Issue 63, 2019

Sterically hindered N-heterocyclic carbene/palladium(ii) catalyzed Suzuki–Miyaura coupling of nitrobenzenes

Abstract

Palladium-catalyzed denitrative Suzuki coupling of nitroarenes using 2-aryl-5-(2,4,6-triisopropylphenyl)-2,3-imidazolylidene[1,5-a]pyridines as the ligands is described. The key to success is the use of the NHC ligands which show strong donating ability and suitable steric hindrance allowing the successful oxidative addition of Ar–NO2 bonds. Both aromatic and aliphatic boronic acids are tolerated, and a variety of biphenyls and alkylarenes were obtained in good to excellent yields.

Graphical abstract: Sterically hindered N-heterocyclic carbene/palladium(ii) catalyzed Suzuki–Miyaura coupling of nitrobenzenes

Supplementary files

Article information

Article type
Communication
Submitted
17 Jun 2019
Accepted
09 Jul 2019
First published
15 Jul 2019

Chem. Commun., 2019,55, 9287-9290

Sterically hindered N-heterocyclic carbene/palladium(II) catalyzed Suzuki–Miyaura coupling of nitrobenzenes

K. Chen, W. Chen, X. Yi, W. Chen, M. Liu and H. Wu, Chem. Commun., 2019, 55, 9287 DOI: 10.1039/C9CC04634H

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