpha-Hydroxylation

B. Anusha, U.V. S. Reddy, B.V. Subba Reddy, C. S.Reddy

Natural Product Communications, 2014, 9, 633.


B. V. Subba Reddy, Manisha Swain, S. M. Reddy, J. S. Yadav, B. Sridhar

Eur. J. Org. Chem., 2014, 3313.


Z. Begum, Ch.Kishore, V. Veerabhadra Reddy, B. V. Subba Reddy



7

582 GaCl3-catalyzed activation of alkynyl glycosides for the synthesis of O-glycosides

J. S. Yadav, N. N. Yadav, M. K. Gupta, N. Srivastava, B. V. Subba Reddy


581 Biogenic preparation of gold nanostructures reduced from Piper longum leaf broth and their electrochemical studies

K. Mallikarjuna, G. Narasimha, N. J. Sushma, G. R. Dillip, B. V. Subba Reddy, B. Sreedhar, B. D. P. Raju


580 Stereoselective total synthesis of 11-methoxycurvularin

J. S. Yadav, Ch. D. Vani, N. Bhasker, B. V. Subba Reddy

Arkivoc, 2014, 291.

579 Stereoselective synthesis of oxylipins, (8R,9R,10S)-trihydroxyoctadeca-6Z-enoic acid and (6S,9R,10S)-trihydroxyoctadeca-7E-enoic acid

J. S.Yadav, K. S. Shankar, B. V. Subba Reddy


578 Stereoselective total synthesis of decarestrictine I

J. S. Yadav, M. Venkatesh, A. S. Kumar, P. A. N. Reddy, B. V. Subba Reddy, A. R. Prasad


577 Stereoselective total synthesis of 4-((3S,5R)-3,5-dihydroxy nonadecyl)phenol

J. S. Yadav, P. A.N. Reddy, A. S. Kumar, A. R. Prasad, B. V. Subba Reddy


576 Stereoselective Synthesis of 2-(2-hydroxyalkyl)piperidine alkaloids through Prins/Ritter reaction

B.V. Subba Reddy, S. Ghanty, N. S. S. Reddy, Y. J. Reddy, J. S. Yadav


575

574

Ugi three-component coupling reaction for the synthesis of 2-(6-oxo-11-phenyl-7,8-dihydrobenzo[b]pyrrolo [1,2-d][1,4]diazocin-5(6H)-yl)-2-phenylacetamide derivatives

Asymmetric Michael/ hemiketalization of 5-hydroxy-2-methyl-4H-pyran-4-one to beta,gamma-unsaturated alpha-ketoesters catalyzed by a bifunctional rosin-indane amine thiourea catalyst

P. L. Reddy, D. A. Kumar, M. L. Devi, T. V. Reddy , R. Narender, B. V. Subba Reddy

B. V. Subba Reddy, Manisha Swain, S. Madhusudana Reddy, J. S. Yadav, B. Sridhar


RSC Advances, 2014, 4. 42299.


8

573 A convergent and stereoselective total synthesis of phomolides G, H

B. V. Subba Reddy, P. S. Reddy, B. P. Reddy, J. S. Yadav

Synlett, 2014, 501.

572 First example of quinine-squaramide catalyzed enantioselective addition of diphenyl phosphite to ketimines derived from isatins

J. George, B. Sridhar, B. V. Subba Reddy

Org. Biomol. Chem., 2014, 12, 1595.

571 Highly Diastereoselective Reaction of alpha-Diazoesters with Aryl Alcohols and Isatin Imines: Rapid Access to Oxindole-Derived alpha-Alkoxy-beta-amino Acid Derivatives with Two Adjacent Quaternary Carbon Centers

T. Rajasekaran, G. Karthik, B. Sridhar, S. K. Kumar, B. V. Subba Reddy

Eur. Journal of Organic Chemistry, 2014, 2221.


Ch. Srilakshmi, A. B. Rao, M. Laxminarsu, B. V. Subba Reddy



B. V. Subba Reddy, R. N. Rao, N.S.Reddy, R. Somaiah, J. S. Yadav, Ravi Subramanyam



B. V. Subba Reddy, V. V. Reddy, K. Praneeth


567 Stereoselective total synthesis of penaresidin A starting from D-galactal

B. V. Subba Reddy, Ch. Kishore, A. S. Reddy


566 The stereoselective total synthesis of almorexant

N. S. S. Reddy, B. V. Subba Reddy



A. S. Reddy, Ch. Kishore, B. V. Subba Reddy



9

564 Stereoselective total synthesis of PF 1163A

Harish Kumar, A. Srinivas Reddy, B. V. Subba Reddy


563 Green Synthesis of Curcumin Capped Gold Nanoparticles and Evaluation of Their Cytotoxicity

Ch. Sreelakshmi1, Nidhi Goel, K. K. R. Datta, A.Anthony, U. Ramesh, B. V. Subba Reddy


562 Heteropoly acid catalyzed synthesis of 8-methyl-2-aryl/alkyl-3-oxabicyclo [3.3.1]non-7-ene derivatives through (3,5)-oxonium-ene reaction

R. Anjibabu, S. Samaresh, B. J. M. Reddy, B. Rajkumar, B. V. Subba Reddy



B. V. Subba Reddy, A. Venkateswarlu, G. Niranjan Reddy



B. V. Subba Reddy, B. P. Reddy, N. Swapnil, J. S.Yadav


559 Montmorillonite Clay catalyzed three component, one-pot synthesis of 5-hydroxyindole derivatives

B. V. Subba Reddy, P. S. Reddy, Y. J. Reddy

Bulletin of the Korean Chemical Society, 2013, 34, 2968.

558 Stereoselective total synthesis of xyolide

B. V. Subba Reddy, P. S. Reddy, B. P. Reddy


557 Stereoselective total synthesis of (-)-brevisamide

J. S. Yadav, N. M. Reddy, Md. A. Rahman, B. V. Subba Reddy

Tetrahedron, 2013, 69, 8618.

556 Divergent enantioselective total synthesis of siphonarienal, siphonarienone, and pectinatone

J. S. Yadav, D. N. Chary, N. N. Yadav, B. V. Subba Reddy



10

555 A Concise and Convergent Total Synthesis of Two Novel Cytotoxic Hydroquinones, Lanneaquinol and (R)-2 '-Hydroxylanneaquinol

B. V. Subba Reddy, B. Anusha, U. V. S. Reddy


554 A short and facile stereoselective total synthesis of cryptocarya diacetate

J. S. Yadav, P. M. K. Reddy, K. M. Gupta, B. V. Subba Reddy



B. V. Subba Reddy, P. J. Reddy, C. Suresh



S. Satyanarayana, K. P. Kumar, P. L. Reddy, R. Narender, G. Narasimhulu, B. V. Subba Reddy



S. Satyanarayana, K. P. Kumar, P. L. Reddy, R. Narender, G. Narasimhulu, B. V. Subba Reddy


550 Stereoselective total synthesis of (+)-8-ethylnorlobelol from anti-1,3-aminoalcohols

B. V. Subba Reddy, B. P. Reddy, P. S. Reddy, Y. J. Reddy, J. S. Yadav


549 Stereoselective synthesis of hexahydro-1H-pyrano/thiopyrano [3,4-c]quinoline derivatives through a Prins cascade cyclization


Journal of Organic Chemistry, 2013, 78, 8161.

548 A convergent and stereoselective total synthesis of (-)-crispine A, (-)-benzo[a]quinolizidine and (-)-salsolidine

N. S. S. Reddy, B. J. M. Reddy, B. V. Subba Reddy


547 An expeditious synthesis of 2,3,6-trisubstituted tetrahydropyrans through (3,5)-oxonium-ene cyclization by molecular iodine

N. P. Raju, B. J. M. Reddy, R. Anjibabu, B.V. Subba Reddy



11

546 Dual behavior of isatin-based cyclic ketimines with dicarbomethoxy carbene: expedient synthesis of highly functionalizedspirooxindolyl oxazolidines and pyrrolines

T. Rajasekaran, G. Karthik, B. Sridhar, B. V. Subba Reddy


545 Enantioselective addition of 2-hydroxy-1,4-naphthoquinone and 1,3-dicarbonyls to β-nitroalkenes catalyzed by a novel bifunctional rosin-indane amine thiourea catalyst

B. V. Subba Reddy, Manisha Swain, S. M. Reddy

RSC Advances, 2013, 3, 8756.


B. M. Rao, G. N. Reddy, T. V. Reddy, B. L. A. P. Devi, R. B. N. Prasad, J. S. Yadav, B. V. Subba Reddy


543 Stereoselective synthesis of anti-1,3-aminoalcohols via reductive opening of 4-amido tetrahydropyrans derived from the Prins/Ritter sequence

J. S. Yadav, Y. J. Reddy, P. A. N. Reddy, B. V. Subba Reddy


542 Cu(OTf)2-catalyzed synthesis of 2,3-disubstituted indoles and 2,4,5-trisubstituted pyrroles from α-diazoketones

B. V. Subba Reddy, M. R. Reddy, Y. G. Rao, J. S. Yadav, B.Sridhar



A. S. Kumar, K. K. R. Datta, T. S. Rao, K. V. Raghavan, M. Eswaramoorthy, B. V. Subba Reddy


540 Iron(III)-catalyzed highly efficient, one-pot synthesis of triazolo[1,2-a]indazoletriones and spiro-triazolo[1,2-a]indazoletetraones

B. V. Subba Reddy, N. Umadevi, G. Narasimhulu, J. S. Yadav


539 Enantioselective Mukaiyama Michael reaction of silyl enol ethers to 2-enoylpyridine N-oxides catalyzed by copper- bis(oxazoline) complex




12

538 Prins cascade cyclization reaction for the synthesis of angularly-fused tetrahydropyran and piperidine derivatives

B. V. Subba Reddy, Harish Kumar, P.Borkar, J. S. Yadav, B. Sridhar

Eur. J. Org. Chemistry 2013, 1993.


B. V. Subba Reddy, S. Jalal, P. Borkar, J.S. Yadav, P. G. Reddy, A.V.S. Sarma


536 SN2 substitution reaction of 2-C-acetoxymethyl glycals catalyzed by iodine: a novel synthesis of 2-C-N-arylamidomethyl glycals

J. S. Yadav, G. Narasimhulu, N. Umadevi, Y. V. Reddy, B. V. Subba Reddy



M. Raghu, M. Rajasekhar, B. C. O. Reddy, Ch S.Reddy, B. V. Subba Reddy



Harish Kumar, A. Srinivas Reddy, J. S.Yadav, B. V. Subba Reddy

Synlett, 2013, 1415.


B. V. Subba Reddy, A. Venkateswarlu, B. Prashant, J. S. Yadav


532 A formal stereoselective synthesis of (-)-brevisamide

J. S. Yadav, A. Raju, K. Ravindar, B. V. S. Reddy


531 A novel Prins bicyclization strategy for the synthesis of sugar annulated furopyran scaffolds

S. Nikhil, P. P. Reddy, B. Sridhar, B. V. Subba Reddy

Synlett, 2013, 1263.

530 Solvent-free cyanoethylation of selected alcohols using Amberlyst A-21 polymer resin

M. Trinadh, T. Rajasekhar, B. Bhadru, J. Gopinath, V. Santosh, B. V. Subba Reddy, A.V.S. Sainath

J. Appl. Polym. Sci. 2013, 128, 795.


13

529 Novel protocol for the synthesis of octahydropyrano- and thiopyrano [4,3-a]carbazole derivatives via Prins/Friedel–Crafts cyclization

B. V. Subba Reddy, P. S. Reddy, J. S. Yadav, B. Sridhar


528 Sugar thiourea catalyzed highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone to β-nitroalkenes

B. V. Subba Reddy, S. M. Reddy, Manisha Swain


527 Copper salt of 12-tungstophosphoric acid: an efficient and reusable heteropoly acid for the Click Chemistry

K. V. Purnima, D. Sreenu, N. Bhasker, K. Nagaiah, N. Lingaiah, B. V. Subba Reddy, J. S. Yadav

Chinese. J. Chem. 2013, 31, 534.

526 Bismuth(III) Salts as synthetic tools in organic transforma-tions

J. S. Yadav, A. Antony, B. V. Subba Reddy


525 Gold-Catalyzed domino cycloisomerization/Pictet–Spengler reaction of 2-(4-aminobut-1-yn-1-yl)anilines with aldehydes: synthesis of tetrahydropyrido[4,3-b]indole scaffolds

B. V. Subba Reddy, Manisha Swain, S. M. Reddy, J. S. Yadav , B. Sridhar



N. S. S. Reddy, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy


523 The stereoselective total synthesis of (3R,5R)-sonnerlactone and (3R,5S)-sonnerlactone

J. S. Yadav, K. S. Shankar, A. S. Reddy, B. V. Subba Reddy


522 Synthetic studies toward potent cytostatic macrolide bryostatin: an expedient synthesis of C1–C10 fragment

J.S. Yadav, S. Aravind, G. M. Kumar, B. V. Subba Reddy


521 The first stereoselective total synthesis of the Z-isomer of cytospolide E

J.S. Yadav, T. Pandurangam, A. S. Kumar, P.A.N.Reddy, A.R. Prasad, B. V. Subba Reddy, K. R. Prasad, A.C. Kunwar



14


B. V. Subba Reddy, N. Umadevi, G. Narasimulu, J. S. Yadav


519 A novel strategy for the chiral 2,4,5-triol moiety and itsapplication to the synthesis of seimatopolide A and (2S,3R,5S)-(−)-2,3-dihydroxy- tetradecan-5- olide

B. P. Reddy, T. Pandurangam, J. S. Yadav, B. V. Subba Reddy


518 Studies directed towards the synthesis of bryostatin: a stereoselective synthesis of the C7-C16 fragment

J. S. Yadav, S. Aravind, G. M. Kumar, B. V. Subba Reddy



S. Chauhan, G. P. Mane, C. Anand, D. S. Dhawale, B. V. Subba Reddy, S. M. J. Zaidi, S. S. Al-Deyab, V. V. B. Subramanian, T. Mori, A. VinuϮ

Synlett 2012, 2237.

516 Total synthesis of 7-desmethoxyfusarentin and its methyl ether

P. J. Reddy, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy


515 First stereoselective total synthesis of decytospolides A and B

P. J. Reddy, A. S. Reddy, J.S. Yadav, B. V. Subba Reddy


514 A novel intramolecular Ugi 3CC for the synthesis of N-alkyl-3-oxo-2-aryl-1,2,3,4-tetrahydropyrazino [1,2-a]indole-1-carboxamides

B. V. Subba Reddy, S. K. Dey, J. S. Yadav, B. Sridhar



B. V. Subba Reddy, G. Narasimhulu, Y. V. Reddy, P.P. Chakravarthy, J. S. Yadav, B. Sridhar



15

512 In(OTf)3-catalyzed tandem aza-Piancatelli rearrangement/ Michael reaction for the synthesis of 3,4-dihydro-2H-benzo[b][1,4]thiazine & oxazines

B. V. Subba Reddy, Y. V. Reddy, P. S. Lakshumma , G. Narasimhulu, J. S. Yadav , B. Sridhar, P. P. Reddy, A. C. Kunwar

RSC Advances, 2012, 2, 10661.

511 Unprecedented synergistic effects between weak Lewis and Brønsted acids in Prins cyclization

P. Borkar, P.van de Weghe,Ϯ B. V. Subba Reddy, J. S. Yadav, René GréeϮ

Chem. Commun. 2012, 48, 9316.


B. V. Subba Reddy, S.Jalal, P. Borkar, J. S. Yadav, P. P. Reddy, A. C. Kunwar and B. Sridhar

Org. Biomol. Chem., 2012, 10, 6562.



Org. Biomol. Chem., 2012, 10, 4731.

508 An oxidative Prins & Prins/Friedel-Craftscyclization for the stereoselective synthesis of dioxabicycles & hexahydro-1H-benzo[f] isochromenes via the benzylic C-H activation

B. V. Subba Reddy, P. Borkar, J. S. Yadav, P. P. Reddy, A. C. Kunwar, B. Sridhar, René GréeϮ

Org. Biomol. Chem. 2012, 10, 1349.


