Asymmetric pinacol-type rearrangement of α-hydroxy methanesulfonates promoted by triethylaluminum — preparation of optically pure α-aryl and α-vinyl ketones

Asymmetric pinacol-type rearrangement of α-hydroxy methanesulfonates promoted by triethylaluminum — preparation of optically pure α-aryl and α-vinyl ketones —

Published:1983-01 Issue:45 Volume:24 Page:4997-5000
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Suzuki Keisuke,Katayama Eiji,Tsuchihashi Gen-ichi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. Molecular Rearrangements. XI. The Deamination of 1,1-Diphenyl-2-amino-1-propanol1

2. Synthesis of optically active 2-arylalkanoic acids by the use of 1,2-rearrangement of the aryl group

3. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines

4. Studies in Stereochemistry. XIII. The 1,2-Diphenyl-1-propanol System

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