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accountIntramolecular Enolate Alkylation: From Steroids through Cladiellins to IsolauralleneIntramolecular Enolate AlkylationsDeukjoon KimCollege of Pharmacy, Seoul National University, Seoul 151-742, Republic of KoreaFax +82(2)8880649; E-mail: [email protected]: 20.08.2013; Accepted after revision: 24.09.2013On the eve of my retirement, it is my great pleasure to dedicate this account to Professors Steven Weinreb and Gilbert Stork for theirinsightful tutelage and inspiration throughout my career.

Abstract: This account of the author’s contributions over his careerattempts to sketch out a research arc that stretches all the way fromvery simple beginnings, taking inspiration from the steroidal trans-hydrindane problem, to the development of a general strategy forthe stereoselective construction of cycloalkanecarboxylates via afolding and allylic strain controlled intramolecular ester enolate al-kylation, with applications thereof to the total syntheses of naturalproducts of modest complexity. Examination of the correspondingSN2′ version of this methodology led to a serendipitous discoverythat ultimately produced the olefin geometry dependent intramolec-ular amide enolate alkylation. Applications and extensions of thismethodology have enabled completely substrate-controlled asym-metric total syntheses of diverse medium-ring oxacyclic marine nat-ural products, and a fortuitous discovery along the way involving anorganoselenium-based method led to an intriguing biomimetic syn-thesis of Laurencia metabolites. Observations are made regardingaspects of a research career in retrospect.

1 Introduction2 Intramolecular SN2 Enolate Alkylation3 Intramolecular SN2′ Enolate Alkylation4 Synthesis of α,α′-cis-Disubstituted Medium-Ring Oxa-

cyclic Marine Natural Products5 Synthesis of α,α′-trans-Disubstituted Medium-Ring Oxa-

cyclic Marine Natural Products6 General Synthetic Plan for Dioxabicyclic Bromoallene

Marine Natural Products Having either a 2,10-Dioxabi-cyclo[7.3.0]dodecene or 2,9-Dioxabicyclo[6.3.0]undeceneSkeleton

7 ConclusionKey words: intramolecular enolate alkylation, natural products,substrate-controlled synthesis, medium-ring ethers, ring-closingmetathesis

1 Introduction

Owing to their physiological activities and esthetic molec-ular architecture, steroids, such as cortisone (1) (Scheme1), have played a very important role in the developmentof new synthetic methodologies, notably exemplified byGilbert Stork’s work in this area. In particular, the thermo-dynamically less stable trans-fused CD ring system (theso-called trans-hydrindane) found in most steroids hasserved as an attractive and challenging target for syntheticorganic chemists.

Predictably, Stork’s predilection for important synthesisproblems influenced me when I started my independentresearch in the early 1980s at the College of Pharmacy,Seoul National University, and I embarked on a novel ste-reoselective construction of the trans-hydrindane system.I envisioned that the intramolecular ester enolate alkyla-tion (IEEA) of tosylate 2 might produce cis-1,2-dialkylcy-clohexanecarboxylate 3 in a stereoselective manner withthe creation of a quaternary carbon center, probablythrough ‘H-eclipsed’ transition state geometry A, as ratio-nalized on basis of the allylic strain concept. This producthardly looks like a trans-hydrindane precursor; the n-bu-tyl side chain does not have any functionality necessaryfor forming the five-membered D ring, not to mention thecyclohexane C ring having nothing from which to growout the A and B rings.

Scheme 1 Approach to steroidal trans-hydrindanes via intramolecu-lar ester enolate alkylation

Resources in the laboratory were sparse at the time, andthe only organometallic reagent we had was a bottle of n-butyllithium (n-BuLi); this we used to introduce the n-bu-tyl side chain and to generate lithium diisopropylamide(LDA). When I visited Professor Eiichi Nakamura at theTokyo Institute of Technology (now at the University ofTokyo), he arranged for me to meet Professor Jiro Tsuji.While visiting his office, Tsuji told me, “Please take anyequipment or reagent that you need from my laboratoriesback with you”, which overwhelmed and thrilled me. Itook one of many shiny brand-new Schlenk flasks in his

CO2Et

H

CO2Et

H

TsO

LiO

EtO HOTs

LDA, THF

–78 °C[98:2]

cortisone (1)O

O

OH

O

OH

H H

C D

A

2 3

SYNLETT 2014, 25, 0033–0057Advanced online publication: 12.11.20130 9 3 6 - 5 2 1 4 1 4 3 7 - 2 0 9 6DOI: 10.1055/s-0033-1340050; Art ID: ST-2013-A0802-A© Georg Thieme Verlag Stuttgart · New York

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34 D. Kim ACCOUNT

Synlett 2014, 25, 33–57 © Georg Thieme Verlag Stuttgart · New York

laboratories back home, and used that memorable glass-ware to generate the LDA solution.Our work was published in Tetrahedron Letters in 1986and became the first publication of my independent ca-reer.1 Apparently, the reviewers recognized the syntheticpotential of our IEEA methodology despite the drawbacksdiscussed above. I had never had any doubts that the IEEAwould work and could be developed into a viable method-ology. That was because when I showed it to him on theblackboard in his office, Gilbert Stork told me it was agood idea.

2 Intramolecular SN2 Enolate Alkylation

Since our early work, we have examined the scope of ourintramolecular enolate alkylation methodology in termsof ring size and other parameters within the context of nat-ural product total synthesis, with particular emphasis onstereo-, regio-, and chemoselectivity. This effort has beenwell rewarded.By the following year of our initial work, we had accom-plished an efficient synthesis of geijerone (4) based on anortho ester Claisen rearrangement/IEEA strategy (Scheme2).2 It is plain to see from the enhanced sophistication inthe synthetic intermediate that by that time the laboratorywas better funded and we had more chemicals and equip-ment.Our manuscript describing this work was submitted toTetrahedron Letters, but was rejected on the grounds thatit represented merely an extension of our previously re-ported work – I had no convincing counterargument tothat! We then submitted the same manuscript to the Jour-nal of Organic Chemistry as a communication. I cannotrecall my rationale for such a move, but in the event it wasaccepted with minor revision.A complicating factor was that I had already applied for agrant with the ‘proposed’ synthesis of geijerone, since Ianticipated the manuscript would be rejected again. Atthat time, it was the customary grantsmanship strategy to

write up a proposal covering work that had been more orless already completed. That way, one could publish theresults soon after the grant was approved, and then start anew project with the funding. However, if the communi-cation was published before a decision was reached on mygrant proposal, I reasoned that I might need to explain theembarrassing scenario.I called the late Professor Werner Herz, my editor, withthe peculiar request that he delay the publication of ourcommunication. I might add that international telephonecalls at that time were still very expensive. He told me, “Ifyou don’t mind my saying this, the whole thing sounds abit silly to me. Everyone else is calling me to facilitatepublication, not to delay it. It is supposed to be a commu-nication for rapid publication.”Around that time, the late Professor Barton visited Seoulfor an international conference. Most of the Koreanspeakers did not have much to talk about on their indepen-dent research, and we were allocated about 15 minuteseach. After my talk, Professor Barton told me, “You spokevery well, but you should synthesize something that is bi-ologically active.” I replied, “If I do that, it is highly likelythat I will get scooped every time.” He told me then,

Scheme 2 Intramolecular ester enolate alkylation in the synthesis ofgeijerone (4)

geijerone (4)

OH

CO2Et

H

CO2Et

H

TsO KHMDSTHF

74%[>96:4]

S

S

S

S

KO

EtOTsO H

S

S

Biographical Sketch█

Deukjoon Kim was born in1948 in Pusan, Korea, andgraduated from the Collegeof Pharmacy, Seoul Nation-al University, in 1970. Hereceived his doctoral degreein chemistry from the De-partment of Chemistry,Fordham University, USA,under the mentorship ofProfessor Steven M. Wein-reb, and carried out postdoc-toral work under the

guidance of Professor Gil-bert Stork at the Departmentof Chemistry, ColumbiaUniversity. He joined thefaculty of the College ofPharmacy, Seoul NationalUniversity, in 1983 and re-tired from there on August31, 2013. His research inter-ests are focused on the totalsynthesis of structurallycomplex natural products,especially those having bio-

logical activity. He waselected to the Korean Acad-emy of Science and Tech-nology in 1999, was aninvited lecturer at the 2008Natural Products GordonResearch Conference(GRC), and was the recipi-ent of the 2011 KoreanAcademy of Science andTechnology Award.

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ACCOUNT Intramolecular Enolate Alkylations 35

© Georg Thieme Verlag Stuttgart · New York Synlett 2014, 25, 33–57

“Even so, you should try to synthesize a biologically ac-tive molecule.”I followed his advice, and the first synthetic target havingboth decent structural complexity and potent biologicalactivity which captured my attention at this early stage ofmy career was (–)-fumagillol (5), a saponification productof the antiangiogenic fumagillin. We were intrigued bythe possibility that an intramolecular glycolate enolate al-kylation, as summarized in Scheme 3 (6 → 7, the ratiogiven in square brackets is the ratio of isomeric products),might be utilized to help install the spirocyclic epoxidefunctionality in fumagillol in a stereoselective fashion.One of the students involved in this first asymmetric totalsynthesis of fumagillol3 continued working in this area ata pharmaceutical company, and has recently developed asemisynthetic analogue from fermented fumagillol whichis undergoing clinical trials. It seems that in the end, I ac-complished something that the late Professor Bartonwould consider useful, albeit in a vicarious manner.