B. V. Subba Reddy, M. Sreelatha, Ch. Kishore, P. Borkar, J. S. Yadav


506 A concise total syntheses of (-) -deoxocassine and (-)-deoxoprosophylline from D-xylose

Ch. Kishore, A. S. Reddy, J. S. Yadav, B. V. Subba Reddy


505


B. V. Subba Reddy, B. Divya, Manisha Swain, J. S. Yadav

Bioorg. Med.Chem. Lett. 2012, 22, 1995.


16

504 A novel tandem ene/Prins cyclization for the synthesis of octahydropyrano[2,3-c]pyrrole derivatives

B. V. Subba Reddy, S. R. Anjum, G. M., J. S. Yadav



K. P. Kumar, S. Satyanarayana,

P. L. Reddy, G. Narasimhulu, R.Narender, B. V. Subba Reddy


502 Chemoenzymatic approach for the total synthesis of (+)-bourgeanic acid

J. S. Yadav, T. S. Rao, N. N. Yadav, K. V. R.Rao, B. V. Subba Reddy, A. K. Ghamdi


501 Total synthesis of (-)-pyrenophorol

J. S. Yadav, G. M. Reddy, T. S. Rao, B. V. Subba Reddy, A. K. Ghamdi


500 Stereoselective synthesis of (4S,6S)-6-hydroxy-4-undeca-nolide: A Pheromone of the Giant White Butterfly Idea Leuconoe

J. S. Yadav, P.A.N. Reddy, Hissana Ather, A. S. Kumar, A. R. Prasad, B. V. Subba Reddy



B. V. Subba Reddy, D. N. Chaya, J. S.Yadav, René GréeϮ


498 Stereoselective total synthesis of putaminoxin


Synthesis 2012, 585

497 Gallium(III)-catalyzed cycloisomerization/Friedel-Crafts alkylation: a facile synthesis of 2,5-disubstituted furans

B. V. Subba Reddy, B. Bramha Reddy, K. V. R. Rao, J. S. Yadav


496 Pd-Aminoclay Nanocomposite as an Efficient Recyclable Catalyst for Hydrogenation and Suzuki Cross Coupling

A. S. Kumar, K. K. R. Datta, T. S. Rao, K. V. Raghavan, M. Eswaramoorthy, B. V. Subba Reddy



17

495


B. V. Subba Reddy, T. Rajasekaran, G. Karthik, T. P. Rao


494 A novel sugar based intramolecular Ugi 3CC for the N-alkyl-3-oxo-4-aryl-octahydrofuro[2,3-f][1,4] oxazepine-5-carboxamides

B. V. Subba Reddy, N. Majumder, T. P. Rao, B. Sridhar


493 Phosphomolybdic acid: a highly efficient solid acid for the synthesis of trans-4,5-disubstituted cyclopentenones

B. V. Subba Reddy, G.Narasimhulu, P.S. Lakshumma, Y. V. Reddy, J. S. Yadav


492 Honey Mediated Green Synthesis of Pd Nanoparticles for Suzuki Coupling and Hydrogenation of Conjugated Olefins

S. M. Reddy, K. K. R. Datta, Ch. Sreelakshmi, M. Eswaramoorthy, B. V. Subba Reddy


491 An efficient synthesis of 2-aryl-1,4-diketones via hydroacylation of enones

P. L. Reddy, K. P. Kumar, S. Satyanarayana, R. Narender, B. V. Subba Reddy


490 Rh2(OAc)4 catalyzed substrate selective [4+2]/[2+2] cycloaddition of acylketenes: a highly chemo- and regioselective synthesis of spiro (oxindolyl)oxazinones and β-lactams

B. V. Subba Reddy, G. Karthik, T. Rajasekaran, A. Antony, B. Sridhar


489 Quinazolinone-directed C-H activation: a novel strategy for the acetoxylation /methoxylation of arenes

B. V. Subba Reddy, G. Narasimhulu, N. Umadevi, J. S. Yadav

Synlett 2012, 1364


B. V. Subba Reddy, N. N. Yadav, N. Srivastava, J. S. Yadav, B.Sridhar



18

487 Iodine-catalyzed condensation of isatin with indoles: a facile synthesis of di(indolyl)indolin-2-ones and evaluation of their cytotoxicity

B. V. Subba Reddy, N. Rajeswari, M. Sarangapani, Y. Prashanthi, J. S. Yadav, G. R. Jones, A. Anthony


486 Recent Advances in the Applications of Ionic Liquids for the Synthesis of Bioactive Six-Membered N-Heterocycles

J. S. Yadav, A. Antony, B. V. Subba Reddy


485 BF3.OEt2-Catalyzed Unusual Formation of cis-2,3-Disubstituted Tetrahydrofuran Scaffolds

B. V. Subba Reddy, S. R. Anjum, G. M. Reddy, J. S. Yadav

Synlett, 2011, 2951.

484 Tandem Prins/Friedel-Crafts Cyclization for Stereoselective Synthesis of Heterotricyclic Systems

B. V. Subba Reddy, Prashant Borkar, J. S. Yadav, B. Sridhar,

René GréeϮ


483 Regioselective ortho-acetoxylation/methoxylation of N-(2-benzoylphenyl) benzamides via substrate directed C-H activation

B. V. Subba Reddy, G. Revathi, A. Srinivas Reddy, J. S. Yadav


482 InBr3-catalyzed three-component, one-pot synthesis of imidazo[1,2-a]pyridines

B. V. Subba Reddy, P. Sivaramakrishna Reddy, Y. Jayasudhan Reddy, J. S. Yadav


481 Stereoselective total synthesis of (+)-18-(6S,9R,10R)-bovidic acid

J. S. Yadav, K. Ramesh, U. V. Subba Reddy, B. V. Subba Reddy, A. K. Ghamdi


480 First stereoselective total synthesis and biological evaluation of Amphidinin B and its analogues

J. S. Yadav, A. Srinivas Reddy, Ch. Suresh Reddy, B. V. Subba Reddy, S. Venkateshwarlu, A. Anthony

European Journal of Organic Chemistry 2011, 696.


19


B. V. Subba Reddy, A. V. Ganesh, A. Siva Krishna, G. G. K. S. Narayana Kumar, J. S. Yadav


478 Total synthesis of cryptophycin-24 (arenastatin A) via Prins cyclization

J. S. Yadav, K.V. Purnima, B. V. Subba Reddy, K. Nagaiah, A.K. Ghamdi


477 Iodine-catalyzed conjugate addition of indoles onto en-1,4-dione: A novel synthesis of 3-(1-(1H-indol-3-yl)-2-oxo-2-phenylethyl)indolin-2-ones as antibacterial and antifungal agents

B. V. Subba Reddy, N. Rajeswari, M. Sarangapani, G. R. Reddy, Ch. Madan, K. P. Kumar, M. S. Rao



B. V. Subba Reddy, Ruchi Jain, K. Bhargavi, Manisha Swain, J. S. Yadav


475 Indium(III) Chloride Catalyzed, Novel and Efficient Synthesis of Sugar Annulated N-Aryltetrahydropyridines

B. V. Subba Reddy, Ch. D. Vani, Z. Begum, J. S. Yadav, T. P. Rao


474 Recent progress in transition metal catalysed hydrofunctionalisation of less activated olefins

J. S. Yadav, A. Antony, T. S. Rao, B. V. Subba Reddy


473 Green Synthesis Of Silver Nanoparticles Using Ocimum Leaf Extract And Their Characterization

K.Mallikarjuna, G. Narasimha, G. R. Dillip, B. Praveen, B. Sreedhar, C. Sreelakshmi, B. V. Subba Reddy, B. D. Prasad Raju

Digest J. Nanomaterials and Biostructures, 2011, 6, 181.

472 Total synthesis of (+)-Bourgeanic acid utilizing Desymmetrization strategy

J. S. Yadav, K. V. R.Rao, K. Ravindar, B. V. Subba Reddy


471 Quinoxaline-Directed C-H activation: A novel method for acetoxylation of arenes

B. V. Subba Reddy, K. Ramesh, J. S. Yadav

Synlett 2011, 169.


20

470 Triflic acid-promoted aza-Prins-Ritter reaction sequence: a novel synthesis of 4-amidopiperidine derivatives

B. V. Subba Reddy, K. Ramesh, A.V. Ganesh, G.G.K.S. N. Kumar, J.S. Yadav, René GréeϮ


469 Iodine-catalyzed formation of aza-dienes: a novel synthesis of angularly fused hexahydropyrano- and furo[3,2-c]quinoline derivatives

B. V. Subba Reddy, Harish Grewal



B. V. Subba Reddy, S. M. Reddy, Swain Manisha, Ch. Madan


467 Nano Fe3O4 as magnetically recyclable catalyst for the synthesis of α-aminophos phonates in solvent-free

B. V. Subba Reddy , A. Siva Krishna, A.V. Ganesh, G.G.K.S. Narayana Kumar


466 NBS or DEAD as effective reagents in α-thiocyanation of enolizable ketones with ammonium thiocyanate

B. V. Subba Reddy, S. Madhu Sudana Reddy, Ch. Madan


465 Cellulose-SO3H: an efficient and biodegradable solid acid for the synthesis of quinazolin-4(1H)-ones

B. V. Subba Reddy, A. Venkateswarlu, Ch. Madan, A. VinuϮ


464 A novel trifunctional organo-catalyst for the asymmetric aldol reaction: a facile enantioselective synthesis of β-hydroxy ketones

B. V. Subba Reddy, K. Bhavani, A. Raju, J. S. Yadav


463 Stereoselective total synthesis of (-)-cleistenolide

B. V. Subba Reddy, B. Phaneendra Reddy, T. Pandurangam, J. S. Yadav



21

462 Indium/Cu(II)-mediated one-pot synthesis of unsymmetri-cal diaryl amines from aryl boronic acids and azides

B. V. Subba Reddy, N. Sivasankar Reddy, Y. Jayasudhan Reddy, Y. Vikram Reddy



B. V. Subba Reddy, K. Praneeth, J. S. Yadav


460 BF3·OEt2-catalyzed tandem Prins Friedel–Crafts reaction: a novel synthesis of sugar fused diaryl hexahydro-2H-furo[3,2-b]pyrans

B. V. Subba Reddy, Dudhmal N. Chaya, J. S. Yadav, Deepak Chatterjee, A. C. Kunwar



B. V. Subba Reddy, Jimil George


458 Sodium borohydride / methoxydiethylborane mediated syn-1,3-stereoselective total synthesis of Herbarumin-III

J S Yadav, G. Narasimhulu, Y. V. Reddy, B. V. Subba Reddy

Indian Journal of Chemistry, Section B: Organic Chemistry, 2011, 50, 1075.

457 Enantioselective Total Synthesis of (+)-Vittatalactone

J. S. Yadav, N. N. Yadav, T S Rao, B. V. Subba Reddy, A. A Ghamdi


456 Honey Derivatized Au and Ag Nanoparticles and Evaluation of Its Antimicrobial Activity

Sreelakshmi, Ch.; Datta K. K. R.; Yadav J. S; B. V. Subba Reddy


455 Palladium(II)-Catalyzed Auxiliary-Directed C-H Activation for the Regioselective ortho-Arylation of N-(2-Benzoylphenyl) benzamides

B. V. Subba Reddy, G. Revathi, A. S. Reddy, J. S. Yadav

Synlett, 2011, 2374.

454 Concise Total Synthesis of (-)-cis-Aerangis Lactone and (-)-cis-Cognac Lactone

J. S. Yadav, R. N. Rao, B. P. Kumar, R. Somaiah, B. V. Subba Reddy



22

453 A practical synthesis of bis(indolyl)methanes employing boric acid

J. S. Yadav, M. K. Gupta, Ruchi Jain, N. N. Yadav, B. V. Subba Reddy


452 Stereoselective Total Synthesis of Leiocarpin C and (+)-Goniodiol

J. S. Yadav, V. Hari Krishna, A. Srilatha, R. Somaiah, B. V. Subba Reddy


451 Multi-Component Reactions Using Indium(III) Salts

J. S. Yadav, Aneesh Antony, Jimil George, B. V. Subba Reddy


450 Recent Developments in Indium Metal and Its Salts in Organic Synthesis

J. S. Yadav, Aneesh Antony, Jimil George, B. V. Subba Reddy


449 Gold Nanoparticles Embedded in a Mesoporous Carbon Nitride Stabilizer for Highly Efficient Three-Component Coupling Reaction

K. K. R. Datta, B. V. Subba Reddy, K. Ariga, Ajayan VinuϮ

Angew. Chem. Int. Engl. Ed., 2010, 49, 5961.

448 Samarium Triflate as Mild and Efficient Catalyst for Aza-Diels-Alder Reaction: A Facile Synthesis of cis-Fused Pyrano- and Furanoquinolines

A. Venkat Narsaiah, A. Ramesh Reddy, B. V. Subba Reddy, J. S. Yadav


447 HBF4·OEt2 as a mild and versatile reagent for the Ritter amidation of olefins: a facile synthesis of secondary amides

B. V. Subba Reddy, N. Sivasankar Reddy, Ch. Madan, J.S. Yadav



M. A. Chari, D. Shobha, El-Refaie Kenawy, S. S. Al-Deyab, B. V. Subba Reddy, Ajayan VinuϮ


445 Efficient Synthesis of 2,3,4-Trisubstituted Quinolines via Friedländer Annulation with Nanoporous Cage-Type Aluminosilicate AlKIT-5 Catalyst

S. Chauhan, R. Chakravarti, S. M. J. Zaidi, S. S. Al-Deyab, B. V. Subba Reddy, Ajayan VinuϮ

Synlett, 2010, 2597.


23

444 Ugi-type four-component reaction for a novel synthesis of 5-oxo-perhydrofuro[3,2-b]pyran carboxylate derivatives

B. V. Subba Reddy , N. Majumder, A.V. H.Gopal, D. Chatterjee, A.C. Kunwar



B. V. Subba Reddy, A. Venkateswarlu, G.G.K.S. N. Kumar, A. VinuϮ


442 Indium(III) chloride catalyzed three-component coupling reaction: A novel synthesis of 2-substituted aryl(indolyl)kojic acid derivatives as potent antifungal and antibacterial agents

B. V. Subba Reddy, M. R. Reddy, Ch. Madan, K. P. Kumar, M. S. Rao


441 A practical total synthesis of (+)-Spirolaxine methyl ether

J. S. Yadav, M. Sreenivas, A. S. Reddy, B. V. Subba Reddy


440 Total synthesis of Rhoiptelol B

J. S. Yadav, T. Pandurangam, V. V. B. Reddy, B. V. Subba Reddy


439 Highly Efficient Friedel-Crafts Alkylation of Indoles and Pyrrole Catalyzed by Mesoporous 3D Aluminosilicate Catalyst with Electron-Deficient Olefins

T. S. Naidu, V. V. B. Subramanian, M. A. Chari, T. Mori, S. M. J. Zaidi, S. S. Al-Deyab, B. V. Subba Reddy, A. VinuϮ

Synlett, 2010, 2813.

