Issue 21, 2017

Palladium-catalyzed carbonylative Sonogashira coupling of aryl diazonium salts with formic acid as the CO source: the effect of 1,3-butadiene

Abstract

An efficient carbonylative cross-coupling of aryl diazonium salts with terminal alkynes using formic acid as the CO source has been developed. Various useful alkynones were produced in moderate to good yields. Notably, 1,3-butadiene was found to play a crucial role in this transformation.

Graphical abstract: Palladium-catalyzed carbonylative Sonogashira coupling of aryl diazonium salts with formic acid as the CO source: the effect of 1,3-butadiene

Supplementary files

Article information

Article type
Communication
Submitted
29 Aug 2017
Accepted
28 Sep 2017
First published
29 Sep 2017

Catal. Sci. Technol., 2017,7, 4924-4928

Palladium-catalyzed carbonylative Sonogashira coupling of aryl diazonium salts with formic acid as the CO source: the effect of 1,3-butadiene

F. Wu, J. Peng, X. Qi and X. Wu, Catal. Sci. Technol., 2017, 7, 4924 DOI: 10.1039/C7CY01773A

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