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Decarboxylative allylations of ester enolate equivalents†
Yamuna Ariyarathna,Jon A. Tunge
Organic & Biomolecular Chemistry Pub Date : 09/15/2014 00:00:00 , DOI:10.1039/C4OB01752H
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
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