438 Stereoselective Total Synthesis of (3R,5R)-5-Hydroxy-de-O-methyllasiodiplodin via the Prins Cyclization

J. S. Yadav, N. Thrimurtulu, Md. Ataur Rahman, J. S. Reddy, A. R. Prasad, B. V. Subba Reddy


437 InCl3-catalyzed three-component reaction: a novel synthesis of dihydropyrano [3,2-b]chromenediones under solvent-free conditions

B. V. Subba Reddy, M. R. Reddy, G. Narasimhulu, J. S. Yadav



24

436 Stereoselective total synthesis of (+)-garvensintriol

J.S. Yadav, U.V. S. Reddy, B. Anusha, B. V. Subba Reddy


435 Iodine/Et3SiH: a novel reagent system for the synthesis of 3-aryl-1H-indenes from 1,3-diaryl propargyl alcohols

B. V. Subba Reddy, B. B. Reddy, K. V. R. Rao, J. S. Yadav



B. V. Subba Reddy, A. M. Reddy, D.Somashekar, J. S. Yadav, B. Sridhar


433 Polyethyleneglycol-400 as a Reusable Solvent for 1,4-Dipolar Cycloadditions via Three-Component Reaction

B. V. Subba Reddy, D. Somashekar, A. M. Reddy, J. S. Yadav, B. Sridhar



B. V. Subba Reddy, Ch. D. Vani, J. S. Yadav


431 Pd(OAc)2-catalyzed C-H activation of indoles: a facile synthesis of 3-cyanoindoles

B. V. Subba Reddy, Z. Begum, Y. J. Reddy, J. S. Yadav


430 Sc(OTf)3-catalyzed intramolecular aza-Prins- cyclisation for the synthesis of heterobicycles

B. V. Subba Reddy, P. Borkar,

P. P. Chakravarthy, J. S. Yadav, René GréeϮ


429 Novel intramolecular aza-Diels-Alder reaction: a facile synthesis of trans-fused 5H-chromeno[2,3-c]acridine derivatives

B. V. Subba Reddy, Aneesh Antony, J.S. Yadav


428 Iodine as a versatile catalyst for the hydroalkylation of vinyl arenes with 1,3-diketones

J.S. Yadav, B. V. Subba Reddy, T. S. Rao, K. Bhavani, A. Raju



25

427 HBF4.OEt2 as a versatile reagent for the Hosomi-Sakurai allylation and Prins cyclisation: one-pot synthesis of symmetrical 4-fluoro tetrahydropyrans

J. S. Yadav, B. V. Subba Reddy, B. Anusha, U. V. S. Reddy, V. V. B. Reddy.


426 Substrate-controlled stereoselective synthesis of Ophiocerin C

J. S. Yadav, N. R. Reddy, B. B. M. Krishna, Ch. V. Vardhan, B. V. Subba Reddy


425 Total synthesis of Aculeatins A and B from L-malic acid

J. S. Yadav, Y. Gopala Rao, D. Chandrakanth, K. Ravindar, B. V. Subba Reddy


424 Versatile intramolecular aza-Prins and Prins cyclization of aryl epoxides: a novel synthesis of diaza-,oxa-aza- and dioxa-bicycles

J.S.Yadav, P. Borkar, P. P. Chakravarthy, B. V. Subba Reddy, A. V. S. Sarma, B. Sridhar, René GréeϮ


423 Stereoselective total synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one via Prins cyclisation

J. S. Yadav, D. Chandrakanth , Y. G. Rao, K. Ravindar, B. V. Subba Reddy


422 Sc(OTf)3-catalysed one-pot Ene-Prins cyclization: a novel synthesis of octahydro-2H-chromen-4-ols

J. S. Yadav, B. V. Subba Reddy, A. V. Ganesh, G. G. K. S. N. Kumar


421 Allylic nucleophilic substitution of Morita-Baylis-Hillman acetates with isocyanides: a facile synthesis of trisubstituted olefins

J. S.Yadav, B. V. Subba Reddy, A. P. Singh, N. Majumdar


420 Domino Knoevenagel-hetero-Diels-Alder reactions: a stereoselective synthesis of sugar annulated furo[3,2-b]pyrano[4,3-d]pyrans

J. S. Yadav, B. V. Subba Reddy, A.V. H. Gopal, R. N. Rao, R. Somaiah, P. P. Reddy, A. C. Kunwar



26

419 Total synthesis of (+)-pseudohygroline

J. S. Yadav, G. Narasimhulu, N. M. Reddy, B. V. Subba Reddy


418 Stereoselective total synthesis of 11-α-methoxy curvularin and 11-β-methoxy curvularin



417 Stereoselective Synthesis of (10S,12S)-10-hydroxy-12-methyl-1-oxacyclododecane-2,5-dione via Prins cyclisation

J. S. Yadav, N. Thrimurtulu, M. Venkatesh, K. V. R. Rao, A. R., Prasad, B. V. Subba Reddy


416 An expeditious synthesis of 4-fluoropiperidines via aza-Prins cyclization

J. S. Yadav, B. V. Subba Reddy, K. Ramesh, G. G. K. S. N. Kumar, René GréeϮ


415 Total synthesis of (+)-Aculeatin D and (+)-6-epi-Aculeatin D

J. S. Yadav, K. V. R. Rao, K. Ravindar, B. V. Subba Reddy

Synlett, 2010, 51.

414 Stereoselective total synthesis of (–)-Ovalicin

J. S. Yadav, P. N. Reddy, B. V. Subba Reddy

Synlett, 2010, 457.

413 3CC reaction of d-hydroxy-a,b-unsaturated aldehyde, aryl amine and 1,3-diketone: a novel synthesis of oxa-aza bicycles

B. V. Subba Reddy, Ch. Divyavani, Z. Begum, J. S. Yadav


412 Stereoselective total synthesis of Goniothalesdiol A via Chiron approach

J. S. Yadav, R. N. Rao, R. Somaiah, V. Harikrishna, B. V. Subba Reddy

Helvetica Chimica Acta, 2010, 1362.

411 Stereoselective total synthesis of decarestrictine-J via Ring Closing Metathesis (RCM)

J. S. Yadav, K. A. Lakshmi, N. M. Reddy, A. R. Prasad, B. V. Subba Reddy


410 First example of carbohydrate based Prins cyclization: a novel class of sugar annulated tetrahydropyrans

J. S. Yadav, B. V. Subba Reddy, A. P. Singh, D. N.Chaya, D. Chatterjee, A. C. Kunwar


409 First example of FeCl3-catalyzed alkylation of indoles with pinenes

J. S. Yadav, B. V. Subba Reddy, G. Narasimhulu, N. S. Reddy, P. N. Reddy, K.V. Purnima, P. Naresh, B. Jagadeesh



27

408 A novel Prins-alkynylation reaction for the synthesis of 4-phenacyl tetrahydropyrans

J. S. Yadav, B. V. Subba Reddy, Y. J. Reddy, Bh. P. Reddy, P. A. Reddy


407 Silylalkyne-Prins cyclization: a novel synthesis of 4-iododihydro pyrans

J. S. Yadav, N. Thrimurtulu, K. A. Lakshmi, A.R. Prasad, B. V. Subba Reddy


406 A novel aza-Prins-Friedel–Crafts reaction for the synthesis of 4-arylpiperidines

J. S. Yadav, B. V. Subba Reddy, K. Ramesh, G.G.K.S.N.Kumar, R. GréeϮ


405 The reductive etherification of carbonyl compounds using polymethylhydrosiloxane activated by molecular iodine

J. S. Yadav, B. V. Subba Reddy, K. S. Shankar, T. Swamy



A. Vinu,Ϯ P. Kalita, H. Oveisi, M. A. Chari, R.Pal, B. V. Subba Reddy


403 Zinc-mediated alkylation and acylation of 1,3-dicarbonyl compounds

J. S. Yadav, B. V. Subba Reddy, A. K. Mishra


402 Highly diastereoselective allylation of lactols and their ethers using molecular iodine

J. S. Yadav, B. V. Subba Reddy, A. Srinivas Reddy, Ch. Suresh Reddy, S. Satyanarayana Raju


401 Bismuth(III)-catalyzed hydrolysis of epoxides and aziridines: an efficient synthesis of vic-diols and β-amino alcohols

J. S. Yadav, B. V. Subba Reddy, K. Premalatha, A. V. Narsaiah, S. S. Reddy

Catalysis Letters, 2009, 131, 480.

400 Addition of aryl cuprates to azides: a novel approach for the synthesis of unsymmetrical diaryl amines

J. S. Yadav, B. V. Subba Reddy, P. Borkar, P. J. Reddy



28

399 Mesoporous aluminosilicate nanocage catalyzed 3CC reaction: an expedient synthesis of µ-aminophosphonates

A. Vinu,Ϯ P.Kalita, V. V. B. Subramanian, H. Oveisi, T. Selvan, A. Mano, B. V. Subba Reddy


398 Total synthesis of (+)-Aspicilin from D-mannitol

J. S. Yadav, T. S. Rao, K. Ravindar, B. V. Subba Reddy

Synlett, 2009, 2828.

397 Cu(OTf)2/Cu-catalyzed four-component reaction: a facile synthesis of a-alkoxytriazoles via Click chemistry

J. S. Yadav, B. V. Subba Reddy, G. M. Reddy, S. Rehana Anjum


396 The stereoselective total synthesis of (1S,1'R,5'R,7'R)-1-hydroxy-exo-Brevicomin by a Chiron Approach

J. S.Yadav, K.S. Rao, B. V. Subba Reddy

Letters in Organic Chemistry 2009, 6, 4.

395 Stereoselective total synthesis of (-)-pyrenophorol

J. S. Yadav, U.V. S. Reddy, B. V. Subba Reddy


394 Iodine-catalyzed intermolecular hydroamination of vinyl arenes

J.S. Yadav, B. V. Subba Reddy, T. S. Rao, B. B. M. Krishna


393 Intramolecular-Prins-cyclization: a novel synthesis of hexahydro-2H-furo[3,2-c]pyran derivatives

J. S. Yadav, P. P. Chakravarthy, B. Prasanth, B. V. Subba Reddy, A.V. S. Sarma


392 CeCl3∙7H2O/LiI: A novel reagent system for the synthesis of N-arylpyrrolidines

J. S. Yadav, B. V. Subba Reddy, G. Narasimhulu, D. Chandrakanth, G. Sathish


391 Gallium(III) chloride catalyzed three-component coupling of naphthol, alkyne and aldehyde: a novel synthesis of 1,3-disubstituted-3H-benzo[f] chromenes

J.S. Yadav, B. V. Subba Reddy, S. Sengupta, S. K. Biswas



29

390 InBr3-catalyzed annulations of cyclic 1,3-di ketones with aryl propargyl alcohols: a novel synthesis of 2,4-diaryldihydro pyrans

J. S. Yadav, B. V. Subba Reddy, K. V. R. Rao, R. Narender


389 Immobilization of Chiral quininium salt in Ionic Liquid for enantioselective epoxidation of chalcones

R. R. Pal, R.T. Dere, P. S. Patil, B. V. Subba Reddy, M. M. Salunkhe

Letters in Organic Chemistry 2009, 332.

388 FeCl3-catalyzed functiona-lization of monoterpenes via hydroalkylation of unactivated alkenes

J. S. Yadav, B. V. Subba Reddy, G. Narasimhulu, K. V. Purnima


387 First example of C-3 alkylation of indoles with activated azetidines catalyzed by indium(III) tribromide

J. S. Yadav, B. V. Subba Reddy, G. Narasimhulu, G. Satheesh

Synlett 2009, 727.

386 Enantioselective Reduction of Prochiral Ketones Employing Sprouted Pisum sativa as Biocatalyst

J. S. Yadav, B. V. Subba Reddy, Ch. Sreelakshmi, A. Bhaskar Rao


385 Total synthesis of Xestodecalactone C from L-malic acid

J. S. Yadav, Y. Gopala Rao, K. Ravindar, B. V. Subba Reddy, A.V. Narsaiah


384 Gallium(III) Chloride Catalyzed Hydroarylation of Arylacetylenes with Naphthols and Phenols: A Facile Synthesis of Vinylarenes

J. S. Yadav, B. V. Subba Reddy, S. Sengupta, S. K. Biswas


383 Iron(III) Chloride: A versatile catalyst for the practical synthesis of 3-sulfenylindoles

J. S. Yadav, B. V. Subba Reddy, Y. J. Reddy, K. Praneeth


382 Iodine catalyzed 1,4-addition of 2-(trimethylsilyloxy)furan to α,β-unsaturated ketones: a facile synthesis of γ-butenolides

J. S. Yadav, B. V. Subba Reddy, G. Narasimhulu, N. S. Reddy, P. J. Reddy



30

381 Heteropoly acid-catalyzed aza-Prins-cyclization: an expeditious synthesis of 4-hydroxypiperidines

J. S. Yadav, B. V. Subba Reddy, D. N. Chaya, G. G. K. S. N. Kumar, P. Naresh, B. Jagadeesh


380 Three-component synthesis of 2-aryl-4-arylthio-tetrahydro-2H-pyrans via the Prins cyclization

J. S. Yadav, B. V. Subba Reddy, Y. J. Reddy, N. S. Reddy


379 First stereoselective total synthesis of Goniothalesdiol A

J. S. Yadav, N. Rami Reddy, V. Harikrishna, B. V. Subba Reddy


378 InBr3-catalyzed three-component reaction: a facile synthesis of propargyl amines

J. S. Yadav, B. V. Subba Reddy, A.V. H. Gopal, K. S. Patil

Tetrahedron Letters 2009, 3493.

377 InX3-catalyzed haloamidation of vinyl arenes: a facile synthesis of a-bromo- and a– fluoroamides

J. S. Yadav, B. V. Subba Reddy, D. N. Chary, D. Chandrakanth


376 Boron Trifluoride-Diethyl Etherate Complex Mediated Allylation of Baylis-Hillman Adducts: A Facile Synthesis of 1,5-Dienes

J. S. Yadav, B. V. Subba Reddy, S. S. Mandal, A. P. Singh, A. K. Basak


375 3CC of isoquinoline, activated alkyne and nitromethane: A facile synthesis of nitromethyl derivatives 1,2-dihydro-isoqunolines

J. S. Yadav, B. V. Subba Reddy, N. N. Yadav, M. K. Gupta


374 First Stereoselective Total Synthesis of Sporostatin and Determination of Absolute Configuration

J. S. Yadav, N. Thrimurtulu, K. Uma Gayathri, B. V. Subba Reddy, A. R. Prasad

Synlett 2009, 790.

373 Iodine-catalyzed 3CCreaction: A rapid synthesis of a-alkoxy azides and homoallyl ethers

J. S.Yadav, B. V. Subba Reddy, G. M. Reddy, R. Narender



31

372 First example of carbon-Ferrier rearrangement of glycals with isocyanides: a novel synthesis of C-glycosyl amides

J. S. Yadav, B. V. Subba Reddy, D. Narasimha Chary


371 Modular Total Synthesis of Lamellarin G Trimethyl Ether

J. S Yadav, K. Uma Gayathri, B. V. Subba Reddy, A. R. Prasad

Synlett 2009, 43.

370 Stereoselective total synthesis of xestodecalactone C and epi-sporostatin via the Prins cyclization

J. S. Yadav, N.Thrimurtulu, K. Uma Gayathri, B. V. Subba Reddy, A. R. Prasad


369 IBX/I2-mediated oxidation of alkenes and alkynes in water: a facile synthesis of a-iodoketones

J. S. Yadav, B. V. Subba Reddy, A. P. Singh, A. K. Basak


368 Indium-mediated alkynylation of Baylis-Hillman acetates: a novel route to 1,4-enynes

J. S. Yadav, B. V. Subba Reddy, N. N.Yadav, A. P. Singh, Ch. Madavi, A. C. Kunwar


367 The first stereoselective total synthesis of Leiocarpin C and the total synthesis of (+)-Goniodiol

J. S. Yadav, K. Premalatha, S. J. Harshavardhan, B. V. Subba Reddy


366 IBX: A Novel and Versatile Oxidant for Electrophilic Thiocyanation of Indoles, Pyrrole and Aryl Amines

J. S. Yadav, B. V. Subba Reddy, B. B. Murali Krishna


365 Bismuth(III)-catalyzed rapid synthesis of 2,3-disubstituted quinoxalines in water

J. S. Yadav, B. V. Subba Reddy, K. Premalatha, K. S. Shankar


364 Copper(II) tetrafluoroborate as mild and versatile catalyst for the rapid synthesis of b-acetamido ketones and esters via a three-component reaction

J. S. Yadav, B. V. Subba Reddy, K. S. Shankar, K. Premalatha

Organic Commun. 2008, 14, 76.


32

363 A stereoselective approach for the total synthesis of Clonostachydiol

J. S. Yadav, T. Swamy, B. V. Subba Reddy

Synlett 2008, 2773.

362 Indium-mediated Allylation of Heteroaryl, Benzyl and Cinnamyl Thiocyanates: A Novel Route for 3-(Allylthio)-1H-Indoles

J. S. Yadav, B. V. Subba Reddy, D. Chandrakanth, A. V. Hara Gopal

Chemistry Letters 2008, 1082.

361 Zinc-mediated allylation of aryl propargyl acetates: A facile synthesis of 1,5-enynes

J. S. Yadav, B. V. Subba Reddy, D. Chandrakanth, B. Prashant


360 Microwave-accelerated solvent and catalyst free synthesis of 3-indolyl hydroquinones

J. S. Yadav, B. V. Subba Reddy, K. S. Shankar, T. Swamy, K. Premalatha

Bull. Korean. Chem. Soc. 2008, 28, 1418.

