Issue 61, 2016

AgNO3 as nitrogen source for rhodium(iii)-catalyzed synthesis of 2-aryl-2H-benzotriazoles from azobenzenes

Abstract

A new approach has been established for Rh(III)-catalyzed direct aza oxidative cyclization of non-prefunctionalized azobenzenes to provide 2-aryl-2H-benzotriazoles in good yields, in which AgNO3 instead of conventional azide reagents for the first time functions as the nitrogen source for the nitrogenation reaction. Preliminary mechanistic studies suggest that the Rh(III)-catalyst could account for the nitration reaction, and subsequently cationic silver species might both play a vital role in the fission of the nitrogen–oxygen bonds in nitro groups and promote aza oxidative cyclization.

Graphical abstract: AgNO3 as nitrogen source for rhodium(iii)-catalyzed synthesis of 2-aryl-2H-benzotriazoles from azobenzenes

Supplementary files

Article information

Article type
Communication
Submitted
24 May 2016
Accepted
28 Jun 2016
First published
28 Jun 2016

Chem. Commun., 2016,52, 9589-9592

Author version available

AgNO3 as nitrogen source for rhodium(III)-catalyzed synthesis of 2-aryl-2H-benzotriazoles from azobenzenes

J. Li, H. Zhou, J. Zhang, H. Yang and G. Jiang, Chem. Commun., 2016, 52, 9589 DOI: 10.1039/C6CC04341K

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