Stereospecific C–S Bond Formation from Chiral Tertiary Alcohols by Quinone-Mediated Oxidation–Reduction Condensation Using Alkyl Diphenylphosphinites and Its Application to the Synthesis of a Chiral Tertiary Thiol-Reference-Cited by-同舟云学术

Stereospecific C–S Bond Formation from Chiral Tertiary Alcohols by Quinone-Mediated Oxidation–Reduction Condensation Using Alkyl Diphenylphosphinites and Its Application to the Synthesis of a Chiral Tertiary Thiol

Published:2006-05 Issue:5 Volume:79 Page:780-790
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Ikegai Kazuhiro,Pluempanupat Wanchai,Mukaiyama Teruaki

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference55 articles.

1. Stereospecific synthesis of chiral tertiary alkyl-aryl ethers via Mitsunobu reaction with complete inversion of configuration

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3. Microbial approach to the practical monofluorinated chiral synthons

4. Enantioselective Synthesis of α-Methyl-d-cysteine and Lanthionine Building Blocks via α-Methyl-d-serine-β-lactone

5. Stereoselective substitution of (R)-2-(sulfonyloxy)nitriles with sulfur nucleophiles

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