Issue 1, 2015

O-Arylation with nitroarenes: metal-catalyzed and metal-free methodologies

Abstract

In this article, we focus on the introduction of nitroarene as an alternative electrophile for Caryl–O cross-coupling chemistry. In polar aprotic solvents and in the presence of a base at elevated temperature nitroarene undergoes cross-coupling with arylboronic acids or phenols under metal or metal-free reaction conditions. Compared to the conventional aryl halides, nitroarene provides highly attractive and environmentally friendly options for the synthesis of diaryl ether derivatives.

Graphical abstract: O-Arylation with nitroarenes: metal-catalyzed and metal-free methodologies

Article information

Article type
Focus
Submitted
04 Aug 2014
Accepted
22 Sep 2014
First published
23 Sep 2014

New J. Chem., 2015,39, 31-37

Author version available

O-Arylation with nitroarenes: metal-catalyzed and metal-free methodologies

M. Mondal, S. K. Bharadwaj and U. Bora, New J. Chem., 2015, 39, 31 DOI: 10.1039/C4NJ01293C

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