Stereoselective alkylation of dianions derived from chiral half-esters of monosubstituted malonic acids: asymmetric synthesis of α-alkyl α-amino acids and key synthetic intermediates for Hunteria and Aspidosperma indole alkaloids-Reference-Cited by-同舟云学术

Stereoselective alkylation of dianions derived from chiral half-esters of monosubstituted malonic acids: asymmetric synthesis of α-alkyl α-amino acids and key synthetic intermediates for Hunteria and Aspidosperma indole alkaloids

Published:1991 Issue:3 Volume: Page:525-535
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Ihara Masataka,Takahashi Masanobu,Taniguchi Nobuaki,Yasui Ken,Niitsuma Hiroko,Fukumoto Keiichiro

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1991/P1/P19910000525

Reference46 articles.

1. Enantioselective synthesis of useful chiral precursors, unsymmetrical propane-1,3-diol derivatives, from malonic acid

2. Asymmetric syntheses of chiral propane-1,3-diols starting from malonic acid

3. Highly enantiocontrolled total synthesis of (-)-protoemetinol

4. Asymmetric total synthesis of(–)-protoemetinol,(–)-protoemetine,(–)-emetine, and (–)-tubulosine by highly stereocontrolled radical cyclisations

5. J. W. Scott , in Asymmetric Synthesis, eds. J. D. Morrison and J. W. Scott, Academic, New York, 1984, vol. 4, p. 1;

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