Issue 9, 2016

Palladium-catalyzed alkoxycarbonylation of aryl halides with phenols employing formic acid as the CO source

Abstract

An efficient palladium-catalyzed alkoxycarbonylation of aryl halides with phenols has been developed. Various aryl benzoates have been isolated in good to excellent yields with formic acid as the CO source. The reaction proceeds smoothly under mild conditions and good functional group tolerance was observed.

Graphical abstract: Palladium-catalyzed alkoxycarbonylation of aryl halides with phenols employing formic acid as the CO source

Supplementary files

Article information

Article type
Paper
Submitted
16 Nov 2015
Accepted
03 Dec 2015
First published
07 Dec 2015

Catal. Sci. Technol., 2016,6, 3099-3107

Author version available

Palladium-catalyzed alkoxycarbonylation of aryl halides with phenols employing formic acid as the CO source

X. Qi, C. Li, L. Jiang, W. Zhang and X. Wu, Catal. Sci. Technol., 2016, 6, 3099 DOI: 10.1039/C5CY01957E

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