Scheme 3 First asymmetric total synthesis of fumagillol (5) via in-tramolecular glycolate enolate alkylation

We successfully applied our folding and allylic strain con-trolled IEEA methodology to the total synthesis of naturalproducts that possess a cyclopentane nucleus with a di-verse substitution pattern. Furthermore, our synthesis ofoppositol (8), outlined in Scheme 4, touched on a differentperspective in the sense that the IEEA strategy (9 → 10)was elaborated to establish the relative stereochemistry ofthe three contiguous stereogenic centers in the cyclopen-tane nucleus of the natural product in a single operation.4This was accomplished using a doubly diastereodifferen-tiating, folding and allylic strain controlled IEEA in whichthe preferred H-eclipsed ester enolate B with its bulkyside chain appendage in an equatorial position distin-guishes the two homomorphic diastereotopic bromoethylgroups.At a research meeting during my time at Columbia, Gil-bert Stork mentioned in passing an example in which heemployed a doubly diastereodifferentiating process whichwas disclosed in a US patent in the late 1950s (!).5 This

awesome chemistry done at such an early date made adeep impression on me, and I have no doubt it was the in-spiration for our key step.In 1984, Professor Takashi Tokoroyama in Japan intro-duced the terminology ‘folding strain control’ to elaborateon the diastereoselectivity observed during intramolecularcyclization reactions,6 and our IEEA reactions are fine ex-amples of this concept. In fact, Tokoroyama systematical-ly investigated the diastereoselectivity of our IEEAmethodology for the construction of cyclohexanecarbox-ylates with additional substituents at various positions inthe chain in connection with the concept of folding straincontrol, and in 1996 he and Kusaka published a full paperentitled Folding Strain Stereocontrol in CyclohexaneRing Formation by Means of an Intramolecular EsterEnolate Alkylation Reaction.7

I must confess that in the past, I would deliberately de-scribe our examples of intramolecular enolate alkylationsas folding and allylic strain controlled in part for a nonsci-entific reason: it was a shrewd gamble that our manuscriptmight go to Tokoroyama for review! To the best of myknowledge, I was the only one besides him who activelyused the phrase ‘folding strain controlled’. When I gave atalk at the 2nd Korea–USA Joint Symposium on OrganicChemistry in Seoul, I recall referring to such situations as‘chemopolitics’, and this seemed to strike a resonantchord with the audience, in particular among the Ameri-can delegation. Incidentally, this group included about adozen eminent organic chemists, and this had a huge im-pact on the Korean organic synthesis community, but un-fortunately the symposium was discontinued afterwardsowing to budgetary problems. The postsymposium cele-bration was a highly memorable event in true ‘GangnamStyle’, well before Psy managed to acquaint the rest of theworld with that way of life.Owing to its remarkable biological activity, grandisol (14)(Scheme 5), a sex attractant of the male boll weevil An-

(–)-fumagillol (5)

HO

MeO

O

H O

CO2Me

BnO

MeO

BnO

H

CO2Me

BnO

MeO

BnO

H

TsOKHMDS

THF

[11:1]

BnOOMe

H

OK

BnO

OMe

TsO

6 7

Scheme 4 Synthesis of oppositol (8) via doubly diastereodifferenti-ating, folding and allylic strain controlled intramolecular ester enolatealkylation

Br

HO

EtO2C

Br

O O

PMBO

BrEtO2C

Br

O O

PMBO

KO

EtO Br H

OO

Br

KHMDSTHF

oppositol (8)

9 10

B

OPMB

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36 D. Kim ACCOUNT


thonomus grandis Boheman, has served as a testingground to evaluate strategies for the stereoselective con-struction of four-membered rings, as exemplified byStork’s epoxy nitrile cyclization.8 In addition, the diaste-reomer fragranol (11) has been isolated from the roots ofArtemisia fragrans Willd. Obviously, we were interestedin whether our folding and allylic strain controlled IEEAstrategy would be viable in the case of four-memberedring synthesis.9

This study illustrated a general trend in our methodology;namely, the larger the size of the α-substituent group (R),the more inferior the stereoselectivity, as exemplified bythe isomeric ratios of 19:1 and approximately 2:1achieved for the intramolecular alkylation of an α-methyl-substituted ester (12 → 13) and the corresponding α-allyl-substituted derivative (15 → 16), respectively (Scheme5). The inferior stereoselectivity observed in the transfor-mation of allyl derivative 15 into cyclobutane 16, a step inthe potential synthesis of grandisol (14), was overcomeusing the intramolecular alkylation of a cyclic enolate – aγ-lactone enolate (17 → 18).

Scheme 5 Synthesis of grandisol (14) via intramolecular lactoneenolate alkylation

I would like to digress for a while to describe a back-ground story about our brefeldin synthesis, which waspublished in 1995.10 Under normal circumstances, Iwould not have been interested in a total synthesis ofbrefeldin A (19), simply because its cyclopentane nucleusdoes not possess a quaternary center. However, my casualcuriosity about the comparative stereoselectivity ofbranched ester enolates and linear nitrile anions in intra-molecular alkylations drew us into a study of the brefeldinproblem. An additional reason was that it became a matterof honor (vide infra)!

A literature search revealed that Kitahara and Mori hademployed the intramolecular nitrile anion alkylation (IN-AA) of nitrile 20 in their synthesis of brefeldin A, as de-picted in Scheme 6.11 Given the presence of an acidicproton in product 21, one could argue whether or not theobserved stereoselectivity (92:8) reflects a kinetic prefer-ence under the cyclization conditions (NaHMDS, ben-zene, reflux, 20 min). Despite this concern, which couldhave jeopardized the logic behind our particular compar-ative study, we proceeded to examine the stereoselectivityof the intramolecular alkylation of ester counterpart 22 ofthe Mori nitrile, thinking this would take only severalmonths. In reality, this issue occupied our attention formore than ten man years!

Scheme 6 Branched ester enolate versus linear nitrile anion alkyla-tion

After considering synthetic routes to ester 22, we decidedwe might as well pursue the synthesis of a more advancedintermediate for brefeldin A, such as Bartlett intermediate23.12 Shown in Scheme 7 is the initial retrosynthetic planI conceived, somewhat naively in retrospect, and this wasgiven to a part-time student who was doing his Ph.D.while working for a pharmaceutical company. It was pat-terned after the sequential acyclic Claisen rearrangementstrategy used in Stork’s ingenious prostaglandin synthe-sis.13

The scheme seemed straightforward, except that the sec-ondary hydroxy groups in diol 24 required differentiatingfor the sequential [3,3]-sigmatropic rearrangement. I be-lieved that this could be achieved through the preferentialintramolecular formation of a six-membered-ring mixedketal in methanol, incorporating the homoallylic hydroxygroup and thus exposing the allylic one, as depicted incompound 25 (Scheme 7).My student, who was carrying out his research work at thecompany after work hours, made dihydroxy ketone 24 inno time and next attempted the intramolecular ketal for-mation in methanol as I suggested. He called me and said,“I don’t get anything after column chromatography, al-though I saw a distinct nonpolar spot in the TLC of the re-

KO

R

EtO H

KHMDSTHF

85% [19:1] H

fragranol (11)

H

grandisol (14)

CO2Et

H

TsO CO2Et

H

OTs

OH

CO2Et

H

TsO CO2Et

H

H

O

O

H

O

O

ILiHMDS

THF

90%(18 only)

KHMDSTHF

[~2:1]

17 18

12 13

15 16

OH

CN

H

MEMO

TsOCN

H

H

MEMO

CO2Et

H

MEMO

TsOCO2Et

H

H

MEMO

NaHMDSPhH, reflux

20 min

81%[92:8]

?

OH

H

HO

OHO

(+)-brefeldin A (19)

20

22

21

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action mixture.” That gave me an anti-eureka moment (!)because I had neglected the possibility of intramolecularbicyclic ketal formation occurring from the diol function-ality in substrate 24 (Scheme 8) which nevertheless iswell-documented in the synthesis of brevicomin.14 I toldhim to evaporate the eluent at a lower temperature and hebrought me the NMR spectrum, which indicated we hadaccomplished an unintended formal synthesis of exo-brevicomin (26).

Scheme 8 Unintended formal synthesis of exo-brevicomin (26)

I had lost face, which is a grave matter to an East Asianprofessor, especially when my students thought I was sosmart after they heard I was trained in a major researchgroup in the United States! Desperate to save face by com-ing up with a superior synthesis of brefeldin A, I meticu-lously went over all the existing syntheses of this naturalproduct, including total and formal syntheses and synthet-ic approaches – more than 20 of them at the time – duringthe whole summer vacation.10b At the time, brefeldin wasa hot topic owing to its biological activity and interestingmolecular structure. The list of researchers who investi-gated this problem read like a Who’s Who of natural prod-uct synthesis chemists, and it was a tall order to come upwith another and superior synthesis.

One day, out of the blue, an idea came to mind: why notlet the chirality of the remote C-15 hydroxy group controlthe configuration of the rest of the stereogenic centers inthe molecule by a triple chirality transfer process? Veryfortunately, a synthetic plan fell into place like magic(Scheme 9). Thus, we accomplished a 12-step synthesis ofthe advanced brefeldin intermediate 28 from readily avail-able ethyl O-benzyl lactate. Chemoselective sodium boro-hydride reduction of the α-alkoxy ester in the third Claisenrearrangement product 27 in the presence of a simple esterwas instrumental in its brevity. I still feel a bit odd claim-ing this as a 12-step synthesis while invoking a diazo-methane workup twice as uncounted steps. Nevertheless,I consider this fortuitous synthesis one of the highlights ofmy entire career and a not inelegant recovery from an em-barrassing misjudgment.