359 Mg/CdCl2 a bimetallic catalyst system for the allylation of aldehydes with allyl bromide: An efficient protocol for the synthesis of homoallylic alcohols

A.V. Narasaiah, A. R. Reddy, Y. G. Rao, E. V. Kumar, R. S. Prakasham, B. V. Subba Reddy, J. S. Yadav


358 Aluminium(III)-promoted Prins-cyclization of 2-allylphenols: an expedient synthesis of benzoxepines

J.S. Yadav, B. V. Subba Reddy, N. N. Yadav, G. Satheesh


357 Three-component coupling of aldehyde, homoallyl alcohol & trimethylsilyl azide: a facile synthesis of 4-azidotetrahydro- pyrans via the Prins-cyclization

J. S. Yadav, B. V. Subba Reddy, T. Maity, G. G. K. S. N. Kumar


356 Gold(III) chloride catalyzed 3CC reaction: A new strategy for the synthesis of dihydroquinoline /isoquinolines


Jornal of Organic Chemistry 2008, 73, 6857.

355 Bismuth Triflate Catalyzed Prins-Ritter Reaction: An Efficient Synthesis of 4-Amidotetrahydropyrans

J. S. Yadav, B. V. Subba Reddy, D. N. Chaya, G. G. K. S. N. Kumar

Canadian Journal of Chemistry, 2008, 86, 769.


33

354 Azido-Schmidt reaction for the formation of amides, imides and lactams from ketones in the presence of FeCl3

J. S. Yadav, B. V. Subba Reddy, U. V. S. Reddy, K. Praneeth


353 The cation exchange resin promoted coupling of alkynes with aldehydes: one-pot synthesis of a,b-unsaturated ketones

J. S. Yadav, B. V. Subba Reddy, P. Vishnumurthy


352 Iodine as a mild and efficient catalyst for the diastereo-selective synthesis of d-silyloxy-g-lactone

J.S. Yadav, B. V. Subba Reddy, G. Narasimhulu, G. Satheesh

Tetrahedron Lett. 2008, 49, 5683

351 Heteropoly acid-catalyzed highly efficient alkylation of 1,3-dicarbonyl compounds with benzylic and propargylic alcohols

J. S. Yadav, B. V. Subba Reddy, T. Pandurangam, K.V. R. Rao, K. Praneeth, G. G. K. S. N. Kumar, C. Madavi, A.C.Kunwar


350 Gallium iodide/iodine as a versatile reagent for the aza-Prins cyclization: an expeditious synthesis of 4-iodopiperdines

J. S. Yadav, B. V. Subba Reddy, D. N. Chaya, G. G. K. S. N. Kumar, S. Aravind, A. C. Kunwar, Ch. Madavi


349 A novel biomimetic condensation of 2-deoxy ribose, aryl amine and acetyl acetone to bicyclic aminols catalyzed by InCl3

J. S. Yadav, B. V. Subba Reddy, G. Satheesh, G. Narasimhulu, Portier Yvan, C. Madhavi, A. C. Kunwar


348 3CC reactions of isoquinolines, dimethyl acetylene dicarboxylate and indoles: a facile synthesis of 3-indolyl-1,2-dihydro-2-isoquinolinyl-2-butenedioate



347 N-chlorosuccinimide as a versatile reagent for the sulfenylation of ketones: a facile synthesis of a-ketothioethers

J. S. Yadav, B. V. Subba Reddy, R. Jain, G. Baishya



34

346 A tandem Ferrier and Click reaction: a facile synthesis of triazolyl-2,3-dideoxy pyranosides

J. S. Yadav, B. V. Subba Reddy, D. Narasimha Chary, Ch. Suresh Reddy


345 First example of the coupling of a-diazoketones with thiourea: a novel route for the synthesis of 2-aminothiazoles

J. S. Yadav, B. V. Subba Reddy, Y. Gopala Rao, A. V. Narsaiah


344 Iodine as a mild and versatile reagent for the synthesis of 1,3-dioxane derivatives via the Prins reaction

J. S. Yadav, B. V. Subba Reddy, A. V. Hara Gopal, G. G. K. S. Narayana Kumar

Tetrahedron Lett, 2008, 49, 4420.

343 Enantioselective reduction of 2-substituted tetrahydropyran-4-ones using Daucus carota plant cells

J. S. Yadav, B. V. Subba Reddy, Ch. Sreelakshmi, G. G. K. S. Narayana Kumar, A. Bhaskar Rao


342 The silver salt of 12-tungstophosphoric acid: a mild, selective and efficient catalyst for the synthesis of b-ketoesters via C-H insertion

J. S. Yadav, B. V. Subba Reddy, K. V. Purnima, S. Jhansi, K. Nagaiah

Catalysis Communications 2008, 9, 2361.

341 FeCl3 as mild and efficient reagent for the a-thiocyanation of ketones: an expedient synthesis of a-ketothiocyanates

J. S. Yadav, B. V. Subba Reddy, U. V. Subba Reddy, D. Narasimha Chary


340 Bi(OTf)3 as mild, efficient and cost-effective catalyst for the alkylation of N-heterocycles with epoxides

J. S. Yadav, B. V. Subba Reddy, A. D. Krishna, A. Ramesh Reddy, A. V. Narsaiah


339 Stereoselective synthesis of C6-C18 fragment of Scytophycin-C using a novel synthetic methodology

J. S. Yadav, V. Sunitha, B. V. Subba Reddy, E. Gyanchander


338 Heteropoly acid as efficient, cost-effective and recyclable solid acid for the rapid synthesis of imidazolines

J. S. Yadav, B. V. Subba Reddy, T. Pandurangam, U. V. Subba Reddy



35

337 Iodine/EtOH: A Novel and Versatile Catalyst for the Synthesis of β-Amino Ketones via 3CC reaction

J. S. Yadav, B. V. Subba Reddy, K. Shiva Shankar, K. Premalatha, T. Swamy


336 Hydroamination of unactivated alkenes with sulfonamides catalyzed by phosphomolybdic acid/SiO2

J. S. Yadav, B. V. Subba Reddy, A. Raju, K. Ravindar, R. Narender

Letters in Organic Chemistry 2008, 5, 651.

335 Green protocol for conjugate addition of amines onto p-quinones accelerated by water

J. S. Yadav, B. V. Subba Reddy, T. Swamy, K. Shiva Shankar

Monatshefte für Chemie / Chemical Monthly 2008, 139, 1317.

334 Iodine as a mild, efficient and cost-effective catalyst for the synthesis of thiiranes from oxiranes

J. S. Yadav, B. V. Subba Reddy, S. Sengupta, M. K. Gupta, G. Baishya, S. J. Harshavardhana, U. Dash

Monatshefte für Chemie / Chemical Monthly 2008, 139, 1363.

333 Cu-Exchanged TPA: an efficient and reusable heteropoly acid for the cyclopropanation of alkenes via C-H insertion

J. S Yadav, B. V. Subba Reddy, K. V. Purnima, K. Nagaiah, N.Lingaiah

Journal of Molecular Catalysis A: Chemical 2008, 285, 36.

332 Total synthesis of 8-Methoxygoniodiol via Chiron approach

J. S. Yadav, B. Madhava Rao, K. Sanjeevarao, B. V. Subba Reddy

Synlett 2008, 1039.

331 Dess-Martin periodinane promoted oxidative coupling of the Baylis-Hillman adducts with silylenol ethers: a novel synthesis of cis-fused dihydropyrans

J. S. Yadav, B. V. Subba Reddy, S. S. Mandal, A. K. Basak, C. Madhavi, A. C. Kunwar

Synlett 2008, 1175.

330 First example of Cu(OTf)2-catalyzed synthesis of quinoxalines from a-diazoketones and aryl 1,2-diamines

J. S. Yadav, B. V. Subba Reddy, Y. Gopala Rao, A.V.Narsaiah

Chemistry Lett. 2008, 348.

329 SelectfluorTM as Novel and Versatile Reagent for the Rapid Thiocyanation of Indoles, Aza-indole, and Carbazole

J. S. Yadav, B. V. Subba Reddy, Y. J. S. Reddy



36

328 Three-component reaction of aldose sugars, aryl amines and 1,3-diones: a novel synthesis of annulated pyrroles

J.S.Yadav, B. V. Subba Reddy, M.Srinivas, Ch. Divyavani, J. Basha A.V. S. Sarma


327 FeCl3-catalyzed alkylation of indoles with 1,3-dicarbonyl compounds: an expedient synthesis of C-3 substituted indoles

J. S. Yadav, B. V. Subba Reddy, K. Praneeth


326 PMA-supported silica gel as efficient and cost-effective solid acid for the benzylation of indoles with benzylic alcohols

J. S. Yadav, B. V. Subba Reddy, A. Srinivas Reddy

Journal of Molecular Catalysis A Chemical 2008, 280, 219.

325 InBr3-catalyzed stereoselective synthesis of trans-2,6-di substituted 3,6-dihydro-2H-pyrans

J. S. Yadav, V. Sunitha, B. V. Subba Reddy, P. P. Das, E. Gyanchander


324 Copper(II)-catalyzed allylation of propargylic and allylic alcohols by allylsilanes a facile synthesis of 1,5-enynes

J. S.Yadav, B. V. Subba Reddy, T. Srinivasa Rao, K. V. Raghavendra Rao


323 InCl3-Catalyzed Addition of Indoles to Activated Aza-aromatic Systems

J. S.Yadav, B. V. Subba Reddy, P.Vishnumurthy, K. Premalatha


322 First example of alkynylation of propargylic alcohols with alkynylsilanes catalyzed by molecular iodine

J. S. Yadav, B. V. Subba Reddy, N.Thrimurtulu, N. M. Reddy, A. R. Prasad


321 Indium-mediated vic-diallylation/ propargylation of phenacyl bromides: a facile synthesis of 4-arylocta-1,7-dien-4-ol derivatives

J. S. Yadav, B. V. Subba Reddy, S. Kumar, Biswas, S. Sengupta


320 Three component, one-pot diastereoselective synthesis of 4-amidotetrahydropyrans via the Prins Ritter reaction sequence

J. S. Yadav, B. V. Subba Reddy, S. Aravind, G. G. K. S. N. Kumar

Tetrahedron, 2008, 64, 3025.


37

319 PMA/SiO2 as mild, efficient and cost-effective catalyst for the protection of amines with di-tert-butyldicarbonate

J. S. Yadav, Y. Gopal Rao, A. R. Reddy, A. V. Narsaiah, B. V. Subba Reddy

Letters in Organic Chemistry, 2008, 5, 116.

318 Aqueous Prins-Cyclization: A Diastereoselective Synthesis of 4-hydroxytetrahydropyran Derivatives

J. S. Yadav, B. V. Subba Reddy, G. G. K. S. N. Kumar, S. Aravind


317 One-pot oxidative allylation of Morita-Baylis-Hillman adduct with allyltrimethylsilane promoted by DMP/BF3.OEt2



316 PMA/SiO2 catalyzedamidation of alcohols with nitriles: a simple, cost-effective and recyclable catalytic system for Ritter reaction

J. S. Yadav, B. V. Subba Reddy, T. Pandurangam, Y. J. Reddy, M. K. Gupta

Catalysis Communications 2008, 9, 1297.

315 Mild and efficient conversion of aldehydes to gem-diacetates using 2nd Generation Ionic Liquids

J.S. Yadav, B. V. Subba Reddy, P. Sreedhar, G. Kondaji, K. Nagaiah

Catalysis Commun, 2008, 9, 590.

314 Bismuth(III)-catalyzed rapid and highly efficient synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles in water

J. S. Yadav, B. V. Subba Reddy, K. Premalatha, K. S. Shankar


313 In(OTf)3-catalyzed synthesis of 4-thiocyanotetrahydro pyrans via a three-component reaction

J. S. Yadav, B. V. Subba Reddy, T. Maity, G. G. K. S. N. Kumar


312 First examples of cyclizations of glucal with enamines leading to oxa-aza bicyclo nonene scaffolds

J. S. Yadav, B. V. Subba Reddy, M. Srinivas, Ch. D. Vani, A. C. Kunwar, C. Madhavi


311 Three component, regio-selective, one-pot synthesis of b-hydroxy triazoles from epoxides via Click Reaction

J. S. Yadav, B. V. Subba Reddy, G. M.Reddy, D. N. Chary



38

310 Deoxygenative allylation of benzyl acetates and cinnamyl alcohols catalyzed by molecular iodine

J. S. Yadav, B. V. Subba Reddy, A. S. Reddy, B. Eeshwaraiah


309 Hydrothiolation of unactivated alkynes catalyzed by Indium(III) bromide

J. S. Yadav, B. V. Subba Reddy, A. Raju, K. Ravindar, G. Baishya


308 Heteropoly acid-catalyzed direct substitution of propargylic alcohols with sulfonamides

J. S. Yadav, B. V. Subba Reddy, T. S. Rao, B. B. M. Krishna, G. G. K. S. N. Kumar


307 Novel coupling of a-diazo compounds with aza-aromatic systems under solvent-free conditions

J. S. Yadav, B. V. Subba Reddy, M. K. Gupta, U. Dash, D. C. Bhunia and Sk. S. Hossain

Synlett, 2007, 2801.

306 InBr3-catalyzed rapid propargylation of hetero aromaticsystems with a-aryl-substituted propargyl alcohols

J. S. Yadav, B. V. Subba Reddy, K. V. R. Rao, G. G. K. S. N. Kumar


305 First example of C-3 alkylation of indoles with cyclopropyl ketones promoted by CeCl3.7H2O/LiI

J. S. Yadav, B. V. Subba Reddy, D. Chandrakanth, G. Satheesh


304 First diastereoselective synthesis of 4-azido-tetra hydropyrans via Prins-cyclization

J. S. Yadav, B. V. Subba Reddy, T.Maity, G. G. K. S. N. Kumar


303 IBX/Sc(OTf)3-promoted one-pot oxidative conjugate addition of allyltrimethylsilane to Baylis-Hillman adducts

J. S. Yadav, B. V. Subba Reddy, A.P. Singh, A.K. Basak


302 Cu(OTf)2-catalyzed synthesis of imidazo[1,2]pyridines from a- diazoketones and 2-aminopyridines

J. S. Yadav, B. V. Subba Reddy, Y. G.Rao, M. Srinivas, A. V. Narsaiah


301 PMA/SiO2 as efficient, cost-effective and recyclable catalytic system for synthesis of highly substituted pyrroles

J. S. Yadav, B. V. Subba Reddy, T. S. Rao, R. Narender, M. K. Gupta

Journal of Molecular Catalysis A, 2007, 278, 42.


39

300 Iodine-catalyzed coupling of 4-hydroxyproline with isatins: an expeditious synthesis of 3-pyrrolyl indolin-2-ones

J. S. Yadav, B. V. Subba Reddy, R. Jain, U. V. S. Reddy

Journal of Molecular Catalysis A, 2007, 278, 38.

299 SelectfluorTM as novel and efficient reagent for the sufenylation of indoles: a rapid synthesis of 3-sufenyl indoles

J. S. Yadav, B. V. Subba Reddy, Y. J. S. Reddy


298 InBr3 as versatile and highly efficient catalyst for the synthesis of 3-allyl- and 3-benzylindoles

J. S. Yadav, B. V. Subba Reddy, S. Aravind, G. G. K. S. N. Kumar, A. S. Reddy


297 Indium-mediated allylation/ propargylation of a-diazo ketones: a facile synthesis of 1-bromo-2-alkyl- or 2-aryl- pent-4-en-2-ols

J. S. Yadav, B. V. Subba Reddy, P. V. Murty, S. K. Biswas


296 Cation -exchange resin as efficient, cost-effective and recyclable catalyst for the synthesis of 3-propargyl indoles

J. S. Yadav, B. V. Subba Reddy, G. G. K. S. N. Kumar, K. V. R. Rao

Chemistry Letters, 2007, 942.

295 Total synthesis of diospongin A via an enzymatic resolution of (±)-tetrahydropyranol derived from Prins cyclization

J. S.Yadav, B. P. Vani, B. V. Subba Reddy, Ch. Venugopal, A. B. Rao

Synlett, 2007, 2045.

294 A formal stereoselective total synthesis of (-)-Maurenone

J. S. Yadav, K. Ravindar, B. V. Subba Reddy

Synlett, 2007, 1957.

