Issue 108, 2014

In situ generated nickel nanoparticle-catalyzed carbonylative Suzuki reactions of aryl iodides with arylboronic acids at ambient CO pressure in poly(ethylene glycol)

Abstract

A general in situ generated nickel nanoparticle-catalyzed carbonylative Suzuki reactions of aryl iodides with arylboronic acids at atmospheric CO pressure in poly(ethylene glycol) has been demonstrated. A wide range of aryl iodides and arylboronic acids can be coupled to the corresponding biarylketones with high yields even in the absence of an added ligand and at low catalyst loading. The nature of the active catalytic species is discussed.

Graphical abstract: In situ generated nickel nanoparticle-catalyzed carbonylative Suzuki reactions of aryl iodides with arylboronic acids at ambient CO pressure in poly(ethylene glycol)

Supplementary files

Article information

Article type
Communication
Submitted
22 Oct 2014
Accepted
13 Nov 2014
First published
13 Nov 2014

RSC Adv., 2014,4, 63216-63220

In situ generated nickel nanoparticle-catalyzed carbonylative Suzuki reactions of aryl iodides with arylboronic acids at ambient CO pressure in poly(ethylene glycol)

Y. Zhong, X. Gong, X. Zhu, Z. Ni, H. Wang, J. Fu and W. Han, RSC Adv., 2014, 4, 63216 DOI: 10.1039/C4RA10739J

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