3 Intramolecular SN2′ Enolate Alkylation

Meanwhile, we were intrigued by a possible alternative tothe previously described way of controlling the relativestereochemistry of three stereogenic centers in a singleoperation, i.e. different from the elaborate doubly diaste-reodifferentiating IEEA protocol. We reasoned that afolding and allylic strain controlled intramolecular SN2′enolate alkylation might offer such an alternative.15 Yearsago, when I told Gilbert Stork that I was going back to Ko-rea, he asked me whether I would have an NMR spectros-copy machine, and further mentioned that I could studySN2′ reactions even under relatively spartan conditions.Obviously, his encouragement had a significant influenceon my pursuing this avenue of inquiry.Our successful efforts along these lines are exemplified inour synthesis of elemol (29), as summarized in Scheme10.16 In this work, we established the relative stereochem-istry of all three stereogenic centers in the natural productin a single operation using a folding strain controlled in-tramolecular SN2′ ester enolate alkylation (30 → 31),which probably proceeds through chairlike double H-eclipsed transition state geometry C, as depicted inScheme 10.With the advent of the ring-closing metathesis (RCM)methodology, it was quite fulfilling to revisit the steroidaltrans-hydrindane problem by employing an intramolecu-lar SN2′ amide enolate alkylation strategy (34 → 35) andRCM. Thus, we achieved a concise, seven-step synthesisof trans-hydrindane 32 from commercially available 2-acetylcyclopentanone (33), as illustrated in Scheme 11.17

In an effort to apply our internal SN2′ strategy to alkaloidsynthesis, intramolecular SN2′ lactam enolate alkylationwas carried out on substrate (E)-37, which has an (E)-al-lylic chloride pendant moiety. Exposure of (E)-37 topotassium hexamethyldisilazide provided the desired spi-rocyclic intermediate 38 in a 43:1 isomeric ratio, and thiswas converted into isonitramine (36) in racemic form(Scheme 12).18 As in the previously described grandisol

Scheme 7 Initial retrosynthetic plan for brefeldin A (19)

CO2MeH

H

MOMOOH

CO2Me

H

MOMO

TsO

(+)-brefeldin A

HO

OH O

HO

O

sequential[3,3] rearrangement

OMe

Bartlettsynthesis

D-(–)-tartaric acid

HO2CCO2H

HO

OH

IEEAOP

23

24

25

?

19

HO

OH O 1 M HClMeOH

r.t., 3 h

(1R,5S,7R)-(+)-exo-brevicomin (26)

O

O H

H

O

O H

H

24

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38 D. Kim ACCOUNT


synthesis, the observed stereoselectivity in the case of thecyclic enolate was excellent.Encouraged by the success of the double allylic straincontrolled intramolecular SN2′ strategy, we formulated asynthetic plan for the asymmetric synthesis of (+)-isonit-ramine [(+)-36] based on a triple allylic strain controlledversion. In this example, the chirality of the 1-phenyle-thylamine moiety in substrate (E)-39 induced that of thespirocyclic quaternary carbon atom in the desired inter-mediate 40 in a 1,4-fashion with a selectivity of 6.2:1(Scheme 13).19

During our synthetic study on (+)-isonitramine, we madethe very interesting and fortuitous observation on one oc-casion of the formation of a tiny amount of compound 41

in addition to the previously mentioned 6.2:1 stereoiso-meric mixture of six-membered-ring SN2′ product 40(Scheme 14).20 The spectral data suggested an eight-mem-bered ring structure for this minor product, and very for-tunately we were able to ascertain that the startingmaterial used in that particular experiment was contami-nated with a small amount (ca. 5%) of the correspondingZ-isomer.Subsequently, we independently synthesized the isomericallylic chloride (Z)-39 and subjected it to comparable cy-clization conditions. Eight-membered ring product 41 wasformed in high yield as a single diastereomer (the spirocy-clic carbon stereochemistry was undetermined), identicalto that obtained previously (Scheme 14).

Scheme 9 Triple chirality transfer/intramolecular ester enolate alkylation strategy for brefeldin A (19)

O

H

OBnHH

OM

PMBO

OBn

OPMBO

O

HO2C

OBnOPMB

EtO2C

OBnOBn

HO

MeO2C

OBnOPMB

OBnOPMB OBnOPMB

HO2C

MOMO

OMOMO

O

OBn

H

CO2Et

MOMO

ICO2Et

H

H

MOMOOBn

OBn

H

CO2Et

MOMO

HO

ethyl O-benzyl (S)-lactateCCNA: chelation controlled nucleophilic addition

Burke one-pot reaction

DIBAL-H, CCNA

1st [3,3] rearrangement

acylation

iodination

LiHMDSTHF

0 °C, 30 min92%

IEEA28

Burke reaction

acylation

CH2N2

wet DDQ

CH2N2

H2/cat.

O

H

OPMBH

MOMOO

OBn

M

2nd [3,3] rearrangement

OBnOH

MeO2C

MOMO OBn

MOMO

MeO2C

H

CO2Et

O

EtOH

H

HMeO2C

MOMO

OBn

27

3rd [3,3] rearrangement

NaBH4

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Scheme 10 Synthesis of elemol (29) via folding and double allylicstrain controlled intramolecular SN2′ ester enolate alkylation

Scheme 11 Concise construction of steroidal trans-hydrindane 32using a folding and allylic strain controlled intramolecular SN2′ alkyl-ation/ring-closing metathesis strategy

Next, we made a large quantity of the corresponding sim-pler N-benzyl compound (Z)-37 to investigate this inter-

esting observation in detail. However, we were quitesurprised to find that this (Z)-allylic chloride, which lacksa methyl group at the benzylic position, did not produceany of the desired product under comparable conditions(Scheme 14). This was probably due to the acidity of thebenzylic hydrogens under the strong basic reaction condi-tions.As far as we are concerned, this failure because of such asubtle difference is quite significant. Had we not tried theasymmetric version of the isonitramine synthesis, wemight have never discovered the efficient methodologyfor the construction of medium-sized rings which I willdescribe from here on.

KHMDSTHF

57%[89:5:5:1]

H H OH

elemol (29)

EtO2C

H H OBOM

EtO2C

H OBOMCl

OBOM

HCl

EtO

OKH

H

C

30 31

KHMDSTHF

OCl

N

Me

Me

H

N

MeO

Me

H

N

MeO

Me

C D

OO

33commercially available

5 steps N

HCl

OKH

3435

RCM

32

71% total yield[10:1:1:1]

Scheme 12 Synthesis of racemic spirocyclic alkaloid isonitramine(36) via double allylic strain controlled intramolecular SN2′ lactamenolate alkylation

KHMDS, THF–78 °C, 1 h, then

55 °C, 0.5 h

62%[43:1]

rac-isonitramine (rac-36)

HCl

N

OK

NH

OHH

N

H

O

N

O

Cl

H

(E)-37 38

Scheme 13 Asymmetric synthesis of (+)-isonitramine [(+)-36] viatriple allylic strain controlled intramolecular SN2′ lactam enolate al-kylation

KHMDStoluene

70 °C, 4 h

70% total yield[6.2:1]

(+)-isonitramine [(+)-36]

Cl

N

OK

NH

OHH

N

H

OH

N

OH

Cl

H

H

H

(E)-39 40

Scheme 14 Accidental entrée into medium-ring cyclizations

N

O

Cl

H

N

H O

N

H O

N

H O

+

KHMDStoluene

75 °C, 3 h73%

E/Z = 95:5

N

H O

Cl

N

O

Cl

N

O

39

40

(Z)-39

41(a very small amount)

(Z)-37

41

H

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40 D. Kim ACCOUNT


4 Synthesis of α,α′-cis-Disubstituted Medium-Ring Oxacyclic Marine Natural Products

Owing to my obtuse nature, as well as our obsession withthe stereoselective creation of quaternary centers, we didnot fully appreciate the synthetic potential of the aboveserendipitous discovery for quite some time. It was notuntil medium-ring oxacyclic marine natural products be-gan to succumb to total synthesis with the advent of theRCM methodology, notably achieved by the researchgroup of Professor Michael Crimmins, that we turned ourattention to this area. We envisaged that the adaptation ofour fortuitous finding to the key step of intramolecularglycolate enolate alkylation, which we employed previ-ously in our fumagillol synthesis (see Section 2), mightoffer us a viable synthetic strategy for the construction ofmedium-ring oxacycles.Our model study to test the feasibility of this approach ledto what we term the ‘olefin geometry dependent internalalkylation’ strategy, where the geometry of the olefin con-trols the mode of cyclization, as illustrated in Scheme15.21 Thus, trans-olefin (E)-42 gave rise predominantly tosix-membered ring 43 through an SN2′ pathway as antici-pated, while cis-olefin (Z)-42 produced mainly eight-membered ring 44 via a simple SN2 reaction.

