Issue 16, 2000

Triisobutylaluminium promoted reductive rearrangement of substituted vinyl ethers to homologous alcohols

Abstract

Substituted vinyl ethers carrying electron-donating groups in the ether moiety undergo smooth oxygen to carbon rearrangement with triisobutylaluminium to afford chain extended alcohols.

Article information

Article type
Communication
Submitted
25 Apr 2000
Accepted
26 Jun 2000
First published
19 Jul 2000

Chem. Commun., 2000, 1507-1508

Triisobutylaluminium promoted reductive rearrangement of substituted vinyl ethers to homologous alcohols

B. du Roizel, M. Sollogoub, A. J. Pearce and P. Sinaÿ, Chem. Commun., 2000, 1507 DOI: 10.1039/B003277H

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