293 SelectfluorTM as novel and efficient reagent for the 1,4-addition of indoles to a,b-unsaturated ketones

J. S. Yadav, B. V. Subba Reddy, A. Raju, K. Ravindar, G.Baishya


292 Iodine as mild, efficient and cost-effective for the synthesis of cis-dihydroisoquinolin-1-one-4-carboxylic acids

J. S. Yadav, B. V. Subba Reddy, A. R. Reddy, A. V. Narsaiah



40

291 First one-pot oxidative Michael reaction of Baylis-Hillman adducts with indoles promoted by 2-iodoxy benzoic acid



290 Organic synthesis in water: Green protocol for the synthesis of 2-amino furan derivatives

J.S. Yadav, B. V. Subba Reddy, S. Shubashree, K. Sadashiv, D. K. Rao


289 Amberlyst A-21âas efficient and recyclable heterogeneous catalyst for the synthesis of substituted 4H-chromenes

J. S. Yadav, B.V. Subba Reddy, M. K. Gupta, I. Pratap, S. K. Pandey

Catalysis Commun, 2007, 8, 2208.

288 First stereoselective total synthesis of ophiocerins B & C

J. S. Yadav, P.N. Lakshmi, S. J. H. Vardhan, B. V. Subba Reddy

Synlett, 2007, 12, 1945.

287 CeCl3∙7H2O/AcCl-catalyzed Prins Ritter reaction sequence: a novel synthesis of 4-amido tetrahydropyran derivatives

J. S. Yadav, B. V. Subba Reddy, G. G. K. S. N. Kumar, G.M.S. Reddy


286 Bi(OTf)3-catalyzed condensation of 2,2-DMP with aromatic amines: a rapid synthesis of 2,2,4-trimethyl-1,2-dihydroquinolines

J. S. Yadav, B. V. Subba Reddy, K. P. Latha, M.S. R.Murthy


285 Iodine/MeOH as novel and versatile reagent system for the synthesis of a-ketothiocyanates

J.S. Yadav, B. V. Subba Reddy, U. V. S. Reddy, A. D. Krishna


284 LiBF4-Catalyzed 3CC of aldehyde, acetic anhydride and allyltrimethylsilane/ TMSCN

J.S. Yadav, B. V. Subba Reddy, P. V. Murthy, Ch. J. Chary

Tetrahedron Lett. 2007 , 48, 5915.

283 InBr3-catalyzed cleavage of cyclic and acyclic ethers: an efficient and practical ring opening reaction

J.S. Yadav, B. V. Subba Reddy, M. K. Reddy, U.Dash, M. K. Gupta


282 Enzymatic kinetic resolution of racemic 4-tetrahydro pyranols by Candida rugosa

J. S. Yadav, B. V. Subba Reddy, B.P.Vani, Ch. Venugopal, A.B. Rao



41

281 Microwave accelerated SN2' substitution of Baylis-Hillm- an acetates: a comparative study of conventional heating vs microwave irradiation

J.S.Yadav, B. V. Subba Reddy, A.K.Basak, A.V.Narsaiah


280 Sc(OTf)3-catalyzed alkylation of indoles with propargyl alcohols: an expeditious synthesis of 3-substituted indoles

J.S. Yadav, B. V. Subba Reddy, K. V. R. Rao, G. G. K. S. N. Kumar


279 Ionic Liquid accelerated Pet- asis reaction: a green protocol for the synthesis of alkyl- aminophenols

J.S. Yadav, B. V. Subba Reddy, P.N. Lakshmi

Journal of Molecular Catalysis A: Chemical 2007, 274,101.

278 InCl3/H2O a versatile catalytic system for the synthesis of C-furyl glycosides & trihydroxy alkyl furans

J. S. Yadav, B. V. Subba Reddy, M.Srinivas, G.Satheesh

Synthesis, 2007, 11, 1712.

277 Iodine-promoted Prins cyclization of ketones: A facile synthesis of spirocyclic-4-iodotetrahydropyrans and 5,6-dihydro-2H-pyrans

J.S. Yadav, B. V. Subba Reddy, V. H. Krishna, T. Swamy, G. G. K. S. N. Kumar


276 Organic synthesis in water: Green protocol for the conjugate addition of thiols to p-quinones

J.S.Yadav, T. Swamy, B. V. Subba Reddy, D. K. Rao

J. Mol. Catalysis A: Chemical 2007, 274, 116.

275 Sm(III) triflate-catalyzed conjugate addition of amines to electron-deficient olefins

J.S. Yadav, A. R.Reddy, Y. G. Rao, A.V. Narsaiah, B. V. Subba Reddy


274 3CC reactions in ionic liquids: One-pot synthesis of isoxazolidines

J.S. Yadav, B. V. Subba Reddy, P. Sreedhar, Ch.V.S.R. Murthy, G. M. Kumar, G. Kondaji, K. Nagaiah

J. Mol. Catalysis A: Chemical 2007, 160.

273 Dy(OTf)3 as a versatile catalyst for the synthesis of 3-pyrrolylindolinones and pyrrolylindeno[1,2-b]quino-xalines

J.S.Yadav, B. V. Subba Reddy, R. Jain, Ch.S.Reddy



42

272 Facile addition of ketones to activated isoquinolines using N-methyl-2-pyrrolidinone

J.S.Yadav, B. V. Subba Reddy, M.K. Gupta, I. Prathap, U. Dash


271 Green protocol for Willgerodt-Kindler transformation using [bmim]BF4 ionic medium

J.S.Yadav, B. V. Subba Reddy, G. Kondaji, J.S.S.Reddy, K. Nagaiah


270 Iodine as a versatile reagent for the Prins cyclization: an expeditious synthesis of 4-iodotetrahydropyran derivatives

J.S.Yadav, B. V. Subba Reddy, G.G.K.S.Narayana Kumar, T. Swamy


269 Gallium(III) Chloride catalyzed stereoselective synthesis of E-configured α,β-unsaturated ketones

J.S.Yadav, B. V. Subba Reddy, M. K.Gupta, U.Dash, S.K.Pandey

Synlett 2007, 809.

268 CeCl3·7H2O/IBX-promoted oxidation of 3-alkylindoles to 3-hydroxyoxindoles

J.S.Yadav, B. V. Subba Reddy, Ch.S. Reddy, A.D.Krishna


267 CeCl3·7H2O/LiI: A novel reagent system for the synthesis of 4-iodotetrahydro pyrans via Prins cyclization

J.S.Yadav, B. V. Subba Reddy, G.G.K.S.N. Kumar, G.Madhusudhan Reddy


266 Indium(III) chloride/2-Iodoxy benzoic acid: A novel reagent system for the conversion of indoles into isatins

J.S.Yadav, B. V. Subba Reddy, Ch.S.Reddy, A.D. Krishna


265 GaCl3-Catalyzed addition of thiols to glycals: a facile synthesis of 2-deoxy thioglycosides

J.S.Yadav, B. V. Subba Reddy, E.V. Bhasker, S. Raghavendra, A.V.Narsaiah,


264 GaI3-promoted stereoselective aldol coupling of a,b-acetylenic ketones

J.S.Yadav, B. V. Subba Reddy,M. K. Gupta, S. K. Pandey


263 An efficient protocol for ring opening of epoxides by Sm(OTf)3 Synthesis of Propranolol, Atenolol and R0363

J.S.Yadav, A. R. Reddy, A. V. Narsaiah, B. V. Subba Reddy

J. Mol.Catalysis A: Chemical 2007, 261, 207.


43

262 TPP: An Efficient Catalyst for

Transesterification of b-Ketoesters

J. S. Yadav, B. V. Subba Reddy, A. D. Krishna, Ch. S. Reddy, A. V. Narsaiah.

J. Mol.Catalaysis A: Chemical, 2007, 261, 93.

261 Efficient protocol for reductive amination of aldehydes and ketones with sodium borohydride in an ionic liquid/H2O system

K. Nagaiah, V.N.Kumar, R.S Rao, B. V. Subba Reddy, A.V.Narsaiah, J.S.Yadav

Synthetic Communications 2006, 3345.

260 IBX: An efficient and novel oxidizing agent for the aromatization of 1,4-dihydropyridines

J.S.Yadav, B. V. Subba Reddy, A. V. Narsaiah, A. K. Basak, G. Baishya


259 Indium tribromide: an efficient catalyst for the silylation of hydroxyl groups by activating HMDS

J.S.Yadav, B. V. Subba Reddy, A.K.Basak, G.Baishya & A.V. Narsaiah

Synthesis 2006, 3831

258 LiClO4-accelerated cleavage of aziridines with thiols: A facile synthesis of b-amino sulfides

J.S.Yadav, B. V. Subba Reddy, G. Baishya, P. V. Reddy, A.V. Narsaiah

Catalysis Communications. 2006, 7, 807.

257 Bi(OTf)3-catalyzed condensation of isatin with indoles & pyrroles: a facile synthesis of 3,3-diindolyl- and 3,3-dipyrrolyl oxindoles

J.S.Yadav, B. V. Subba Reddy, Sd. Meraz, K.Uma Gayatri, A. R. Prasad


256 Montmorillonite KSF clay catalyzed stereoselective synthesis of 2,4-disubstituted tetrahydro-quinolines

J.S.Yadav, B. V. Subba Reddy, S. Meraz, P. V. Murthy, K. Narsimulu, A. C. Kunwar


255 Intramolecular imino-Diels-Alder reactions in [bmim]BF4

ionic medium: Green protocol for the synthesis of tetrahydrochromano- quinolines

J. S.Yadav, B. V. Subba Reddy, G. Kondaji, S. Sowjanya, K. Nagaiah

Journal of Mol. Catalysis A: Chemical 2006, 258, 361.

254 CeCl3.7H2O/NaI- promoted efficient alkylation of activated quinoline and isoquinoline

J. S. Yadav, B. V. Subba Reddy, K. Sathaiah, & P. N. Reddy



44

253 Sc(OTf)3 catalyzed highly rapid and efficient synthesis of b-enamino compounds under solvent-free conditions

J.S. Yadav, V. N.Kumar, R. S. Rao, A. D. P.Darshini, P. P. Rao, B. V. Subba Reddy, K. Nagaiah

J. Mol. Catalysis A: Chemical, 2006, 256, 234.

252 Novel acetoxylation and C-C coupling reactions at unactivated positions in a-amino acid derivatives

B. V. Subba Reddy, L. R. Reddy, E. J. CoreyϮ

Organic Lett. 2006, 8, 3391.

251 Efficient method for selective introduction of substituents as C-(5) of Isoleucine and other a-amino acids

L. R. Reddy, B. V. Subba Reddy, E. J. CoreyϮ

Organic Letters 2006, 8, 2819.

250 Reaction of orthoesters with alcohols in the presence of acidic catalysts: A study

H. M. S. Kumar, Sipak J, B. V. Subba Reddy, P.P. Chakravarthy, A. D. Krishna, J. S. Yadav

Indian J. Chemistry, 2005, 44, 1686.

249 First Example of Functionalization of Activated Quinolines by Indoles using CeCl3.7H2O

J.S.Yadav, B. V. Subba Reddy, K.Sathaiah & P.Vishnumurthy

Synlett, 2005, 2811.

248 CeCl3·7H2O/NaI-Promoted Stereoselective Aldol Coupling of a,b-Acetylenic Ketones

J. S. Yadav, B. V. Subba Reddy, M. K. Gupta, B. Eeshwaraiah


247 GaX3 Promoted synthesis of 1,3,5-triaryl-1,5-dihalo-1,4-pentadienes

J.S. Yadav, B. V. Subba Reddy, B. Eeshwaraiah, M.K Gupta, S. K. Biswas


246 An Efficient, Stereocontrolled Synthesis of a Potent Omuralide-Salinosporin Hybrid for the selective Proteasome Inhibition

L. R. Reddy, J. F. Fouernier, B. V. Subba Reddy, E .J. CoreyϮ

J. Am. Chem. Soc. 2005, 127, 8974.

245 New Synthetic Route for the Enantioselective Total Synthesis of Salinosporamide A and Biologically Active Analogues

L. R. Reddy, J. F. Fouernier, B. V. Subba Reddy, E .J. CoreyϮ

Organic Lett. 2005, 7, 2699.


45

244 Simple Enantiospecific Syntheses of the C(2)-Diastereomers of Omuralide and 3-Methylomuralide

L. R. Reddy, P.Sarvanan, J. F. Fouernier, B. V. Subba Reddy, E. J. CoreyϮ

Organic Lett. 2005 7, 2703.

243 Dimethylaluminium methyl tellurate, a new reagent for the cleavage of hindered methyl esters under exceptionally mild conditions by a novel mechanism

B. V. Subba Reddy, L. R. Reddy, E .J. CoreyϮ

Tetrahedron Lett. 2005 46, 4589.

242 Mild and Efficient method for the cleavage of cyclic and acyclic ethers by Iodine under solvent-free conditions

J. S. Yadav, B. V. Subba Reddy, P.M. K. Reddy, M. K. Gupta


241 Zn/[bmim]PF6 mediated Markovnikov allylation of unactivated terminal alkynes

J. S. Yadav, B. V. Subba Reddy, P.M. K. Reddy, M. K.Gupta


240 LiClO4-Catalyzed Regioselective Ring-Opening of Aziridines with Potassium Thiocyanate

J. S. Yadav, B. V. Subba Reddy, B. Jyothirmai, M.S.R.Murthy


239 Co2(CO)8 as a novel and water-tolerant reagent to the conversion of azide to amines in aqueous media

J. S. Yadav, B. V. Subba Reddy, G. Satheesh, K. R. Rao


238 Nucleophilic displacement by azide and cyanide on Baylis-Hillman acetates

J .S. Yadav, M. K. Gupta, S. K. Pandey, B. V. Subba Reddy, A.V.S. Sarma


237 Conjugate addition of Indoles to a,b-unsaturated ketones using Cu(OTf)2-immobilized in [bmim]BF4

J.S. Yadav, B. V. Subba Reddy, G. Baishya, K. V. Reddy, A. V. Narsaiah


236 Montmorillonite KSF clay as novel and recyclable hetero-geneous solid acid for the conversion of D-glycals into furan diol

J.S.Yadav, B. V. Subba Reddy, A.V. Madhavi

Journal Mol.Catalysis A Chemical 2005, 226, 213.


46

235 Allylation and cyanation of aza-aromatics activated by chloroformate and a catalytic amount of iodine

J.S. Yadav, B. V. Subba Reddy, M. Srinivas, G. Sathaiah


234 Facile addition of alkynes to aza-aromatic systems: a new protocol for the preparation of 2-alkynyl-1,2-dihydro quinolines

J. S. Yadav, B. V. Subba Reddy, M. Sreenivas, K. Sathaiah


233 NbCl5: An efficient Lewis acid catalyst for selective acetylation of alcohols and phenols

J. S. Yadav, A. V. Narsaiah, B. V. Subba Reddy, K. Nagaiah

Jornal Mol.Catalysis A: Chemical 2005, 226, 107.

232 Green approach for the conversion of olefins into vic-halohydrins using N-halo succinimides in ionic liquids

J. S. Yadav, B. V. Subba Reddy, G. Baishya, S. J.Harshavardhan, Ch. J. Chary


231 CBr4-catalyzed regioselective ring opening of epoxides with alcohols and water

J. S. Yadav, B. V. Subba Reddy, K.Harikishan, Ch. Madan, A. V. Narsaiah


230 InCl3-catalyzed stereoselective synthesis of 1,5-benzodiazepines

J.S. Yadav, B. V. Subba Reddy, G. Satheesh, G. Srinivasulu, A. C. Kunwar

ARKIVOC, 2005, 3, 221.

229 NbCl5 as novel and efficient Lewis acid for tetrahydropyranylation of alcohols and phenols

K. Nagaiah, B. V. Subba Reddy, D.Sreenu, A. V.Narsaiah

ARKIVOC, 2005, 3, 192.