Scheme 15 Olefin geometry dependent intramolecular amide eno-late alkylation

With this encouraging result, the focus of our researchshifted to the asymmetric total synthesis of medium-ringoxacyclic marine natural products. Figure 1 illustrates thestructures of those natural products whose syntheses arecovered in this account. Some of the medium-ring oxacy-clic marine natural products possess so-called α,α′-cis sidechain appendages and others have the α,α′-trans arrange-ment. I have used the colors violet and green to indicatethe cis and trans relationships, respectively, throughoutthe rest of this account. In addition, I would like to pointout that both Z- and E-isomers are found in nature in thecase of oxonenes.Before further discussing our work, I would like to men-tion that we have pursued efficient, ‘entirely substrate-controlled’ asymmetric total synthesis wherever appropri-

ate. In connection with this, Smith and Empfield intro-duced the concept of a ‘stereochemically linear strategy’for this approach.22 To track this strategy more easily, Ihave used a black asterisk circled in yellow to indicate theorigin or source of absolute chirality, and red and blue as-terisks to denote stereocenters induced by substrate con-trol and asymmetric methods, respectively. In addition,the size of each asterisk indicates the sequence in whichthe corresponding stereocenter was introduced; the largerthe asterisk, the later it was introduced. This notation,which is used throughout the rest of this account, is illus-trated in Scheme 16 using the previously described syn-thesis of (+)-brefeldin A as an example (see Section 2).The problems we needed to address for synthesis of themedium-ring oxacyclic natural products were as follows:Firstly, one must construct the medium-ring oxacyclicskeleton while dealing with the very important problem ofcontrolling the relative stereochemistry of the two sidechain appendages, which are either α,α′-cis or α,α′-trans.Secondly, one must then deal with the elaboration of theflexible side chain, which often possesses stereogeniccenters, enynes, bromoallene moieties, etc. Finally comesthe introduction of a halogen atom with a defined stereo-chemistry, which in my opinion is the most demandingtask. It turns out that this seemingly simple synthetic op-

SN2

SN2'

(E)-42

(Z)-42

43 (six-membered)

44 (eight-membered)

OO

NMe Me

OO

NMe Me

Cl

O

N

O

Me Me

OO

NMe Me

Cl

Figure 1 Representative medium-ring oxacyclic marine naturalproducts

(R)

O

H

H

Br

H

H

OH

H

H Br(–)-isolaurallene

α,α'-cis

α,α'-trans

(S)

O

H

H

Br

H

H

OH

H

Br Hα,α'-trans

α,α'-trans

(+)-itomanallene A

O

OH

HH

Br

H

Br H

H

(S)

(+)-laurallene

α,α'-trans

α,α'-trans

O

Cl

H

H

BrH

(+)-(3E)- and (+)-(3Z)-pinnatifidenyne

(–)-cladiella-6,11-dien-3-ol

O

H

H

H

HOH

E

(+)-laurencin

(+)-pannosallene

α,α'-cis

O

Br

H

H

AcOH

α,α'-cis

(–)-ophirin B

O

H

H

H

HOAc

AcO

OAc

Z

O

OH

HH

Br

H

Br H

H

(S)

α,α'-trans

α,α'-cis

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eration often dictates the course of the entire synthesis (vi-de infra).The next portion of this account is a series of discussionson our approaches to each of the target compounds depict-ed in Figure 1, with a focus on the crucial synthetic trans-formations. Keeping in mind our self-imposedstereochemical goal and synthetic tasks, first I will discussour substrate-controlled synthesis of α,α′-cis-natural prod-ucts. I will begin with a detailed examination of our syn-thesis of (+)-laurencin, the most well-known metaboliteof this class, to give you an idea of the type of objectiveswe were pursuing.23

With the above in mind, the retrosynthetic plan for our(+)-laurencin synthesis, depicted in Scheme 17, was quitestraightforward. It involved the preparation of the internalalkylation substrate (49 → 48), its intramolecular amideenolate alkylation (IAEA) (48 → 47), elaboration of theside chain appendage (47 → 46), and bromination (46 →45), this latter step already being known.The preparation of the key internal alkylation substrate 48is shown in Scheme 18. Thus, an Evans–Crimmins asym-metric alkylation (49 → 50)24 and Burke’s one-pot reduc-tion/chelation-controlled nucleophilic addition protocol

(51 → 52)25 were utilized to establish the target com-pound’s C-12/C-13 absolute and vicinal relative stereo-chemistry. A direct, three-step sequence then afforded therequisite internal alkylation substrate 48 in reasonableoverall yield (38% for the six steps from 49).

Scheme 18 Preparation of internal alkylation substrate 48

We were very pleased to find that the application of ourIAEA to (Z)-allylic chloride 48 proceeded quite smoothlyto give the desired α,α′-cis-oxocene 47 in excellent yield(Scheme 19). The α,α′-cis relative stereochemistry ofproduct 47 was firmly established using nuclear Over-hauser effect (NOE) spectroscopic studies (Scheme 19).This high degree of regioselectivity was gratifying, al-though it is hard to craft a convincing rationale as to whyoxocene 47 was formed at the expense of the SN2′ productvia a six-membered-ring transition state. However, giventhe potential utility of this transformation, we plan furtherinvestigations into the underlying reasons for the ob-served regioselectivity (SN2 versus the SN2′ pathway) inthis IAEA reaction.It is worth mentioning that our plan hinged upon the ver-satility of the α-alkoxy-substituted N,N-dimethylamidefunctional group as illustrated with oxocene targets inScheme 20. We had elected to use a N,N-dimethylamidegroup for the internal alkylation simply because the corre-sponding ester was unsatisfactory, and at that time we didnot fully appreciate what its value would be.The addition of organometallics, such as Grignard or al-kyllithium reagents, to the α-alkoxy-substituted N,N-di-methylamide gave the corresponding ketone directly in ahighly reliable manner (Scheme 20). I imagine that thesubconscious inspiration for this process came from theWeinreb ketone synthesis,26 which proceeds via a very

Scheme 16 Substrate-controlled asymmetric synthesis and a key tothe notations used in this account

OH

H

HO

OHO

EtO2C

OBn

(+)-brefeldin A ethyl O-benzyl (S)-lactate

3 × [3,3]rearrangement

: by substrate control

: by asymmetric methods

: source of absolute chirality

the larger the asterisk, the later it was introduced

**** **

***

Scheme 17 Retrosynthetic plan for (+)-laurencin (45)

AcO

O

BrH

HH

AcO

O

OHH

HH

N

O

O

OBnH

HH

Me

MeO

OBnH

H

Cl

N

Me

OMe

ON

OO

BnOBn

I

THPO+

known

(+)-laurencin (45)

Evansalkylation

IAEA

α,α'-cis 46

4748

49

[Br]

*

O

OBnH

H

THPO

N O

ON

OO

BnOBn I

THPOOBn

H

THPOON

OBnH

THPOHO

H

O O

Bn

OBnH

THPOMeO O

Me

Me

OBnH

THPOH O

O

OBnH

H

HO

N OMe

Me

O

OBnH

H

Cl

N OMe

Me

NaHMDS[49:1]

1. DIBAL-H2. EtMgBr

[>10:1]

MeOHDMAP

BrCH2CONMe2NaH

Ph3PCCl4

PTSAEtOH

*

**

*

1312

*49

48

50

51

52

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42 D. Kim ACCOUNT


stable metal-chelated intermediate like that shown for theabove direct ketone synthesis protocol. L-Selectride re-duction of the resultant ketone is known to proceed in ahighly stereoselective fashion, rationalized by Felkin–Ahn model D.27

The existing syntheses in this area usually employ a rathercumbersome sequence, i.e. the non-stereoselective addi-tion of an organometallic species to an aldehyde, separa-tion of the mixture, then reoxidation and L-Selectridereduction. Our versatile three-step sequence, i.e. IAEA,direct ketone synthesis, and L-Selectride reduction, con-stitutes the backbone of a synthetic strategy that enabledus to achieve concise and efficient syntheses of our targetcompounds, our routes being competitive with or surpass-ing existing approaches in terms of brevity. In addition,the N,N-dimethylamide could be converted into the corre-sponding aldehyde or primary alcohol by addition of anate complex or Superhydride, respectively (Scheme 20).As I pointed out earlier, the introduction of the halogenatom in these target compounds in a stereochemicallycontrolled manner is a considerable challenge. Figure 2summarizes our rather extensive experience28a of the ha-logenation of the four possible diastereomeric oxocenylalcohols with inversion of configuration under Hooz’sconditions.28b Whatever the exact reason might be, the ha-

logenation of the α,α′-cis-syn-oxocenyl alcohol (syn withrespect to C-12/C-13 in laurencin) usually gives a satis-factory result. Halogenation of the cis-anti- and trans-syn-isomers tends to be problematic. However, the trans-anti-isomer represents the worst substrate for halogenation.Throughout this account, I will be using the ‘ease-of-ha-logenation’ rating system shown in Figure 2, where thevalence and magnitude are indicated by the plus and mi-nus signs in the parentheses.

Figure 2 Ease of the halogenation of diastereomeric oxocenyl alco-hols (involving inversion of configuration)

To complete the synthesis of (+)-laurencin (45), the ace-tonitrile anion was used as an acetaldehyde equivalent fora direct ketone synthesis (47 → 53) (Scheme 21). Stereo-and chemoselective L-Selectride reduction (53 → 54),followed by conventional steps including a stereoselec-tive Wittig reaction (55 → 56), led to the final product.In summary, an efficient 15-step total synthesis of (+)-lau-rencin (45) was accomplished in a completely substrate-controlled fashion, starting from known glycolate deriva-tive 49 as the source of absolute chirality (Scheme 22).Would you believe it if I said that Steven Weinreb editedALL my manuscripts for more than two decades saying

Scheme 19 Intramolecular amide enolate alkylation

Scheme 20 Versatility of the α-alkoxy-substituted N,N-dimethylamide functional group

R

HO

O

OBnH

HH

R

O

O

OBnH

HH

O

OBnH

H

Cl

N

Me

OMe

N

O

O

OBnH

HH

Me

Me

OO

M

MeN

RMe

O

R

ring

H

O-ring

H–

Felkin–Ahn model

syn

D

IAEA RM L-Selectride

O O

OBnH

HH

HO O

OBnH

HH

DIBAL-H/n-BuLi Superhydride

RM = organometallic reagent

O R2

HH

R1

OHH

O R2

HH

R1

OHH

O R2

HH

R1

OHH

O R2

HH

R1

OHH

1213

α,α'-cis

C-12/C-13-syn

cis-syn (+ + +) cis-anti (–)

trans-syn (–) trans-anti (– – –)

