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Copper-catalyzed carbonylative Suzuki coupling of aryl iodides with arylboronic acids under ambient pressure of carbon monoxide†
Laijin Cheng,Yanzhen Zhong,Zhuchao Ni,Hongyan Du,Fengli Jin,Qi Rong,Wei Han
RSC Advances Pub Date : 09/10/2014 00:00:00 , DOI:10.1039/C4RA08594A
Abstract

An efficient and ligandless nanocopper-catalyzed carbonylative cross-coupling of aryl iodides with arylboronic acids at ambient CO pressure in poly(ethylene glycol), has been developed. This protocol is general, practical, and recyclable, and offers an attractive alternative to the corresponding palladium-mediated carbonylative Suzuki process for the construction of biaryl ketone scaffolds.

Graphical abstract: Copper-catalyzed carbonylative Suzuki coupling of aryl iodides with arylboronic acids under ambient pressure of carbon monoxide
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