Volume 22, Issue 15
Preparative Organic Chemistry
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ChemInform Abstract: Stereoselective Reduction of Acyclic α-Bromo Esters.

Y. GUINDON

Y. GUINDON

Bio-Mega, Inc., Laval, Quebec, Can. H7S 2G5

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C. YOAKIM

C. YOAKIM

Bio-Mega, Inc., Laval, Quebec, Can. H7S 2G5

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R. LEMIEUX

R. LEMIEUX

Bio-Mega, Inc., Laval, Quebec, Can. H7S 2G5

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L. BOISVERT

L. BOISVERT

Bio-Mega, Inc., Laval, Quebec, Can. H7S 2G5

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D. DELORME

D. DELORME

Bio-Mega, Inc., Laval, Quebec, Can. H7S 2G5

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J.-F. LAVALLEE

J.-F. LAVALLEE

Bio-Mega, Inc., Laval, Quebec, Can. H7S 2G5

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First published: April 16, 1991

Abstract

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ChemInform Abstract

The α-bromo esters (I) are stereoselectively debrominated with tributylstannane to form predominantly the trans-substituted carboxylates (II). The mechanism and transition state are discussed.

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