+ + + / – / – – –good to poor

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that he wanted to know what I was doing in Korea. Luckyfor him that I was not more productive! In the olden days,he would return the edited manuscript marked up by handin a red pen via air mail. Oddly enough, I have never vis-ited him at Penn State University, but I can easily imagine

him doing the ‘Weinreb Walk’ to the post office with acan of Diet Pepsi in hand.Recently, I decided to take the load off him consideringhis advancing age, and more importantly coinciding withthe departure of one of his Ph.D. students, my former mas-ter’s student, who had acted as a liaison in this new age ofelectronic communication. I do not know how else I canrepay Steve’s boundless and enthusiastic efforts as mymentor except by wishing him the very best of luck andhealth, and by taking the opportunity in writing this ac-count to acknowledge the essential beneficial effect he hashad on my career.I imagine that chemists who have read my very recent pa-pers must have noticed that my English shows sudden tre-mendous improvement. I know there are rumors floatingaround to the effect that “Kim must have a live-in English-speaking paramour”. But the truth is that destiny broughtme back together again with a labmate at Columbia, Dr.Matthew Schlecht, who is now doing chemistry withwords in a practice named Word Alchemy. My cybermateand I exchange many, many rounds of editing and discus-sion for a manuscript – incidentally, he did his doctoral re-search on enolate chemistry, so it was a natural fit.From key IAEA product 47 in the laurencin synthesis,we have developed a highly efficient, biomimetic route to(–)-laurefucin (57) via an organoselenium-mediated oxo-nium ion formation/fragmentation protocol (58 → 59), asoutlined briefly in Scheme 23.29 As you might haveguessed by now, as with much of my work, this novel or-ganoselenium-based methodology benefited from an ele-ment of serendipity.

Scheme 21 Completion of the synthesis of (+)-laurencin (45)

HO

O

OBnH

HH

HO

O

OBnH

HH

TIPS

N

O

O

OBnH

HH

Me

Me

[10:1]

AcO

O

BrH

HH

(+)-laurencin (45)

Wittig reaction

AcO

O

OHH

HH

CBr4n-Oct3P

50%

O

O

OBnH

HH

NC

NCCH2Li

HO

O

OBnH

HH

NC * ODIBAL-H

L-Selectride

***

***

cis-syn (+ + +)

47 53

54 55

56

46

Scheme 22 Summary of the synthesis of (+)-laurencin (45)

N

O

O

OBnH

HH

Me

Me

Me

NBr

O

Me

O

OBn

O

O

OBnH

HH

Cl

N

Me

OMe

+ +BrMg

NC

THPO

I

+

O

OBn

HNC

H

HOH

AcO

O

BrH

HH

ON

OO

BnOBn

*

IAEA RM L-Selectride

(+)-laurencin (45)

49

AcO

O

OHH

HH

cis-syn (+ + +)

[Br]

H

H

* ***

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44 D. Kim ACCOUNT


Taking advantage of the known natural product chemistryin the field, we further modified the organoselenium-based methodology to arrive at a one-pot tandem or-ganoselenium-mediated oxonium ion formation/silica gelpromoted fragmentation protocol. This was used toachieve the asymmetric total synthesis of Laurencia natu-ral products that have a 2,2′-bi(tetrahydrofuranyl) skele-ton.28a

Scheme 23 Organoselenium-mediated hydroxyetherification routeto (–)-laurefucin (57)

We found it intellectually amusing that we parlayed thebiogenesis-inspired strategy for C15 Laurencia aceto-genins into an asymmetric total synthesis of trilobacin(60) (Scheme 24), an annonaceous acetogenin of a com-pletely different biogenetic origin which possesses potentanticancer activity.30 It is noteworthy that an entirely sub-strate-controlled approach for this molecule did not seemto be appropriate; the blue asterisks simply twinkle in thedistance like unreachable stars, unable to communicatewith the stereochemical core.

Scheme 24 Asymmetric total synthesis of trilobacin (60) via one-pottandem organoselenium-mediated oxonium ion formation/silica gelpromoted fragmentation

We addressed an internal alkylation issue in our synthesisof (+)-(3Z)-pinnatifidenyne (61), as depicted in Scheme25. The course of the synthesis was determined by theseemingly insignificant difference between our targetcompound 61 and (+)-laurencin (45), i.e. the relative ste-reochemistry of the ring halogen atom with respect to theadjacent alkyl group.21 The chlorination of cis-anti-oxo-cenyl alcohol 62 derived using our internal alkylation wasproblematic owing to a competing elimination reaction,and it produced only a modest yield (33%) of the desiredoxocenyl chloride 63.To overcome this obstacle, we were forced to explorechanging the order of events. Although it seemed ratherrisky at the outset, we were delighted to find that the acy-clic chlorination/internal alkylation sequence proved to behighly efficient and afforded the desired oxocene 63 ingood overall yield, demonstrating the synthetic potentialof our methodology.

O

BrH

HH

HO

O

H

H

H

(–)-laurefucin (57)

O

OBr

H

H

HH

HR

H

58

O

BrH

HH

HO

HBnO

O

BrH

HH

HO

OH

H

H

59BnO

N

O

O

OBnH

HH

Me

Me

47

O

BrH

HH

PhSe

O

R

H

H

H

PhSe

[Br], RMand

trans-annularattack

H2O

10

attackby H2O

NPSPMeCNH2O

100%

+

+

L-Selectride

PhSeClSiO2

K2CO3

CH2Cl2r.t., 24 h

83%

O

O

H

H

H

H

BnO OBn

BnO n-C10H21

Cl

H

O HH

PMBOH

OBnBnO

n-C10H21

OBn4

4

O

O

H

H

H

H

HO

HO

OO

HO

trilobacin (60)

**

**

**

* *

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Scheme 25 Highlights in the asymmetric total synthesis of (+)-(3Z)-pinnatifidenyne (61)

As the final subject of our synthesis of α,α′-cis-disubsti-tuted natural products, I will describe our endeavors to-ward the asymmetric total synthesis of cladiellinditerpenes, which exhibit a wide range of biological activ-ities.31 As I mentioned earlier, both Z- and E-isomers ofthese compounds are found in nature. These complex nat-ural products possess an α,α′-cis-disubstituted nine-mem-bered ether ring and a tertiary carbinol moiety at C-3, asdepicted in Scheme 26. The relative stereochemistry ofthe C-2 and C-3 oxygen functionalities is syn.

The Crimmins group reported the elegant syntheses of(Z)-cladiellin diterpenes, such as (–)-ophirin B (64)(Scheme 26), which employed a key RCM/intramolecularDiels–Alder (IMDA) strategy.32 We developed a generalstrategy for both (Z)- and (E)-cladiellins based on anIAEA/IMDA protocol, and in this account I will focus onthe synthesis of (E)-cladiellin diterpenes, e.g. (–)-cladiella-6,11-dien-3-ol (65), for which we believe our approacheshave a distinct edge.33

As shown in Scheme 26, (Z)-C-3 tertiary (3°)/α,α′-cis-syn-oxonene (Z)-67 could be constructed efficiently byapplying our IAEA to (Z)-allylic chloride (Z)-66. Inciden-tally, the product of the Superhydride reduction of (Z)-ox-onene (Z)-67 is a known Crimmins intermediate for (–)-ophirin B (64).32 In the case of the E-isomer (E)-66, how-ever, the chemical yield for the IAEA was low and capri-cious.After some experimentation, we opted to remove themethyl group at C-3 on the premise that the requisite ter-tiary carbinol moiety in the natural product could be cre-ated in the last stages of the synthesis based on ProfessorLeo Paquette’s important finding in the Z series.34 Grati-fyingly, the internal alkylation of secondary derivative(E)-68 was superior to that of its tertiary syn-counterpart(E)-66 in terms of yield and reproducibility.The presence of the Kishi free radical inhibitor butylatedhydroxytoluene (BHT) was critical for the success of theintramolecular Diels–Alder reaction of (E)-oxonene 70,derived from key IAEA product (E)-69; the reaction de-livered a good yield of the desired adduct 71 (Scheme 27).The conversion of tricyclic intermediate 71 into our targetmolecule, (–)-cladiella-6,11-dien-3-ol (65), constitutedthe first total synthesis of an (E)-cladiellin (Scheme 27).One of the requirements of this total synthesis was totransform the ester functionality in intermediate 71 into anisopropyl group. This was achieved by reductive removalof the corresponding tertiary acetate with metallic potas-sium using the Barton protocol (72 → 73).35

Our synthesis of the (E)-cladiellin diterpene remained thefirst and only example until the very recent elegant workof Clark and co-workers.36 I confess that I had prayed ev-ery day for no one else to develop a synthesis of an (E)-cladiellin that would overshadow our work, but apparent-ly the prayer went unanswered.Furthermore, we demonstrated that our synthetic (E)-cla-diellin 65 could be transformed into other cladiellin mem-bers, such as (–)-cladiell-11-ene-3,6,7-triol (74), (–)-de-acetoxyalcyonin acetate (75), and (+)-polyanthellin A(76). Scheme 28 summarizes these highly stereo-, regio-,and chemoselective approaches, which take advantage ofthe reactivity and conformational rigidity of the (E)-oxo-nene moiety in the oxatricyclic skeleton of compound 65.

