Stereochemical Control in Microbial Reduction. XXV. Additives Controlling Diastereoselectivity in a Microbial Reduction of Ethyl 2-Methyl-3-oxobutanoate-Reference-Cited by-同舟云学术

Stereochemical Control in Microbial Reduction. XXV. Additives Controlling Diastereoselectivity in a Microbial Reduction of Ethyl 2-Methyl-3-oxobutanoate

Published:1995-01 Issue:1 Volume:68 Page:285-288
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kawai Yasushi,Takanobe Kousuke,Ohno Atsuyoshi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/68/1/68_1_285/_pdf

Reference21 articles.

1. Stereoselektive Synthese von Alkoholen, IX. Absolute Konfiguration von Stegobinon

2. The use of microorganisms in organic synthesis. I. Microbiological asymmetric reduction of 2-methyl-3-oxobutyrates.

3. The stereoselective α-alkylation of chiral β-hydroxy esters and some applications thereof

4. Stereocontrol by introduction of a sulfur functional group in the asymmetric reduction of β-ketoesters with baker's yeast; preparation of optically pure 3s-hydroxydithioesters as a new chiral synthon of natural product synthesis

5. Diastereo- and enantioselective microbiological reduction of 2-methyl 3-oxoalkanoates

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