A General Method for the Synthesis of Both Enantiomers of Optically Pure β-Hydroxy Esters from (S)-(p-Chlorophenylsulfinyl)acetone Easily Obtainable by Kinetic Resolution with Bakers’ Yeast-Reference-Cited by-同舟云学术

A General Method for the Synthesis of Both Enantiomers of Optically Pure β-Hydroxy Esters from (S)-(p-Chlorophenylsulfinyl)acetone Easily Obtainable by Kinetic Resolution with Bakers’ Yeast

Published:1988-04 Issue:4 Volume:61 Page:1273-1279
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Fujisawa Tamotsu,Fujimura Atsushi,Sato Toshio

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/61/4/61_4_1273/_pdf

Reference31 articles.

1. Stereoselective Aldol Reactions withα-Unsubstituted Chiral Enolates

2. Acyclic stereoselection. 4. Assignment of stereostructure to .beta.-hydroxycarbonyl compounds by carbon-13 nuclear magnetic resonance

3. Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensation

4. Acyclic stereoselection. 8. A new class of reagents for the highly stereoselective preparation of threo-2-alkyl-3-hydroxycarboxylic acids by the aldol condensation

5. Enantioselective aldol condensations. 3. Erythro-selective condensations via zirconium enolates

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