O

ODMBH

H

THPO

N OMe

OPMB

1. KHMDS 71%2. DDQ

Me

O

ODMBH

H

Cl

N

Me

OMe

OPMB

CCl4n-Oct3P

33%

O

ClH

HH

(+)-(3Z)-pinnatifidenyne (61)

BrAcO

O

BrH

HH

(+)-laurencin (45)

anti syn

O

OHH

H

THPO

N

Me

OMe

OPMB

LiHMDS THF86%

O

ClH

H

THPO

N

Me

OMe

OPMB

DDQ

O

ClH

H

Br

N

Me

OMe

OPMB

1. H+

2. [Br]

1. H+; 2. [Cl]IAEA/chlorination

chlorination/IAEA

CCl4n-Oct3P

87%

O HH

H

N

O

Me

Me

OH

OPMB

O HH

H

N

O

Me

Me

Cl

OPMB

α,α'-cis α,α'-cis

α,α'-cis

cis-anti (–)62

63

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46 D. Kim ACCOUNT


Scheme 28 Transformation of (E)-cladiellin 65 into other cladiellins

5 Synthesis of α,α′-trans-Disubstituted Medi-um-Ring Oxacyclic Marine Natural Products

I hope the above discussion has demonstrated that ourIAEA methodology has substantial potential for achiev-ing substrate-controlled syntheses of α,α′-cis-disubstitut-ed medium-ring oxacyclic natural products.For the remainder of this account, I would like to describeour efforts directed toward the synthesis of α,α′-trans-di-substituted medium-ring oxacyclic natural products. OurIAEA methodology has not so far been well-suited for thesynthesis of α,α′-trans-disubstituted compounds.37 TheEvans asymmetric alkylation/RCM strategy, however,has become established as a successful protocol for theconstruction of medium-ring oxacyclic skeletons, bothα,α′-cis- and α,α′-trans-disubstituted, as illustrated withoxocenes in Scheme 29.We had been successful at exploiting the versatility of theα-alkoxy-substituted N,N-dimethylamide functionalityand the substrate-controlled strategy, and thus we askedourselves whether we could synthesize α,α′-syn- or α,α′-anti-disubstituted RCM substrates specifically without re-course to a chiral auxiliary. The embedded oxygen atomshighlighted in bold red in Scheme 29 suggested a way toemploy what we call the ‘protecting group dependent’ al-

Scheme 26 Construction of both (Z)- and (E)-oxonenes by intramo-lecular amide enolate alkylation

O

H

HOBn

BnO

NMe

O

Me

O

HOBn

BnO

NMe

O

Me Cl

KHMDSTHF

80%unoptimized3

2

(Z)-66: (Z)-C-3 3°/syn (Z)-67: (Z)-C-3 3°/α,α'-cis-syn

KHMDSTHF

0 ~ 40%capricious

O

H

HOBn

NMe

O

Me

BnO

O

HOBn

NMe

O

Me

BnO

Cl

(E)-66: (E)-C-3 3°/syn (E)-67: (E)-C-3 3°/α,α'-cis-syn

E

Z

(–)-cladiella-6,11-dien-3-ol (65)

O

H

H

H

HOH

E

(–)-ophirin B (64)

O

H

H

H

HOAc

AcO

OAc

Z

LiHMDSTHF

92%O

H

HH OTr

NMe

O

Me

TBDPSO

O

HH OTr

NMe

O

Me

TBDPSO

Cl

(E)-68: (E)-C-3 2°/syn (E)-69: (E)-C-3 2°/α,α'-cis-syn

E

32

Scheme 27 Completion of the synthesis of (–)-cladiella-6,11-dien-3-ol (65)

O

MeO2C

H

H

H

HH OTr

O

H

HH OTr

MeO2C

BHTxylene, reflux

1 h

85%

O

H

H

H

HO

O

H

H

H

HOH

O

H

H

H

HH OTr

AcO

O

H

H

H

HH OH

K, t-BuNH218-crown-6

THF

r.t., 1 h55%

(3 steps from 71)

Paquettereaction

7071

72 73

(–)-cladiella-6,11-dien-3-ol (65)

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kylation/RCM strategy, which is essentially a substrate-controlled version of the Evans–Crimmins asymmetric al-kylation/RCM strategy.Itomanallene A, a C15 acetogenin with a 2,10-dioxabicyc-lo[7.3.0]dodecene skeleton, was isolated by the Suzukigroup from Laurencia intricata in 2002 (Figure 3).38 Thestructure and absolute configuration of its two previouslyisolated diastereomeric congeners (–)-isolaurallene (77)39and (+)-neolaurallene (78)40 had already been firmly es-tablished based on X-ray crystallographic studies.The relative stereochemistry of the bicyclic skeleton ofitomanallene A was established through extensive spec-troscopic studies. In particular, NOE interactions betweenH-6 and H-4 and between H-6 and H-7 were supportive ofthe assigned cis-relative stereochemistry of the tetrahy-drofuran ring in the compound. Judging from the strongpositive rotation of itomanallene A, its bromoallene moi-ety would be assigned as S by the application of Lowe’srule.41 Because the relative stereochemistry between thedioxabicyclic skeleton and the bromoallene unit in itoma-nallene A could not be determined by spectroscopic meth-ods, the two compounds 79a and 79b depicted in Figure 3were proposed as possible structures of itomanallene A.

The structural features of this dioxabicyclic marine natu-ral product that most appealed to us were the α,α′-trans-disubstituted oxonene and the α,α′-cis-disubstituted tetra-

Scheme 29 Evans–Crimmins asymmetric alkylation/ring-closing metathesis versus protecting group dependent substrate-controlled alkyla-tion/ring-closing metathesis

Xc

O

O

OBnH

H Xc

O

O

OBnH

H

Xc

O

O

OBnH

HH

Xc

O

O

OBnH

HH

Xc

O

O

OBnH

HH

Xc

O

O

OBnH

HH

Xc = chiral auxiliary

Evans–Crimmins Asymmetric Alkylation/RCM

RCM RCM

α,α'-syn α,α'-cis α,α'-trans α,α'-anti

N

O

O

OPG1H

HH

Me

Me

N

O

O

OPG2H

HH

Me

Me

α,α'-cis α,α'-trans

N

O

O

OPG1H

HH

Me

Me

N

O

O

OPG2H

HH

Me

Me

α,α'-syn α,α'-anti

RCM RCM

O

OPG2H

H

O

NMe

Me

O

OPG1H

H

O

NMe

Me

'Protecting Group Dependent' Substrate-Controlled Alkylation/RCM

α-alkoxy-substituted N,N-dimethylamide

?

Figure 3 Representative medium-ring ether marine natural productswith a 2,10-dioxabicyclo[7.3.0]dodecene skeleton

(S)

O

H

H

Br

H

H

OH

H

Br H(+)-neolaurallene (78)

(R)

O

H

H

Br

H

H

OH

H

H Br(–)-isolaurallene (77)

(S)

O

H

H

Br

H

H

OH

H

Br H

(S)

O

H

H

Br

H

H

OH

H

Br H79b79a

α,α'-cis

α,α'-trans

α,α'-trans

α,α'-cis

α,α'-trans

α,α'-trans

α,α'-trans

α,α'-cis

two proposed structures of (+)-itomanallene A

1

54

67

13

10 9

12

153

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48 D. Kim ACCOUNT


hydrofuran. I would like to describe our asymmetric totalsynthesis and consequent structure revision of itomanal-lene A which epitomizes our completely substrate-con-trolled approach to the synthesis of α,α′-trans-disubstituted medium-ring oxacyclic natural products.42

Our first objective was to confirm the relative stereochem-istry between the dioxabicyclic core and the bromoalleneappendage of itomanallene A. For simplicity, we initiallyopted to synthesize ent-79a and 79b instead of the origi-nally proposed structures 79a and 79b. This decisionturned out to be a fortuitous one. Our retrosynthetic planfor the substrate-controlled synthesis of ent-79a and 79b,as shown in Scheme 30, once again hinged upon the ver-satility of the α-alkoxy-substituted N,N-dimethylamidefunctionality.We envisioned that bicyclic α-alkoxy-substituted amide81 could be elaborated to both ent-79a and 79b by instal-lation of the respective bromoallene units through the in-termediacy of bicyclic bromo-substituted aldehyde 80.We were confident that the α,α′-cis-disubstituted tetrahy-drofuran ring in bicyclic amide 81 could be constructed ina stereoselective manner through the IAEA reaction of to-sylate 82, which in turn could be readily prepared fromoxonene intermediate 83. We initially reasoned that thenine-membered ether ring 83 could be constructed by theRCM reaction of bis-alkene 84.42

In this plan, the syn stereochemical relationship betweenC-12 and C-13 (corresponding to the final product) inRCM substrate 84 would be established by the manipula-tion of the α-alkoxy-substituted N,N-dimethylamide moi-ety in 85 using our direct ketone synthesis/L-Selectridereduction protocol. For the greater challenge representedby the pivotal α,α′-anti stereochemistry of ether 85, we en-visaged that this would be addressed through the ‘che-moselective chelation-controlled’ intermolecular amideenolate alkylation of 86. Further analysis suggested thatalkylation substrate 86 would be readily accessible fromknown 4-methoxybenzyl (PMB) protected (S)-glycidol 88via the installation of the C-6/C-7-syn stereochemistry bychelation-controlled nucleophilic addition to aldehyde 87.A significant feature of this approach is that it showcasesthe versatility of α-alkoxy-substituted amide enolate al-kylation in establishing both sets of relative α,α′-oxyme-thine configurations without recourse to additional chiralauxiliaries.Scheme 31 presents a summary of our synthesis and struc-tural revision of (+)-itomanallene A and our synthesis ofent-neolaurallene, with particular emphasis on the mostsalient stereo-, regio-, and chemoselective steps.To this end, the C-6/C-7-syn stereochemistry in key alkyl-ation substrate 86 was established in the presence of an α-alkoxy-substituted amide through the chemoselectivechelation-controlled nucleophilic addition of allyltributyl-stannane to aldehyde 87, derived from known PMB-pro-tected (S)-glycidol 88,43a using the method of Keck.44

