Issue 11, 2001

Synthesis of substituted hexa-3,5-dienoic acid methyl esters from conjugated dienones

Abstract

Substituted hexa-3,5-dienoic acid methyl esters (2) were conveniently prepared in one step by 1,2-carbonyl transposition of the corresponding dienones (1) using lead(IV) acetate and boron trifluoride–diethyl ether in benzene at room temperature.

Graphical abstract: Synthesis of substituted hexa-3,5-dienoic acid methyl esters from conjugated dienones

Article information

Article type
Paper
Submitted
07 Feb 2001
Accepted
04 Apr 2001
First published
04 May 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 1300-1303

Synthesis of substituted hexa-3,5-dienoic acid methyl esters from conjugated dienones

R. L. Nongkhlaw, R. Nongrum and B. Myrboh, J. Chem. Soc., Perkin Trans. 1, 2001, 1300 DOI: 10.1039/B101242H

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