A Systematic Study on the Bakers’ Yeast Reduction of 2-Oxoalkyl Benzoates and 1-Chloro-2-alkanones-Reference-Cited by-同舟云学术

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A Systematic Study on the Bakers’ Yeast Reduction of 2-Oxoalkyl Benzoates and 1-Chloro-2-alkanones

Published:1992-03 Issue:3 Volume:65 Page:631-638
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Sakai Takashi,Wada Kou,Murakami Takahiko,Kohra Kiichiro,Imajo Norihisa,Ooga Yukihiro,Tsuboi Sadao,Takeda Akira,Utaka Masanori

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/65/3/65_3_631/_pdf

Reference55 articles.

1. Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine

2. Stereochemical control in yeast reduction

3. Enantiospecific synthesis of optically pure (3s)-hydroxy esters by the stereocontrolled yeast reduction of α-sulfenyl-β-ketoesters

4. On the steric course of baker's yeast mediated reduction of alkyl 4-azido- and 4-bromo-3-oxobutyrate. Synthesis of ()- and ()-carnitin

5. Stereochemical control of yeast reductions: Synthesis of R-(+)-α-lipoic acid

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4. Practical Two-Step Synthesis of an Enantiopure Aliphatic Terminal (S)-Epoxide Based on Reduction of Haloalkanones with “Designer Cells”;Advanced Synthesis & Catalysis;2007-12-10

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