The significant challenge of achieving the critical α,α′-anti stereochemistry in α-alkoxy-substituted amide 85was successfully addressed by the chemoselective chela-tion-controlled intermolecular amide enolate alkylation of86. In this scenario, the alkylating agent approaches theless-hindered convex face of cup-shaped chelated enolateintermediate E, in which the bulky group at C-6 prefers tobe located, to afford the desired product 85 as essentiallya single isomer.45 It is worth noting that the PMB-protect-ed hydroxy group participates in the chelation in prefer-ence to the triisopropylsilyl (TIPS) protected one, whichis known to be a poor coordinating group.As planned, the syn stereochemical relationship betweenC-12 and C-13 in RCM substrate 84 was established bythe manipulation of the α-alkoxy-substituted N,N-dimeth-ylamide in 85 through the intermediacy of ketone 89 usingour direct ketone synthesis/L-Selectride reduction proto-col.21,27

Scheme 30 Retrosynthetic plan for compounds ent-79a and 79b

intra-molecular

amide enolatealkylation

O

H

H

BnO

H

H

OH

O

H

H

BnO

H

H

O

TsO

OOPMB

OTIPS

H

H

BnO

H

HO

OPMB

OTIPS

H

H

BnO

H

H

81 82

RCM

83 84

inter-molecular

amide enolatealkylation

86

NMe

O

Me

4

NMe

O

Me

O

N

OPMB

OTIPS

H

HH85

α,α'-anti

O

MeMe

12

1213

ent-79a(R)

O

H

H

Br

H

H

OH

H

H Br

O

H

H

Br

H

H

OH

80 H

O

7

(S)

O

H

H

Br

H

H

OH

H

Br H

79b

α,α'-cis

OOPMB

OTIPS

H

H

O

N

Me

Me

6

bromoallenesynthesis [Br] and [H]

RM and [H]

OOPMB

O

H

O

N

Me

Me

6

88 (known)

OOPMBH

6

87

13

RM

76

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Scheme 31 Summary of the asymmetric total synthesis and structure revision of (+)-itomanallene A

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50 D. Kim ACCOUNT


To our great disappointment, upon conducting the hithertouninvestigated RCM of C-6/C-7-syn,α,α′-anti,C-12/C-13-syn bis-alkene 84, only a low yield of the desired oxonene83 (~20%) was obtained despite a considerable amount ofeffort. The rationale that a cyclic constraint might facili-tate the RCM prompted us to construct the five-memberedring first. To this end, the α,α′-cis-disubstituted tetrahy-drofuran ring was constructed in a stereoselective mannerthrough the IAEA reaction of tosylate 90 as anticipated,probably via H-eclipsed transition state F. Gratifyingly,the resulting tetrahydrofurano-fused diene 91 underwentRCM using Grubbs’ second generation catalyst to pro-duce key bicyclic oxonene 81 in 70% yield.When facing obstacles throughout my career, such as theabove-mentioned inefficient RCM, I have frequentlyovercome them using hunch-based reasoning rather thanwell thought out chemical rationale. On the plus side, thisalchemical journey has often led to serendipitous discov-eries. When I could not properly rationalize these, circum-stances led me to use vague expressions, such as ‘might’,‘probably’, ‘presumably’, and ‘we are still developing arationale for’ in my publications. As a result, very keen re-viewers occasionally gave me horrendous scores on‘scholarly presentation’. Recently, I have had the wonder-ful and extremely fortunate opportunity to collaboratewith a superb young computational chemist, Dr. Robert S.Paton (University of Oxford). Nowadays, I can walk thestreets of Seoul with my head held high, exuding a confi-dence which used to be foreign to my chemical life.It was known that the relative stereochemistry of the in-cipient cyclic ether oxygen atom with respect to each ofthe adjacent oxygen substituents, as well as the α,α’-rela-tive stereochemistry, could exert subtle conformationaleffects on the rate of the RCM to give oxonenes.42,46 Togain insight into these conformational effects, Dr. Patonembarked on computational studies of the RCM reactionsof the eight possible diastereomers of 84, and for (Z)-2,3,4,7,8,9-hexahydrooxonine he located the global mini-mum AS2 conformation G, as depicted in Scheme 31.47

While simplifying the process by turning protectinggroups into methyl groups in the model, the stabilities ofthe open chain (i.e., with terminal alkenes) and ring-closed forms (following RCM) of the eight possible dia-stereomers of 84 were calculated in an attempt to gaugethe effect of stereochemistry on the energetics of theRCM. The mechanism of ring closure involves rutheni-um–alkylidene and metallocycle intermediates and transi-tion states, but the quantum chemical calculationsrequired to study these species being such flexible sys-tems are computationally intractable.Thus, we focused instead on the relative stabilities of thediastereomeric reactants and cyclized products to givevalues for ΔΔErxn; this enabled us to rank the systems interms of thermodynamic favorability. The open-chain re-actant energies all lie within 0.5 kcal/mol of each other be-cause the reactants are flexible and may adopt a numberof conformations. Following RCM, however, the cyclized

product stability is more variable, and it is this energy thatdictates the ΔΔErxn value.With the exception of one diastereomer, all the systemsshowed a preference for the asymmetric AS2 conforma-tion. In AS2 conformation G, preferentially adopted bythe ring, one of the dihedral angles (ΘCCCH = 20.8°) is par-tially eclipsing (Scheme 31). In nearly all of the systems,a β-alkoxy group pointed away from the ring, presumablyto avoid destabilization from an eclipsing CCCO interac-tion. In α,α′-trans-disubstituted diastereomer I, whichcorresponds to the stereochemistry of 84, the eclipsingCCCO interaction is present and results in the destabiliza-tion of this structure and retardation of the ring closure.Diastereomer I had less favorable reaction energy in com-parison with the other diastereomers – how unlucky wewere that our RCM substrate happened to be the worstsystem! – and this analysis is consistent with the fact thatthe attempted RCM of 84 proceeded in



and 79b. Incidentally, the C-4 epimer of ent-79a corre-sponds to the enantiomeric form of neolaurallene (ent-78).To this end, the requisite α,α′-trans-disubstituted tetrahy-drofuran stereochemistry could be secured by the forma-tion of major isomer 91′ upon exposure of cyano tosylate90′ to lithium hexamethyldisilazide (LiHMDS) using theINAA methodology based on the pioneering work ofStork and co-workers50 and subsequent investigations byFleming and co-workers.51

Many of the extant applications of this INAA methodolo-gy have involved the stereoselective construction of aquaternary center by taking advantage of the relativelysmall size and powerful nucleophilicity of the nitrile func-tionality. However, the presence of an acidic proton in α-unsubstituted cases, such as the above, raises a concern re-garding the potential loss of the stereochemical integrityduring the cyclization.An equilibration experiment to probe the relative stabilityof the isomers showed that the α,α′-trans-isomer is morestable than the corresponding cis one by a 2:1 margin.Furthermore, from a deuterium incorporation study aswell as the separate resubjection of the isolated isomers tothe reaction conditions, we were able to establish that theselectivity ratio of INAA arises from a kinetically con-trolled process under the cyclization conditions. Internalalkylation of the linear, N-metalated nitrile anion generat-ed under the reaction conditions gave the desired α,α′-trans-disubstituted tetrahydrofuran as the major product.We reasoned that the intermediate passes through the ge-ometry of transition state H, which benefits from stereo-electronic stabilization by placing the carbon–nitrile bondantiperiplanar to an oxygen lone pair on the ether oxy-gen.47,52

Intermediate 91′ was then transformed into 79c and ent-78in an analogous manner to derivative 91, except that inthis case aldehyde intermediate 80′ was derived by reduc-tion of the nitrile function with DIBAL-H.The spectroscopic characteristics and optical rotation ofour synthetic material 79c, corresponding to a C-4 epimerof one of the proposed structures, compound 79b, were ingood agreement with those reported for natural (+)-itoma-nallene A. Based on this synthesis, the structure of (+)-ito-manallene A should be revised to that shown in Scheme31. In addition, the spectroscopic and optical rotation datafor our synthetic compound C-4-epi-ent-79a, correspond-ing to ent-78, were in close agreement with those of natu-ral neolaurallene with the exception of the sign for theoptical rotation.

