Asymmetric synthesis of β-amino-γ-substituted-γ-butyrolactones: double diastereoselective conjugate addition of homochiral lithium amides to homochiral α,β-unsaturated esters-Reference-Cited by-同舟云学术

Asymmetric synthesis of β-amino-γ-substituted-γ-butyrolactones: double diastereoselective conjugate addition of homochiral lithium amides to homochiral α,β-unsaturated esters

Published:2007 Issue:24 Volume:5 Page:3922
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Cailleau Thaïs,Cooke Jason W. B.,Davies Stephen G.,Ling Kenneth B.,Naylor Alan,Nicholson Rebecca L.,Price Paul D.,Roberts Paul M.,Russell Angela J.,Smith Andrew D.,Thomson James E.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2007/OB/B712937H

Reference63 articles.

1. The conjugate addition of enantiomerically pure lithium amides as homochiral ammonia equivalents: scope, limitations and synthetic applications

2. General Route to 2,4,5-Trisubstituted Piperidines from Enantiopure β-Amino Esters. Total Synthesis of Pseudodistomin B Triacetate and Pseudodistomin F

3. Total synthesis of pamamycin 607: applications of remote asymmetric induction in organic synthesis

4. A Novel Synthesis of the Macrocyclic Spermidine Alkaloid (+)-(S)-Dihydroperiphylline

5. Asymmetric synthesis of (−)-deoxoprosophylline

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