Issue 2, 2016

Nickel–glycerol: an efficient, recyclable catalysis system for Suzuki cross coupling reactions using aryl diazonium salts

Abstract

Nickel catalysed Suzuki reactions of phenyl boronic acids with aryl diazonium salts in glycerol as a reaction medium are reported. Various aryl diazonium salts were efficiently reacted with aryl boronic acids under optimized conditions to give the respective diaryl compounds in good to excellent yields. The base free conditions and use of glycerol as a solvent, which can be recycled successfully for up to five consecutive cycles, make the present protocol environmentally benign in nature.

Graphical abstract: Nickel–glycerol: an efficient, recyclable catalysis system for Suzuki cross coupling reactions using aryl diazonium salts

Supplementary files

Article information

Article type
Paper
Submitted
14 Jul 2015
Accepted
24 Nov 2015
First published
30 Nov 2015

New J. Chem., 2016,40, 1564-1570

Author version available

Nickel–glycerol: an efficient, recyclable catalysis system for Suzuki cross coupling reactions using aryl diazonium salts

J. M. Bhojane, S. A. Sarode and J. M. Nagarkar, New J. Chem., 2016, 40, 1564 DOI: 10.1039/C5NJ01833A

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