6 General Synthetic Plan for Dioxabicyclic Bromoallene Marine Natural Products Having either a 2,10-Dioxabicyclo[7.3.0]do-decene or 2,9-Dioxabicyclo[6.3.0]undecene Skeleton

The above-described first asymmetric total synthesis andconsequent structure revision of (+)-itomanallene A pro-vides a versatile strategy for the synthesis of both α,α′-cis-and α,α′-trans-disubstituted tetrahydrofurans in such di-oxabicylic marine natural products and related structuresthrough the judicious choice of an amide enolate versus anitrile anion, respectively, for the intramolecular alkyla-tion. It is worth mentioning that it was our casual interestin the comparative stereoselectivity of branched ester eno-lates versus linear nitrile anions in intramolecular alkyl-ations that launched a campaign that first began with ourunintended synthesis of brefeldin A (see Section 2), andmore than a decade later blossomed into a general strategyfor the construction of both α,α′-cis- and α,α′-trans-disub-stituted tetrahydrofurans in dioxabicylic marine naturalproducts.Based on the insights acquired during our synthesis andstructure revision of itomanallene A (79c), and employingas a common starting material glycidol, which is commer-cially available in both enantiomeric forms, we designeda general synthetic strategy to encompass the creation ofany arbitrary relative α,α′-oxymethine configurations inany of 32 biogenetically plausible stereoisomeric dioxab-icyclic bromoallene marine natural products having eitherthe 2,10-dioxabicyclo[7.3.0]dodecene or 2,9-dioxabicyc-lo[6.3.0]undecene skeleton. Scheme 32 shows our generalsynthetic plan for the half of the 32 isomeric natural prod-ucts that are derived from (S)-glycidol. This might benearly illegible given the minute fonts used; the other halfderived from enantiomer (R)-glycidol are not shown be-cause of space limitations.I am really good at and fond of drawing these schemes –in particular complicated ones, such as Scheme 32. Onone occasion, I showed off the two schemes covering all32 isomers to my student, but she seemed unappreciative.It was then that I realized she thought I intended that shesynthesize all of them, and her scowl meant that sheviewed my masterpieces as a life sentence of hard labor!Since we had developed optional access to α,α′-cis- andα,α′-trans-disubstituted tetrahydrofurans based on usingIAEA and INAA protocols, respectively, all we neededfor the execution of the general scheme was to secure themedium-sized ring α,α′ stereochemistry complementaryto that obtained via the above-mentioned chemoselectivechelation-controlled alkylation (86 → 85, see Section 5).To this end, we pinned our initially confident hopes for asolution on our ‘dianion’ alkylation methodology, as de-picted in Scheme 33.

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52 D. Kim ACCOUNT


The dianion alkylation of hydroxy-containing α-alkoxy-substituted amides 92a–d having various substituents atC-6 (based on the final natural product) [R = Et,CH2CH2OBn, CH2CH2CH2OBn, andCH2CH(OCH2CH2O), respectively] offered serviceablesyn/anti stereoselectivity (ca. 6–9:1) (Scheme 33). Wehave utilized this reaction as a key step for the substrate-controlled total synthesis of medium-ring oxacyclic natu-ral products in our laboratories.28a,53 The observed stere-oselectivity could be rationalized by empirical model I,with the electrophile approaching the least-hindered sideof the H,H-eclipsed conformation.To our surprise and disappointment, our initial effort toestablish the desired complementary α,α′-cis-disubstitut-ed oxonene stereochemistry via dianion alkylation ofPMB-protected α-alkoxy-substituted amide 92e (R =CH2OPMB) gave very disappointing stereoselectivity(syn/anti = 1.1:1) and chemical yield (54%).47 It is worthmentioning that the triisopropylsilylation of 92e providedsubstrate 86, required for the chemoselective chelation-controlled intermolecular amide enolate alkylation in ourearlier described synthesis of (+)-itomanallene A (79c).42The use of 92e in this sequence would have simplified ourgeneral approach to our target compounds, but the virtualabsence of stereoselectivity in the key step reminded us ofthe old adage, “The best laid schemes of mice and men gooften awry, and leave us nothing but grief and pain forpromised joy!”

We reasoned that the use of the corresponding TIPS-pro-tected hydroxymethyl group might avoid any potential in-terference owing to chelation because TIPS ethers areknown to be poor coordinating groups, unlike their PMBderivatives. We were delighted to find that the applicationof our protocol to TIPS-protected α-alkoxy-substitutedamide 92f (R = CH2OTIPS)47 proved successful, and

Scheme 32 General synthetic plan for 16 biogenetically plausible dioxabicyclic bromoallene marine natural products having either a 2,10-dioxabicyclo[7.3.0]dodecene or 2,9-dioxabicyclo[6.3.0]undecene skeleton from (S)-glycidol

General Synthetic Strategy

H

OOH

O

OH

HH

Br

H

H Br

H

(R)

unknownα,α'-trans

(S)

O

H

H

BrH

H

OH

H

Br Hunknown

α,α'-cis(S)

O

H

H

BrH

H

OH

H

Br Hα,α'-trans

(+)-itomanallene A(revised)

ethyl halideallyl halide

α,α'-trans

α,α'-trans

O

OH

HH

Br

H

Br H

H

(S)

(+)-laurallene

α,α'-trans

α,α'-trans

α,α'-cis

RCM/IAEAINAA/RCM

OOPMB

OTIPSH

H

O

H

NMe

Me

OOTIPS

OHH

H

O

H

NMe

Me

OOPMB

OTIPSH

H

ON

MeMe

OOTIPS

OHH

H

ON

MeMe

'chemoselective chelationcontrolled' alkylation

withdifferent electrophile

'dianion' alkylation with

different electrophile

(S)-glycidol

allyl halide ethyl halide

(R)

O

H

H

BrH

H

OH

H

H Brent-(+)-neolaurallene

(unknown)

α,α'-trans

α,α'-trans

O

OH

HH

Br

H

H Br

H

(R)

(–)-nipponallene

α,α'-trans

α,α'-trans

O

OH

HH

Br

H

Br H

H

(S)

(+)-pannosalleneα,α'-trans

(R)

O

H

H

BrH

H

OH

H

H Br(–)-Isolaurallene

α,α'-cis

α,α'-trans

α,α'-cis

(R)

O

H

H

BrH

H

OH

H

H Brα,α'-trans

ent-(+)-itomanallene A(ent-proposed, unknown)

α,α'-cis

(S)

O

H

H

BrH

H

OH

H

Br H(+)-itomanallene A

(proposed, unknown)

α,α'-trans

α,α'-cis

IAEA/RCMINAA/RCM

(R)

O

H

H

BrH

H

OH

H

H Brunknown

α,α'-cis

α,α'-cis

(S)

O

H

H

BrH

H

OH

H

Br Hunknown

α,α'-cis

α,α'-cis

IAEA/RCMINAA/RCM

O

OH

HH

Br

H

H Br

H

(R)

unknownα,α'-cis

O

OH

HH

Br

H

Br H

H

(S)

unknown

α,α'-trans

α,α'-cis

α,α'-cis

RCM/IAEAINAA/RCM

O

OH

HH

Br

H

H Br

H

(R)

unknown

α,α'-trans

α,α'-cis

O

OH

HH

Br

H

Br H

H

(S)

unknownα,α'-cis

α,α'-cis

OOTIPS

OHH

H

O

H

NMe

Me

O

OH

O

N

Me

Me

OTIPS

H

HH

OOPMB

OTIPSH

H

O

H

NMe

Me

O

OTIPS

O

N

Me

Me

OPMB

H

HH

**

*

Mitsunobu reaction

Scheme 33 Stereoselectivity in dianion alkylation

OR

OH

H

H

O

E H

N

Me

Me

OR

OH

H

H

O

N

Me

Me

6

O

LiON

Me

Me

H H

R

OLi

6

E+

LiHMDSTHF

E+

R Substrate no.Ratio

(syn/anti)

Et

CH2CH2OBn

CH2CH2CH2OBn

CH2CH(OCH2CH2O)

CH2OPMB

CH2OTIPS

92e

92f

9.3:1

6:1

6:1

6.3:1

37:1

1.1:1

I

92a

92b

92c

92d

E+

allyl bromide

ethyl iodide

ethyl iodide

allyl bromide

allyl bromide

allyl iodide

92 93

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treatment with LiHMDS in the presence of ethyl iodidegave the desired α,α′-syn-disubstituted ether 93f with ex-cellent stereoselectivity (syn/anti = 37:1; 91% total yield).Although I dread to write it this way, for reasons I have al-luded to earlier, we are still developing a rationale to ex-plain this relatively high degree of stereoselectivity.Incorporating the established methodologies for creatingany arbitrary relative α,α′-oxymethine configurations, themore sensible and easily legible Scheme 34 illustrates ourentirely substrate-controlled sequences from (S)-glycidol(97) to some of those marine natural products among the32 having either the 2,10-dioxabicyclo[7.3.0]dodecene or2,9-dioxabicyclo[6.3.0]undecene skeleton which havebeen isolated from natural sources to date.47 The com-pounds with the former skeleton are (–)-isolaurallene(77),39 the enantiomeric form of natural (+)-neolaurallene(ent-78),40 and (+)-itomanallene A (79c),38 while thosewith the latter skeleton are (+)-laurallene (94),54 (–)-nip-ponallene (the bromoallene diastereomer of laurallene;not shown in Scheme 34),55 and (+)-pannosallene (95).56

Our general approach to establish the α,α′-relative stereo-chemistry of the medium-sized ring (oxonene or oxocene)and tetrahydrofuran involved the judicious pairing of ourprotecting group dependent intermolecular amide enolatealkylation (either chemoselective chelation-controlled ordianion alkylation) with either our intramolecular amideenolate or intramolecular nitrile anion alkylation. The ap-plication of this approach offered us optional access toany of these dioxabicyclic bromoallene marine natural

products. The requisite bromoallene appendage could beelaborated via application of the stereoselective Overmanprotocol to either the corresponding propargylic alcoholor its diastereomer, obtained using a Mitsunobu inversionreaction.More specifically, our chemoselective chelation-con-trolled intermolecular amide enolate alkylation (86 → 85)and INAA were utilized to establish the α,α′-trans-disub-stituted oxonene and tetrahydrofuran stereochemistry, re-spectively, in itomanallene A (79c) and ent-(+)-neolaurallene (ent-78). Conversely, the intermolecular di-anion alkylation strategy (92f → 93f) and INAA providedaccess to the α,α′-cis-disubstituted oxonene skeleton andα,α′-trans-disubstituted tetrahydrofuran, respectively, forthe synthesis of (–)-isolaurallene (77). In addition, the useof an allyl halide electrophile in place of an ethyl halidefor the intermolecular dianion alkylation (92f → 96) en-abled us to construct the α,α′-trans-disubstituted oxo

account 33 - thieme-connect.de · account 33 accountintramolecular enolate alkylation: from...

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