cheminform abstract: chiral amine-triggered triple cascade reactions: a new approach to...

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ChemInform 2011, 42, issue 01 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Quinoline derivatives R 0410 DOI: 10.1002/chin.201124146 Chiral Amine-Triggered Triple Cascade Reactions: A New Approach to Function- alized Decahydroquinolines. — The highly enantio- and diastereoselective one-pot synthesis of the pharmaceutically interesting substructures (IV) involves a [2 + 2 + 2] annulation of cyclohexanone with nitroalkenes followed by aza-Henry hemiaminaliza- tion. — (RAI, A.; SINGH, A. K.; SINGH, S.; YADAV*, L. D. S.; Synlett 2011, 3, 335-340, http://dx.doi.org/10.1055/s-0030-1259320 ; Lab. Green Synth., Dep. Chem., Univ. Allahabad, Allahabad 211 002, India; Eng.) — Mais 24- 146

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Quinoline derivativesR 0410 DOI: 10.1002/chin.201124146

Chiral Amine-Triggered Triple Cascade Reactions: A New Approach to Function-alized Decahydroquinolines. — The highly enantio- and diastereoselective one-pot synthesis of the pharmaceutically interesting substructures (IV) involves a [2 + 2 + 2] annulation of cyclohexanone with nitroalkenes followed by aza-Henry hemiaminaliza-tion. — (RAI, A.; SINGH, A. K.; SINGH, S.; YADAV*, L. D. S.; Synlett 2011, 3, 335-340, http://dx.doi.org/10.1055/s-0030-1259320 ; Lab. Green Synth., Dep. Chem., Univ. Allahabad, Allahabad 211 002, India; Eng.) — Mais

24- 146

ChemInform 2011, 42, issue 01 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim