Preparation of Enantiomerically Pure ?-Silylcarboxyl Derivatives by Asymmetric 1,4-Addition toN-Enoyl-sultams. Preliminary Communication-Reference-Cited by-同舟云学术

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Preparation of Enantiomerically Pure ?-Silylcarboxyl Derivatives by Asymmetric 1,4-Addition toN-Enoyl-sultams. Preliminary Communication

Published:1986-10-29 Issue:7 Volume:69 Page:1542-1545
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Oppolzer Wolfgang,Mills Robert J.,Pachinger Werner,Stevenson Thomas

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference22 articles.

1. J. Chem. Soc., Chem. Commun. 1984, 28;

2. A synthesis of the prelog-djerassi lactone using open-chain stereocontrol based on allylsilane chemistry

3. Oxidative cleavage of silicon-carbon bonds in organosilicon fluorides to alcohols

4. (b) J. Chem. Soc., Chem. Commun. 1984, 29.

5. Camphor-DerivedN-Acryloyl andN-Crotonoyl Sultams: Practical Activated Dienophiles in AsymmetricDiels-alder Reactions. Preliminary Communication

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