228 First example of C-alkylation of indoles with Baylis-Hillman acetates

J. S. Yadav, B. V. Subba Reddy, A. K. Basak, A. V. Narsaiah, A.Prabhakar, B.Jagadeesh


227 Ionic Liquid accelerated intramolecular hetero-Diels-Alder reactions: a protocol for the synthesis of octahydro-acridines

J. S. Yadav, B. V. Subba Reddy, Lakshindra Chetia, G. Srinivasulu, A. C. Kunwar



47

226 NbCl5-catalyzed C-H insertion reactions of a-diazoesters: a facile synthesis of b-keto esters

J. S. Yadav, B. V. Subba Reddy, B. Eeshwaraiah, P. N. Reddy


225 Cu(OTf)2 immobilized in [bmim]BF4 Ionic Liquid: An efficient reaction medium for Michael addition of b-keto esters and acceptor-Activated alkenes

J.S.Yadav, B. V. Subba Reddy, G. Baishya, A. V. Narsaiah


224 InBr3: a novel and efficient reagent for the rapid synthesis of 1,5-benzodiazepines under solvent-free conditions

J. S. Yadav, B. V. Subba Reddy, S. Praveenkumar, K. Nagaiah


223 First example of activation of PMHS with molecular iodine: a facile synthesis of 3,6-dihydropyran derivatives

J. S. Yadav, B. V. Subba Reddy, K. Premalatha, T.Swamy


222 Amberlyst-15Òas novel and recyclable solid acid for the coupling of aromatic aldehydes with homopropargyl alcohol

J.S.Yadav, B. V. Subba Reddy, P.Vishnumurthy


221 Chemoselective allylation of aldehydes using CeCl3.7H2O: a facile synthesis of homo allylic alcohols

J.S. Yadav, B. V. Subba Reddy, G. Kondaji, J. S. Sunder Reddy


220 FeCl3-promoted electrophilic thiocyanation of aromatic and heteroaromatic compounds

J.S. Yadav, B. V. Subba Reddy, A.D. Krishna, Ch.Suresh Reddy


219 Ionic liquids/H2O systems for the reaction of epoxides with NaN3: a new protocol for the synthesis of 2-azidoalcohols

J.S. Yadav, B. V. Subba Reddy, B. Jyothirmai M.S.R. Murty


218 First example of ring expansion of activated quinolines & iso-quinolines: novel benzoazepines

J. S. Yadav, B. V. Subba Reddy, M K. Gupta, A. Prabhakar, B. Jagadeesh

Chem. Commun. 2004, 2124.


48

217 Rapid and Efficient Protocol for the Synthesis of 4-Chloro-tetrahydropyrans using NbCl5

J. S. Yadav, B. V. Subba Reddy, M. K. Gupta, S. K. Biswas


216 GaCl3-catalyzed coupling of indoles with phenyl acetylene: synthesis of bis(indolyl)- phenylethanes

J. S. Yadav, B. V. Subba Reddy, B. Padmavani, M. K. Gupta


215 First example of molecular iodine-catalyzed allylation and alkynylation of cyclic allylic acetates

J.S. Yadav, B. V. Subba Reddy, K. V. Rao, K. Sarita Raj, P. P. Rao, A. R. Prasad, D. Gunasekar


214 Rapid and efficient synthesis of optically active pyrazoles under solvent-free conditions

J. S. Yadav, B. V. Subba Reddy, G. Satheesh, P. N. Lakshmi, S. K. Kumar, A. C. Kunwar


213 InCl3/SiO2-catalyzed a-amination of 1,3-dicarbonyl compounds under microwave irradiation

J.S. Yadav, B. V. Subba Reddy, Ch. Venugopal, B. Padmavani


212 Bi(OTf)3-[Bmim]PF6: A novel and recyclable catalytic system for the diasteroselective synthesis of cis-fused pyrano & furanobenzopyrans

J. S. Yadav, B. V. Subba Reddy, P. N. Reddy


211 NbCl5-catalyzed rapid and efficient synthesis of 3,4-dihydro-pyrimidinones

J.S.Yadav, B. V. Subba Reddy, Jaishri J. Naidu, and K.Sadashiv


210 FeCl3-Promoted efficient thiocyanation of aryl alkenes: A facile synthesis of dithiocyanates

J.S.Yadav, B. V. Subba Reddy, Manoj Kumar Gupta


209 Ag3PW12O40: a novel and recyclable heteropoly acid for Friedländer quinoline synthesis

J.S.Yadav, B. V. Subba Reddy, P. Sreedhar, R. S. Rao, K. Nagaiah



49

208 A Novel and Efficient Method for the Synthesis of a-Azido ketones and a-Keto thiocyanates

J. S. Yadav, B. V. Subba Reddy, M. Srinivas


207 Bi(OTf)3/[bmim]BF4 as novel and reusable catalytic system for the synthesis of furan, pyrrole and thiophene derivatives

J.S.Yadav, B. V. Subba Reddy, B.Eeshwaraiah, M. K. Gupta


206 Montmorillonite KSF-catalyzed one-pot synthesis of Hexahydro-1H-pyrrolo [3,2-c] quinoline derivatives

J.S. Yadav, B. V. Subba Reddy, K. S. Reddy,V. Sunitha, K.V.S.Ramakrishna


205 Montmorillonite KSF clay-promoted synthesis of enantio-merically pure 5-substituted pyrazoles from 2,3-dihydro-4H-pyran-4-ones

J.S. Yadav, B. V. Subba Reddy, M. Srinivas, A.Prabhakar, B.Jagadeesh


204 Bi(OTf)3-catalyzed acylation of p-quinones: a facile synthesis of acylated hydroquinones

J. S. Yadav, B. V. Subba Reddy, T. Swamy, K.Raghavender Rao


203 Green protocol for the synthesis of vic-halohydrins from oxiranes using the [Bmim]PF6/LiX

J.S.Yadav, B. V. Subba Reddy, Ch. Srinivas Reddy, K. Rajasekhar


202 Ionic Liquids-promoted addition of arylsulfinic acids to p-quinones: A green synthesis of diaryl sulfones

J. S. Yadav, B. V. Subba Reddy, T. Swamy, N. Ramireddy


201 Bi(OTf)3-catalyzed Friedländer heteroannulation: a rapid synthesis of 2,3,4-trisubstituted quinolines

J.S.Yadav, B. V. Subba Reddy, K. Premalatha

Synlett, 2004, 963.

200 InCl3/IBX: A novel reagent system for the conversion of glycals into a,b-unsaturated d-lactones

J. S. Yadav, B. V. Subba Reddy, Ch. Suresh Reddy



50

199 Montmorillonite KSF clay catalyzed alkylation of pyrroles and indoles with cyclic hemi-acetals

J.S. Yadav, B. V. Subba Reddy, G. Satheesh


198 Domino Knoevenagel-hetero-Diels-Alder reactions: a stereo selective synthesis of sugar fused furo [3,2-b] pyrano[4,3-d]pyran derivatives

J. S. Yadav, B. V. Subba Reddy, D. N. Swamy, P. N. Lakshmi, K. Narsimulu, G. Srinivasulu, A. C. Kunwar


197 Ionic Liquids promoted multi-component reaction: Green approach for highly substituted 2-aminofuran derivatives

J.S. Yadav, B. V. Subba Reddy, S. Shubashree, K.Sadashiv, Jaisree J. N


196 Efficient halogenation of aromatic systems using N-halosuccinimdes in Ionic Liquids

J.S. Yadav, B. V. Subba Reddy, Reddy, PSR, Basak, A.K, Narsaiah, A.V

Adv. Synth. & Cat. 2004, 346, 77.

195 First Example of Ionic Liquids-Promoted Domino Knoevenagel Hetero-Diels-Alder Reactions: A Facile Synthesis of Pyrano[3,2-c]coumarins

J.S.Yadav, B. V. Subba Reddy, V. N. Kumar, R. Srinivas Rao, K. Nagaiah


194 Ag3PW12O40: a novel recyclable heteropoly acid for the synthesis of 1,5-benzodiazepinesunder solvent-free conditions

J. S. Yadav, B. V. Subba Reddy, S. P. Kumar, K.Nagaiah, N. Lingaiah, P. S.

Saiprasad


193 CeCl3.H2O/NaI-promoted

stereoselective synthesis of chiral 2,4-disubstituted trahydroquinolines

J.S.Yadav, B. V. Subba Reddy, M. Srinivas, B. Padmavani


192 Iodine/MeOH: a novel and efficient reagent system for thiocyanation of aromatics

J.S.Yadav, B. V. Subba Reddy, S.Shubashree, K.Sadashiv


191 Green protocol for Biginelli reaction: Ag3PW12O40 as novel and water tolerant heteropoly acid for the synthesis of 3,4-Dihydropyrimidinones

J.S. Yadav, B. V. Subba Reddy, P.Sridhar, J.S.S. Reddy,

K. Nagaiah, N. Lingaiah,

P.S.Saiprasad

Eur. J. Org. Chem. 2004, 552.


51

190 InCl3-Catalyzed tandem Michael/Friedel-Crafts cyclization: a novel protocol for chiral 2,4-disubstituted tetrahydroquinolines

J.S. Yadav, B. V. Subba Reddy, B. Padmavani


189 Acylative cleavage of aziridines with acid anhydrides catalyzed by Sc(OTf)3

J. S. Yadav, B. V. Subba Reddy, K. Sadasiv, K. Harikishan, A. V. Narsaiah

Journal Mol. Catalysis: A 2004, 220, 153.

188 [Bmim]PF6/CuBr: A novel and recyclable catalytic system for the synthesis of propargyl amines

J. S. Yadav, B. V. Subba Reddy, V. N. Kumar, R.S. Rao, K. Nagaiah

New. J. Chemistry 2004, 28, 335.

187 Montmorillonite KSF clay catalyzed one-pot synthesis of a-aminonitriles

J.S. Yadav, B. V. Subba Reddy, B. Eeshwaraiah, M. Srinivas


186 Baeyer-Villiger Oxidations in Ionic Liquids: A Facile Conversion of Ketones to Esters and Lactones

J. S. Yadav, B. V. Subba Reddy, A. K. Basak, A. V. Narsaiah

Chemistry Lett. 2004, 33, 248.

185 Bi(OTf)3 catalyzed condensation of d-hydroxy-a,b-unsaturated aldehydes with aryl amines

J. S. Yadav, B. V. Subba Reddy, G. Parimala, A. K. Raju


184 Recyclable 2nd generation ionic liquids as green solvents for the oxidation of alcohols with IBX

J. S. Yadav, B. V. Subba Reddy, A. K. Basak, A.V.Narsaiah


183 Rh2(OAc)4 immobilized in [bmim]PF6: a novel and recyclable catalytic system for the cyclopropanation of alkenes

J. S. Yadav, B. V. Subba Reddy, P. N. Reddy

Adv. Syn. & Catalysis 2004, 346, 53.

182 Montmorillonite KSF and SiO2 as novel and recyclable solid acids for the synthesis of b-aminohalides and b-azidoamines

J. S. Yadav, B. V. Subba Reddy, K. Sadashiv, S. Raghavendra, K. Harikishan

Catalysis Commun. 2004, 5, 111.


52

181 Eco-friendly heterogeneous solid acids as novel and recyclable catalysts in ionic medium for tetrahydropyranols

J. S. Yadav, B. V. Subba Reddy, M. Sridhar Reddy, N. Niranjan

J. Mol.Catalysis A: Chemical 2004, 99.

180 TPP-Catalyzed Knoevenagel Condensation: A Facile Synthesis of a-Cyanoacrylates and a-Cyanoacrylonitriles

J.S. Yadav, B. V. Subba Reddy, A. K. Basak, B.Visali, A. V. Narsaiah, K.Nagaiah

Eur. J. Org. Chem. 2004, 546.

179 Bi(OTf)3 as Novel and Efficient Catalyst for the Stereoselective Synthesis of C-Pseudoglycals

J. S. Yadav, B.V.Subba Reddy, K. Srinivas Reddy, L. Chandraiah, V.Sunitha


178 SelectfluorTM : a novel and efficient reagent for the synthesis of b-hydroxy thiocyanates

J. S. Yadav, B. V. Subba Reddy,


177 Bi(OTf)3 as Novel and Efficient Catalyst for the Synthesis of b-Aminosulfides

J. S. Yadav, B. V. Subba Reddy, Gakul Baishya


176 InBr3-Catalyzed conjugate addition of indoles to p-quinones: an efficient synthesis of 3-indolyl quinones

J. S. Yadav, B. V. Subba Reddy, T. Swamy


175 Green protocol for the O-H insertion of a-diazoketones with alcohols and water using Ionic Liquid [Bmim] BF4

J. S. Yadav, B. V. Subba Reddy, M. Srinivas

Chemistry Lett. 2003, 32, 1060

174 Bi(OTf)3-catalyzed conjugate addition of indoles to p-quinones: a facile synthesis of 3-indolyl quinones



173 InBr3-Catalyzed alkynylation and allylation of acid chlorides: a facile synthesis of alkynyl and allyl ketones

J.S.Yadav, B. V. Subba Reddy, M. Sridhar Reddy, G. Parimala


172 InBr3-Catalyzed novel cyclization of glycals with aryl amines

J.S.Yadav, B. V. Subba Reddy,

K.V.Rao, K.S. Raj, A.R.Prasad,

S. K. Kumar, A. C. Kunwar, P. Jayaprakash, B.Jagannadh

Angew. Chem. Int. Engl. 2003, 42, 5198.


53

171 Microwave-accelerated conjugate addition of aldehydes to a,b-unsaturated ketones

J. S. Yadav, K. Anuradha, B. V. Subba Reddy, B. Eeshwaraiah


170 [Bmim]PF6/RuCl3.xH2O: A novel and recyclable catalytic system for the oxidative coupling of b-naphthols

J. S. Yadav, B. V. Subba Reddy, K.Uma Gayathri, A.R. Prasad

New Journal of Chemistry, 2003, 1684.

169 Aza-Michael reactions in ionic liquids: a facile synthesis of b-amino compounds

J. S. Yadav, B. V. Subba Reddy, A.K. Basak, A.V. Narsaiah


168 Novel use of SelectfluorTM for the synthesis of cis-fused pyrano- and furano-tetrahydroquinolines

J. S. Yadav, B. V. Subba Reddy, V. Sunitha, K.S. Reddy


167 Glaser oxidative-coupling in ionic liquids: an improved synthesis of conjugated 1,3-diynes

J. S. Yadav, B. V. Subba Reddy, K. B. Reddy, U. Gayatri, A.R.Prasad


166 Green protocol for conjugate addition of thiols to a,b-unsaturated ketones using [Bmim]PF6/H2O

J. S. Yadav, B. V. Subba Reddy, Gakul Baishya

J. Org. Chem. 2003, 68, 7098.

165 LiClO4-catalyzed highly diastereoselective synthesis of cis-aziridine carboxylates

J.S. Yadav, B. V. Subba Reddy, M. S. Rao, P. N. Reddy


164 [Bmim]BF4 ionic liquid: A novel and recyclable reaction media for the synthesis of vic-diamines

J.S. Yadav, B. V. Subba Reddy, K. Premalatha


163 Chemoselective 1,3-oxathio- and 1,3-dithio-acetalization of aldehydes in ionic liquids

J.S. Yadav, B. V. Subba Reddy, G. Kondaji


162 Elemental iodine -catalyzed coupling of alkynylsilanes with acid chlorides: A facile synthesis of a,b-acetylenic ketones

J.S.Yadav, B. V. Subba Reddy, M. Sridhar Reddy

Synlett, 2003, 1722.


54

161 Bi(OTf)3-[Bmim]PF6: A novel

and reusable catalytic system for the synthesis of cis-aziridine carboxylates

J. S. Yadav, B. V. Subba Reddy, P. N. Reddy, M.Shesha Rao


160 Bi(OTf)3-catalyzed allylation of epoxides: A facile synthesis of homoallylic alcohols

J. S. Yadav, B. V. Subba Reddy, G. Satheesh


159 Microwave-assisted one pot synthesis of 2,4-disubstituted quinolines under solvent-free conditions

J. S. Yadav, B. V. Subba Reddy, V. N. Kumar, R. S. Rao, K.Nagaiah


158 InBr3/Cu(OTf)2-Catalyzed C-alkylation of pyrrole and indoles with a-diazocarbonyl compounds

J. S. Yadav, B. V. Subba Reddy, G. Satheesh


157 LiBF4-A mild and novel reagent for O-H insertion reactions of a-diazoketones

J.S. Yadav, B. V. Subba Reddy, P. Vishnumurthy


156 InCl3-Catalyzed [3 +2] cycloaddition reactions: a facile synthesis of trans-dihydro benzofurans & substituted cyclobutanes

J.S. Yadav, B. V. Subba Reddy, G. Kondaji


155 Bi(OTf)3-Catalyzed allylation of quinones with allyltrimethylsilane



154 InCl3-immobilized in ionic liquids: a novel and recyclable catalytic system for tetrahydro pyranylation of alcohols

J. S. Yadav, B. V. Subba Reddy, D. Gnaneshwar

New Journal of Chemistry 2003, 27, 202.

