Issue 42, 2014

Decarboxylative allylations of ester enolate equivalents

Abstract

A variety of ester enolate equivalents are generated in situ and undergo α-allylation in high yields via palladium-catalyzed decarboxylative allylation. The transformations are complete within very short reaction times under ambient conditions. Synthesis of α-allylated acyl derivatives provides access to other carboxylic acid and alcohol derivatives via acyl group substitution or reduction.

Graphical abstract: Decarboxylative allylations of ester enolate equivalents

Supplementary files

Article information

Article type
Communication
Submitted
15 Aug 2014
Accepted
12 Sep 2014
First published
15 Sep 2014

Org. Biomol. Chem., 2014,12, 8386-8389

Decarboxylative allylations of ester enolate equivalents

Y. Ariyarathna and J. A. Tunge, Org. Biomol. Chem., 2014, 12, 8386 DOI: 10.1039/C4OB01752H

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