Issue 4, 2012

Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids

Abstract

The first example of copper-catalyzed coupling of nitroarenes with arylboronic acids was developed, providing diaryl ethers in moderate to excellent yields. The efficiency of this reaction was demonstrated by compatibility with a wide range of groups. Moreover, the rigorous exclusion of air/moisture is not required in these transformations. Thus, the method represents a simple and facile procedure to access diaryl ethers. Preliminary mechanistic experiments using deuterium labeling showed that the oxygen atom was derived from water.

Graphical abstract: Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids

Supplementary files

Article information

Article type
Communication
Submitted
01 Dec 2011
Accepted
06 Feb 2012
First published
27 Feb 2012

Green Chem., 2012,14, 912-916

Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids

J. Zhang, J. Chen, M. Liu, X. Zheng, J. Ding and H. Wu, Green Chem., 2012, 14, 912 DOI: 10.1039/C2GC16539B

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