153 Lewis acidic chloroaluminate ionic liquids: A novel catalyst and reaction media for the synthesis of 4-halopyrans

J. S. Yadav, B. V. Subba Reddy, M. Sridhar Reddy, N. Niranjan

Eur. J. Org. Chem. 2003, 1779.


55

152 LiClO4 or LiOTf- accelerated 1,3-dipolar cycloaddition reactions: A facile synthesis of cis-fused chromano [4,3-c] isoxazoles

J. S. Yadav, B. V. Subba Reddy, D. N. Swamy, K. Narsimulu, A. C. Kunwar

Terahedron Lett. 2003, 43, 3697.

151 Three-component one-pot synthesis of a-hydroxy phosphonates in ionic liquids

J.S.Yadav, B. V. Subba Reddy, P. Sreedhar

Adv. Syn. & Catalysis, 2003, 345, 564.

150 [Bmim]BF4 ionic liquid: A novel and recyclable reaction media for the synthesis of homoallylic amines

J. S. Yadav, B. V. Subba Reddy, A. Krishnam Raju


149 LiClO4-Catalyzed C-alkylation of pyrrole and indoles with aziridines and epoxides


J. Chem. Res. 2003, 78.

148 Ultrasound-accelerated synthesis of chiral allylic alcohols promoted by Indium metal


Tetrahedron, 2003, 59, 5333.

147 InBr3-Catalyzed sulfonation of indoles: A facile synthesis of 3-sulfonyl indoles

J.S. Yadav, B. V. Subba Reddy, A.D. Krishna, T. Swamy


146 InBr3: A novel and highly efficient reagent for the conversion of oxiranes to thiiranes

J.S.Yadav,B. V. Subba Reddy, Gakul Baishya

Synlett, 2003, 396.

145 Microwave-assisted rapid synthesis of neurotransmitter release enhancer Linopiridine and its new analogues

J.S.Yadav, B. V. Subba Reddy Synth. Commun. 2003, 33, 3115.

144 Unprecedented InCl3-catalyzed formation of cis-fused perhydrofuro [2,3-b] oxepines

J. S. Yadav, B. V. Subba Reddy, G. Satheesh, A.Prabhakar, A. C. Kunwar


143 [Bmim]PF6 ionic liquid as novel and recyclable reaction media for aromatic amination

J.S.Yadav, B. V. Subba Reddy, A.K. Basak, A.V.Narsaiah,



56

142 [Bmim]PF6: A novel and recyclable ionic liquid for the conversion of oxiranes to thiiranes in aqueous media

J.S. Yadav, B. V. Subba Reddy,Ch. Srinivas Reddy, K. Rajasekhar

J. Org. Chem. 2003, 68, 2525.

141 A novel approach for the synthesis of dipyrrolyl alkanols and dipyrrolyl alkyl amines

J.S.Yadav, B. V. Subba Reddy, P.S.R. Reddy, K.S.Reddy, P.N. Reddy

Synlett, 2003, 417.

140 Efficient and eco-friendly process for the synthesis of bis-indolylmethanes using ionic liquids

J. S. Yadav, B. V. Subba Reddy, S.Sunitha


139 CAN: a novel reagent for the synthesis of homoallyl alcohols

J. S. Yadav, B. V. Subba Reddy, A.D. Krishna, K. Sadasiv, J. Chary


138 Molecular iodine-catalyzed highly efficient and stereoselective synthesis of sugar acetylenes

J. S. Yadav, B. V. Subba Reddy, C.V. Rao, M.Sridhar Reddy


137 Three-component coupling reactions in ionic liquids: An improved protocol for the synthesis of 1,4-dihydro pyridines

J.S.Yadav, B. V. Subba Reddy, A.K. Basak, A.V. Narsaiah

Green Chemistry, 2003, 60.

136 [Bmim] BF4 ionic liquid: A novel reaction media for the synthesis of b-aminoalcohols

J.S.Yadav, B. V. Subba Reddy, A. K. Basak, A.V. Narsaiah


135 Sc(OTf)3 –catalyzed thio-glycosidation of D-glycals

J. S. Yadav, B. V. Subba Reddy, V. Geetha

Synth. Commun. 2003, 33, 717.

134 Room temperature ionic liquids promoted 3CC reactions: A facile synthesis of cis-isoquinolonic acids

J.S. Yadav, B. V. Subba Reddy, K. Saritha Raj

Tetrahedron, 2003, 59, 1805.


57

133 Aza-Diels-Alder reactions in ionic liquids: A facile synthesis of pyrano- and furanoquinolines

J. S.Yadav, B. V. Subba Reddy, J.S.S. Reddy, R.Srinivas Rao.

Tetrahedron, 2003, 59, 1599.

132 Three-component coupling reactions in ionic liquids: A facile synthesis of a-aminonitriles

J. S. Yadav, B. V. Subba Reddy, B. Eashwaraiah, M. Srinivas, P.Vishnumurthy

New J. Chemistry, 2003, 462.

131 InBr3 in ionic liquids: A novel and recyclable catalytic system for the synthesis of 1,3-dioxanes



130 Iodine as novel reagent for the 1,2-addition of trimethylsilyl cyanide to a,b-unsaturated ketones

J.S.Yadav, B. V. Subba Reddy, M. S. Reddy, A.R.Prasad

Tetrahedron, Lett. 2002, 43, 9703.

129 Amberlyst-15Ò: A novel and recyclable reagent for the synthesis of 1,5-benzo diazepines in ionic liquids

J.S. Yadav, B. V. Subba Reddy, B. Eshwaraiah, K. Anuradha

Green Chemistry, 2002, 4, 592.

128 Dy(OTf)3-immobilized in ionic liquids: A novel and recyclable reaction media for the synthesis of 2,3-unsaturated glycopyranosides

J.S.Yadav, B. V. Subba Reddy, J.S.S Reddy.

J. C. S. Perkin Trans 1, 2002, 2390.

127 Zinc-mediated acylation and sulfonation of pyrrole and its derivatives

J.S.Yadav, B. V. Subba Reddy, G. Kondaji, R. S. Rao, S. P. Kumar


126 1,4-Conjugate addition of allyltrimethylsilane to a,b-unsaturated ketones

J. S. Yadav, B. V. Subba Reddy, K. Sadasiv, G. Satheesh


125 Montmorillonite KSF clay catalyzed three component coupling reactions: A facile synthesis of homoallylic amines

J.S. Yadav, B. V. Subba Reddy, A. K. Raju, D. Gnaneshwar



58

124 Sc(OTf)3-immobilized in ionic liquids: A novel and recyclable catalytic system for hetero-Diels-Alder reaction

J.S.Yadav, B. V. Subba Reddy, U. Gayatri, A.R.Prasad


123 LiClO4-Catalyzed regioselective ring opening of aziridines with sodium azide and cyanide

J. S. Yadav, B. V. Subba Reddy, G. Parimala, P. Venkataram Reddy


122 An eco-friendly approach for the synthesis of a-amino phosphonates

J. S. Yadav, B. V. Subba Reddy, P. Sreedhar


121 InCl3–Catalyzed highly regioselective ring opening of epoxides with thiols

J.S.Yadav, B. V. Subba Reddy, Gakul Baishya


120 InCl3-catalyzed hetero-Diels-Alder reaction: A facile synthesis of pyranoquinolines

J.S.Yadav, B. V. Subba Reddy, R.S. Rao, S. K. Kumar, A. C. Kunwar

Tetrahedron, 2002, 58, 7891.

119 CeCl3.7H2O-NaI: A novel reagent system for the synthesis of 2-deoxysugars from D-glycals

J.S.Yadav, B. V. Subba Reddy, K. B. Reddy, M. Satyanarayana


118 LiClO4-Catalyzed three component coupling reactions: A facile synthesis of homo allylic amines

J.S.Yadav, B. V. Subba Reddy, P.S.R.Reddy, M. Shesha Rao


117 InBr3-catalyzed highly regioselective ring opening of epoxides and aziridines with pyrrole

J. S. Yadav, B. V. Subba Reddy, G. Parimala

Synlett, 2002, 1143.

116 InBr3- catalyzed highly stereoselective synthesis of alkynylsugars

J.S. Yadav, B. V. Subba Reddy, A. Krishanam Raju, C.V. Rao


115 Microwave-accelerated synthesis of 4-chloro tetrahydropyrans by BiCl3

J.S. Yadav, B. V. Subba Reddy, R.Srinivas, Ch. Venugopal,T.Ramalingam

Synth. Commun. 2002, 32, 1803.

114 InBr3-Catalyzed aminolysis of aziridines: An efficient synthesis of vicinal-diamines

J.S. Yadav, B. V. Subba Reddy, K.V. Rao, K. S. Raj

Synthesis, 2002, 1061


59

113 Montmorillonite KSF clay: A novel reagent for the chemoselective hydrolysis of t-butyl esters

J.S. Yadav, B. V. Subba Reddy, K. S. Rao, K. Harikishan

Synlett, 2002, 826.

112 CeCl3.7H2O-promoted highly chemoselective hydrolysis of 1,3-oxathio- and dithioacetals

J.S. Yadav, B. V. Subba Reddy, S. Raghavendra,M. Satyanarayana


111 InCl3-Catalyzed alkylation of indoles

J. S. Yadav, B. V. Subba Reddy, S. Abraham, G. Sabitha

Synlett, 2002, 1550.

110 Sc(OTf)3 catalyzed synthesis of pyrano[3,2-b] benzopyrans from D-glycals

J. S. Yadav, B. V. Subba Reddy, L. Chandraiah, B. Jagannadh, S. K. Kumar, A. C. Kunwar


109 Microwave assisted synthesis of a,a'-bis(benzylidene)ketones in dry media

J.S. Yadav, B. V. Subba Reddy, A. Nagaraju, J.A.R.P.Sarma

Synth. Commun. 2002, 32, 893.

108 Elemental iodine as novel Lewis acid: An efficient synthesis of trans-fused pyrano [3,2-c] benzopyrans

J.S. Yadav, B. V. Subba Reddy, C. V. Rao, K.Vishweshwar Rao

J. Chem. Soc. Perkin Trans 1, 2002, 1401.

107 Sc(OTf)3-catalyzed one-pot synthesis of diaryl sulfoxides

J.S. Yadav, B. V. Subba Reddy, R.Srinivas Rao, S.P. Kumar, K. Nagaiah

Synlett, 2002, 784.

106 Montmorillonite KSF clay

catalyzed [4+2] cycloaddition reactions: A facile synthesis of pyrano- and furanoquinolines

J.S. Yadav, B. V. Subba Reddy, K.Sadasiv, P.S.R.Reddy


105 Zinc-mediated Barbier reactions of pyrrole and indoles: A new method for the alkylation of pyrrole and indoles

J.S. Yadav, B. V. Subba Reddy, P. Muralikrishna Reddy, Ch. Srinivas



60

104 Montmorillonite KSF clay

catalyzed cleavage of aziridines with alcohols

J.S. Yadav, B. V. Subba Reddy, E. Balanarsaiah, S. Raghavendra


103 LPDE-catalyzed intra-molecular[4+2] cycloaddition of aryl amines: A facile synthesis of tetrahydro-chromanoquinolines

J. S. Yadav, B. V. Subba Reddy, C. V. Rao

Synlett, 2002, 993.

102 A facile synthesis of indeno [1,2-b] chromanes catalyzed by Sc(OTf)3

J. S. Yadav, B. V. Subba Reddy, Celine Parrisse, P. Cavalho, T.P. Rao


101 InCl3-catalyzed efficient conversion of carbonyl compounds to 1,3-dithio acetals

J.S.Yadav, B. V. Subba Reddy, S.K.Pandey

Synth. Commun. 2002, 32, 715.

100 InBr3 catalyzed Ferrier rearrangement: A facile synthesis of pseudoglycals

J. S. Yadav, B. V. Subba Reddy

Synthesis, 2002, 511

99 Microwave-assisted rapid synthesis of cytotoxic alkaloid Luotonin A



98 In(OTf)3 catalyzed ring opening of aziridines with carboxylic acids

J.S.Yadav, B. V. Subba Reddy, K.Sadasiv, K.Harikishan


97 FeCl3 catalyzed diastereo-selective the synthesis of 2H-1-benzopyrans

J.S.Yadav, B. V. Subba Reddy, V.Geetha

Synth. Commun. 2002, 32, 763.

96 An improved synthesis of pyrazolines from aryl azides and acrylic esters

J.S.Yadav, B. V. Subba Reddy, V. Geetha

Synlett, 2002, 513.

95 Sc(OTf)3 catalyzed electrophilic amination of arenes: An expeditious synthesis of arylhydrazides

J.S.Yadav, B. V. Subba Reddy, G.Veerendhar R.S. Rao, K.Nagaiah



61

94 Metal triflates catalyzed efficient synthesis of 3,4-dihydro-2H-1-benzopyrans

J.S.Yadav, B. V. Subba Reddy, M. Aruna, Ch. Venogopal, T.Ramalingam, S. K. Kumar

J. C. S. Perkin Trans 1, 2002, 165.

93 LiBF4-mediated conversion of aldehydes to gem-diacetates

J.S.Yadav, B. V. Subba Reddy, Ch. Venugopal, T. Ramalingam

Synlett, 2002, 604.

92 InCl3-catalyzed stereoselective synthesis of C-glycosyl hetero aromatics

J.S.Yadav, B. V. Subba Reddy, A.V. Ramana, N. Nirangen S. K. Kumar, A.C.Kunwar


91 Efficient and selective cleavage of t-butoxycarbonyl group from carbamates and amides by CeCl3.7H2O/NaI

J. S. Yadav, B. V. Subba Reddy, K.S. Reddy

Synlett, 2002, 468.

90 A facile synthesis of trans-fused pyrano[3,2-c]benzo pyrans catalyzed by Sc(OTf)3

J.S.Yadav, B. V. Subba Reddy, M. Aruna


89 KF-Al2O3 mediated cross-cannizzaro reaction under microwave irradiation

B. V. Subba Reddy, R.Srinivas, J.S.Yadav, T.Ramalingam

Synth. Commun. 2002, 32, 219.

88 InCl3-chemoselective conversion of aldehydes to gem-diacetates

J.S. Yadav, B. V. Subba Reddy & Ch.Srinivas

Synth. Commun. 2002, 32, 1175.

87 InCl3 Catalyzed conjugate addition of 1,3-dicarbonyl compounds to a,b-unsaturated ketones

J. S. Yadav, B. V. Subba Reddy, V. Geetha

Synth. Commun. 2002, 32, 3519.

86 A facile and selective cleavage of prenyl esters catalyzed by CeCl3.7H2O-NaI

J. S. Yadav, B. V. Subba Reddy, C. V. Rao, P. K. Chand & A. R. Prasad

Synlett, 2002, 137.

85 Indium mediated Barbier reactions of azides: A facile synthesis of N-alkylamine derivatives

J.S.Yadav, Ch. Madhuri B. V. Subba Reddy, G.S.K.K.Reddy, & G.Sabitha

Synth. Commun. 2002, 32, 2771.


62

84 InCl3 catalyzed regioselective opening of aziridines with heteroaromatics

J.S.Yadav, B. V. Subba Reddy, S. Abraham & G. Sabitha


83 InCl3-catalyzed regioselective ring opening of aziridines with TMS azide

J.S. Yadav, B. V. Subba Reddy, G. M. Kumar, Ch.V.S.R.Murthy

Synth. Commun. 2002, 32, 1797.

82 Yb(OTf)3-catalyzed facile conversion of ketoximes to amides

J. S. Yadav, B. V. Subba Reddy, A. V. Madavi, Y. S. S. Ganesh

J. Chem. Res. 2002, 236.

81 LiClO4-catalyzed regioselective ring opening of aziridines with aryl amines

J. S. Yadav, B. V. Subba Reddy, B. Jyothirmai, M. S. R. Murthy

Synlett, 2002, 53.

80 Indium mediated facile cleavage of t-butoxycarbonyl group from di-t-butylimido dicarbonates

J. S. Yadav, B. V. Subba Reddy, K. S. Reddy, K. Bhaskar Reddy


79

Indium mediated efficient conversion of 2-iodomethyl aziridine to chiral allylic amines

J. S. Yadav, A. Bandyopadhyay, B. V. Subba Reddy

Synlett, 2001, 1608.

