Electrophilic Sulphenylation of Silyl Ketene Acetals Derived from 3-Hydroxyesters. Diastereoselective Synthesis of Protected Epoxyalcohols-Reference-Cited by-同舟云学术

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Electrophilic Sulphenylation of Silyl Ketene Acetals Derived from 3-Hydroxyesters. Diastereoselective Synthesis of Protected Epoxyalcohols

Published:1988-10-05 Issue:10 Volume:17 Page:1683-1686
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Guanti Giuseppe,Banfi Luca,Narisano Enrica,Thea Sergio

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference15 articles.

1. Asymmetric hydrogenation of .beta.-keto carboxylic esters. A practical, purely chemical access to .beta.-hydroxy esters in high enantiomeric purity

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

3. Brominations of Cyclic Acetals from ?-Amino Acids and ?- or ?-Hydroxy Acids withN-Bromosucinimide

4. A stereocontrolled synthesis of the key intermediate of (+)-thienamycin from ()-(−)-3-hydroxybutyric acid esters

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1. Benzenesulfenyl Chloride;Encyclopedia of Reagents for Organic Synthesis;2013-04-22

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5. Benzenesulfenyl Chloride;Encyclopedia of Reagents for Organic Synthesis;2005-10-15

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