Literature DB >> 24909452

Gold-catalyzed direct hydrogenative coupling of nitroarenes to synthesize aromatic azo compounds.

Xiang Liu1, Hai-Qian Li, Sen Ye, Yong-Mei Liu, He-Yong He, Yong Cao.   

Abstract

The azo linkage is a prominent chemical motif which has found numerous applications in materials science, pharmaceuticals, and agrochemicals. Described herein is a sustainable heterogeneous-gold-catalyzed synthesis of azo arenes. Available nitroarenes are deoxygenated and linked selectively by the formation of N=N bonds using molecular H2 without any external additives. As a result of a unique and remarkable synergy between the metal and support, a facile surface-mediated condensation of nitroso and hydroxylamine intermediates is enabled, and the desired transformation proceeds in a highly selective manner under mild reaction conditions. The protocol tolerates a large variety of functional groups and offers a general and versatile method for the environmentally friendly synthesis of symmetric or asymmetric aromatic azo compounds.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  arenes; azo compounds; gold; reduction; supported catalysts

Year:  2014        PMID: 24909452     DOI: 10.1002/anie.201404543

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


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