78 First examples of C-arylation of aziridines catalyzed by indium triflate

J.S. Yadav, B. V. Subba Reddy, R. S. Rao, G.Veerendhar, K. Nagaiah


77 Ultrasound accelerated synthesis of 3,4-dihydro pyrimidinones by ceric ammonium nitrate

J.S. Yadav, B. V. Subba Reddy, K.B. Reddy, K. S. Raj, A.R.Prasad

J. C. S. Perkin Trans 1, 2001, 1939.

76 Sc(OTf)3 catalyzed 1,3-dipolar cycloaddition of aziridines with alkenes

J.S.Yadav, B. V. Subba Reddy, S.K.Pandey, P. Srihari I. Pratap.


75 Addition of pyrroles to electron deficient olefins employing InCl3

J.S. Yadav, Sunny A, B. V. Subba Reddy, G. Sabitha



63

74 InCl3–SiO2 catalyzed electrophilic amination of arenes: A facile and rapid synthesis of aryl hydrazides

J.S. Yadav, B. V. Subba Reddy, Ch. Madan, G. M. Kumar

Synlett, 2001, 1781.

73 ZrCl4-catalyzedefficient synthesis of a-aminophosphonates

J.S. Yadav, B. V. Subba Reddy, K.Saritha Raj & K.Bhaskar Reddy


72 LiBF4-catalyzed formation of fused pyrano- and furanobenzopyrans

J.S. Yadav, B. V. Subba Reddy, Ch. Madhuri, G. Sabitha, B. Jagannadh, S. K.Kumar A.C. Kunwar


71 InCl3-Catalyzed conjugate addition of indoles with electron deficient olefins

J.S.Yadav, S.Abraham, B. V. Subba Reddy & G.Sabitha


70 Indium mediated facile synthesis of chiral allylic amines.

J. S. Yadav, A.Bandyopadhyay & B. V. Subba Reddy


69 InX3 mediated regioselective ring opening of aziridines

J.S. Yadav, B. V. Subba Reddy & G.Mahesh Kumar

Synlett 2001, 1417.

68 Iodine-catalyzed stereoselective synthesis of allyl glycosides, glycosyl cyanides and glycosyl azides

J.S. Yadav, B. V. Subba Reddy, C.V. Rao, P.K.Chand & A.R.Prasad

Synlett 2001, 1638.

67 A facile and chemoselective cleavage of trityl ethers by InBr3

J.S. Yadav, B. V. Subba Reddy, R.Srinivas, A. Maiti

J. Chem. Res. 2001, 528.

66 Montmorillonite KSF clay catalyzed stereoselective syntheses of (E)- and (Z)-allyl iodides and bromides

J.S. Yadav, B. V. Subba Reddy & Ch.Madan

New J. Chemistry, 2001, 1114.

65 Sc(OTf)3-catalyzed C-glycosidation of glycals: A facile synthesis of allyl glycosides, glycosyl cyanides and glycosyl azides

J.S. Yadav, B. V. Subba Reddy, P.K.Chand



64

64 LiBF4 catalyzed imino-Diels-Alder reaction: A facile synthesis of pyrano and furoquinolines

J.S.Yadav, B. V. Subba Reddy, Ch.Madhuri, G.Sabitha


63 Sc(OTf)3 catalyzed allylation of acetals and gem-diacetates: A facile synthesis ofhomoallyl ethers and acetates

J. S. Yadav, B. V. Subba Reddy, P. Srihari

Synlett, 2001, 673.

62 Sc(OTf)3 catalyzed diastereo-selective synthesis of 4-amino-2H-1- benzopyrans

J.S.Yadav, B. V. Subba Reddy, K.C.Sekar & V.Geetha


61 Microwave assisted efficient one-pot synthesis of nitriles in dry media

J.S.Yadav, B. V. Subba Reddy, Ch.Madan

J. Chem. Res. 2001, 190.

60 Montmorillonite KSF clay catalyzed one-pot synthesis of a-amino phosphonates

J.S.Yadav, B. V. Subba Reddy, Ch.Madan

Synlett, 2001, 1131.

59 LiClO4-catalyzed one pot synthesis of pyrimidinones: An improved protocol for Biginelli reaction

J. S. Yadav, B. V. Subba Reddy, R. Srinivas, Ch. Venugopal, T. Ramalingam


58 Yb(OTf)3. H2O: A novel reagent for the chemoselective hydrolysis of isopropylidene acetals

J. S. Yadav, B. V. Subba Reddy, K. S. Reddy


57 LiBF4-catalyzed C-glycosidation of glycals: A facile synthesis of allyl glycosides

J. S. Yadav, B. V. Subba Reddy, L. Chandraiah, K. Srinivas Reddy

Carbohydrate. Res. 2001, 332, 221.

56 CAN-catalyzed O-glycosidation of glycals: A facile synthesis of 2,3-unsaturated glycosides


New J. Chemistry, 2001, 25, 538


65

55 Indium-mediated regio-selective allylation of epoxides: A facile synthesis of bis-homoallyl alcohols

J.S.Yadav. S.Anjaneyulu, Md.Ahmed, B. V. Subba Reddy

Tetrahedron Lett. 2001, 42, 2557,

54 LiBF4-catalyzed chemo-selective conversion of aldehydes to 1,3-oxathio-acetals and 1,3-dithianes


Synlett, 2001, 238.

53 Ultrasound promoted deoxygenation of sulphoxides by Sm-NH4Cl

J.S.Yadav, B. V. Subba Reddy, Ch.Srinivas, P.Srihari

Synlett, 2001, 854.

52 LiClO4-catalyzed reactions of indoles: A facile synthesis of bis-indolylmethanes

J.S.Yadav, B. V. Subba Reddy, Ch.V.S.R.Murthy, G. M. Kumar,


51 LiClO4-catalyzed aza-Diels-Alder reaction: A facile synthesis of pyrano, indeno quinolines, phenonthredinones

J.S.Yadav, B. V. Subba Reddy, R.Srinivas, Ch.Madhuri &T.Ramalingam

Synlett, 2001, 240.

50 InCl3-catalyzed allylation of gem-diacetates: A facile synthesis of homoallyl acetates

J.S.Yadav, B. V. Subba Reddy, Ch.Madhuri, G.Sabitha


49 Amberlyst-15 catalyzed novel synthesis of tetrahydro-pyranols

J.S. Yadav, B. V. Subba Reddy, K.Chandrasekhar, D.Gunasekar


48 A facile cleavage of N,N-dimethyl hydrazones by CeCl37H2O /SiO2

J.S.Yadav, B. V. Subba Reddy, M.Sashikumar Reddy, G.Sabitha

Synlett. 2001, 1134.

47 Unprecendented synthesis of Hantzsch 1,4-dihydropyridines under Biginelli reaction conditions

J.S.Yadav, B. V. Subba Reddy, P. T. Reddy

Synth. Commun. 2001, 31, 425.

46 Montmorillonite KSF clay catalyzed Prins-type cyclization reaction

J.S.Yadav, B. V. Subba Reddy, G.M. kumar, Ch.V.S. R. Murthy



66

45

A mild and efficient cleavage of gem-diacetates to aldehydes by CBr4

T. Ramalingam, R. Srinivas, B. V. Subba Reddy,J. S. Yadav

Synth. Commun. 2001, 31, 1091.

44 BiCl3-catalyzed aza-Diels-Alder reaction

B. V. Subba Reddy, R. Srinivas, J. S. Yadav, T. Ramalingam

Synth. Commun. 2001, 31, 1075.

43 Microwave-assisted efficient synthesis of dihydro -pyrimidines improved high yielding protocol for the Biginelli reaction

J. S. Yadav, B. V. Subba Reddy, E. J. Reddy, T.Ramalingam

J. Chem. Res. 2000, 354.

42 A new and efficient synthesis of 2,2-disubstituted 3,4-dihydro-2H-1-benzopyrans

J. S. Yadav, B. V. Subba Reddy,S. Riaz Hashim

J. C. S. Perkin Trans 1, 2000, 3082.

41 Sc(OTf)3-catalyzed Ferrier rearrangement: A facile synthesis of 2,3-unsaturated glycopyranosides

J. S. Yadav, B. V. Subba Reddy, Ch. V. S. R. Murthy, G. Mahesh kumar

Synlett, 2000, 1450.

40 Indium mediated reduction of b-nitrostyrenes to oximes in aqueous media

J. S. Yadav, B. V. Subba Reddy, R. Srinivas, T. Ramalingam

Synlett, 2000, 1447.

39 Sc(OTf)3-catalyzed formation of 2,4-dimethoxy-2-methyl-3, 4-dihydro-2H-1-benzopyrans

J. S. Yadav, B. V. Subba Reddy, T. Prabhakar Rao


38 Selective acylation of aliphatic alcohols in the presence of phenolic hydroxyl groups

G. Sabitha, B. V. Subba Reddy, G. S. K. K. Reddy J. S. Yadav

New J. Chemistry, 2000, 24, 63.

37 A mild and selective cleavage of t-butyldimethylsilyl ethers by InCl3

J. S. Yadav, B. V. Subba Reddy, Ch. Madan


36 A mild and selective cleavage of trityl ethers by CBr4- MeOH


Carbohydrate Res. 2000, 329, 885.

35 A mild and selective cleavage of trityl ethers by CeCl3.7H2O

J.S.Yadav, B.V.Subba Reddy

Synlett. 2000, 1275.

34 Microwave-assisted rapid Claisen rearrangement on solid phase

H .M. S. Kumar, S. Anjaneyulu, B. V. Subba Reddy, J. S. Yadav

Synlett. 2000, 1129.


67

33 Indium-mediated efficient conversion of azides to carbamates

J. S. Yadav, B. V. Subba Reddy, G. S. K. K. Reddy


32 Aromatization of Hantzch 1,4-dihydropyridines with I2/MeOH

J. S. Yadav, B. V. Subba Reddy, G. Sabitha, G. S. K. K. Reddy


31 A mild and chemo selective dealkylation of alkyl aryl ethers by CeCl3.7H2O /NaI

J. S. Yadav, B. V. Subba Reddy, Ch. Madan, S. Riaz Hashim


30 Solvent-free conversion of N,N-dimethyl hydrazones to nitriles under microwave irradiation

T. Ramalingam, B. V. Subba Reddy, R. Srinivas, J. S. Yadav

Synth. Commun. 2000, 30, 4507.

29 An efficient and selective conversion of hydrazides to esters and acids

R.Srinivas, B. V. Subba Reddy, J. S. Yadav, T. Ramalingam

J. Chem. Res. 2000, 376.

28 NaHSO4-SiO2 catalyzed chemo selective acetaliza-tion of aldehydes under microwave irradiation

J. S.Yadav, B. V. Subba Reddy, R. Srinivas, T. Ramalingam

Synlett, 2000, 701.

27 Microwave assisted efficient synthesis of N-arylamines in dry media


Green Chemistry, 2000, 2, 115.

26 CsF-Al2O3 mediated rapid condensation of phenols with aryl halides



25 A mild and efficient cleavage of p-methoxybenzyl ethers by CBr4



24 Indium mediated allylation of gem-diacetates

J. S. Yadav, B. V. Subba Reddy, G. S. Kirankumar Reddy


23 ZnCl2 montmorillonite catalyzed 3-aza-Cope rearrangement under microwave irradiation

J. S. Yadav, B. V. Subba Reddy, M. A. Rasheed, H. M. S. Kumar

Synlett, 2000, 487.


68

22 Indium-mediated

deoxygenation of amine-N-oxides in aqueous media

J. S. Yadav, B. V. Subba Reddy, M. Muralidhar Reddy


21 SiO2-catalyzed preparation of cinnamic acids under microwave irradiation

H. M. S. Kumar, B. V. Subba Reddy, P. T Reddy, D. Srinivas, J. S. Yadav

Organic Prep. & Proced. Int. 2000, 32, 81.

20 Efficient and selective protection of aldehydes as gem-diacetate using LiBr

H .M. S. Kumar, B. V. Subba Reddy, P. T. Reddy, J. S. Yadav

J. Chem. Res. 2000, 86.

19 A novel and efficient approach to mono-N –alkyl aniline via addtion of Grignard reagents to aryl azides

H.M.S. Kumar, B. V. Subba Reddy, S. Anjaneyulu, J. S. Yadav


18 Microwave assisted selective cleavage of sulfonates and sulfonamides in dry media

G. Sabitha, B. V. Subba Reddy, Sunny Abraham, J. S. Yadav

Synlett, 1999, 1745.

17 Microwave-promoted synthesis of b-aminoalcohols in dry media



16 Microwave-assisted Friedlander condensation catalysed by Montmorillonite KSF clay

G. Sabitha, R. S. Babu, B. V. Subba Reddy, J. S. Yadav

Synth. Commun. 1999, 29, 4403.

15 Deprotection of sulfonamides using Me3SiI



14 Iodine-Catalyzed mild and efficient tetrahydropyranylation /depyranylation of alcohols

H. M. S. Kumar, B. V. Subba Reddy, E.J. Reddy, J.S. Yadav


13 LiCl Catalyzed acetylations of alcohols, thiols, phenols and amines

G. Sabitha, B. V. Subba Reddy, R. Srividya, J. S. Yadav

Synth. Commun. 1999, 29, 2311.


69

12 SiO2-Catalyzed expedient syn-thesis of (E)-3-alkenoic acids in dry media

H. M. S. Kumar, B. V. Subba Reddy, E. J. Reddy, J. S. Yadav


11 Montmorillonite KSF catalyzed selective amidation of alcohols with nitriles in dry media

H. M. S. Kumar, B. V. Subba Reddy, S. Anjaneyulu, E. J Reddy, J. S. Yadav


10 Microwave assisted eco-friendly synthesis of 2-alkylated hydroquinones in dry media

H. M. S. Kumar, B. V. Subba Reddy, E. J. Reddy, J. S. Yadav


9 Conjugate addition of an allyl zinc reagent to b-nitrostyrenes

H.M.S. Kumar, B. V. Subba Reddy, P.T.Reddy, J. S. Yadav


8 Zinc-mediated allylation of azides: A novel method for the high yield preparation of N-allyl amines

H. M. S. Kumar, B. V. Subba Reddy, S Anjaneyulu, J. S. Yadav

Synlett, 1999, 551.

7 Efficient one pot preparation of nitriles from aldehydes using N-methyl pyrrolidone

H. M. S. Kumar, B. V. Subba Reddy, P. T. Reddy, J. S. Yadav


6 Non-solvent reaction: NH4OAc catalysed highly convenient preparation of trans-cinnamic acids

H. M. S. Kumar, B. V. Subba Reddy, S. Anjaneyulu, J. S. Yadav

Synth. Commun. 1998, 28, 3811.

5 TaCl5-SiO2 Catalyzed Prins reaction: Comparative study of conventional heating vs. microwave irradiation

S. Chandrasekhar, B. V. Subba Reddy

Synlett, 1998, 851.

4 An expedient and highly selective conversion of alcohols to Azides using NaN3/BF3.Et2O System

H. M. S. Kumar, B. V. Subba Reddy, S. Anjaneyulu, J. S. Yadav



70

3 LiCl-Catalyzed Knoevenagel condensation: Comparative study of conventional method as Microwave irradiation

G. Sabitha, B. V. Subba Reddy, R.S. Babu, J. S. Yadav


2 SiO2-Catalyzed Henry reaction: Microwave assisted preparation of 2-nitroalkanols in dry media

H. M. S. Kumar B. V. Subba Reddy, J. S. Yadav


1 Montmorillonite KSF Clay catalyzed highly selective O-alkylation of primary alcohols with orthoesters

H. M. S. Kumar, B. V. Subba Reddy, P. K. Mohanty, J. S. Yadav


ϮThe papers from S.No. 243, 244, 245, 246, 251, 252 correspond to the postdoctoral research work with Prof E J Corey, from Harvard Univesrity. ϮThe papers from S.No. 399, 404, 439, 443, 445, 446, 449, 465, 517 and 618 correspond to the collaboration with Prof Ajayan Vinu, from Japan. ϮThe papers from S.No. 406, 416, 424, 430, 470, 484, 499, 508, 511 and 589 correspond to the collaboration with Prof Rene Gree, from France.

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