Issue 14, 2015

Decarboxylative acylation of arenes with mandelic acid derivatives via palladium-catalyzed oxidative sp2 C–H activation

Abstract

An efficient palladium catalyzed decarboxylative acylation of arenes with mandelic acid derivatives via oxidative sp2 C–H activation in the presence of tert-butyl hydroperoxide has been developed. The acylation reaction is assisted by a pyridine directing group. The starting materials are inexpensive and readily available. This method provides an economical and convenient way to synthesize aryl ketones.

Graphical abstract: Decarboxylative acylation of arenes with mandelic acid derivatives via palladium-catalyzed oxidative sp2 C–H activation

Article information

Article type
Paper
Submitted
08 Nov 2014
Accepted
05 Jan 2015
First published
06 Jan 2015

RSC Adv., 2015,5, 10641-10646

Decarboxylative acylation of arenes with mandelic acid derivatives via palladium-catalyzed oxidative sp2 C–H activation

X. Liu, Z. Yi, J. Wang and G. Liu, RSC Adv., 2015, 5, 10641 DOI: 10.1039/C4RA14107E

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