Copper-mediated annulation of 2-(1-arylvinyl) anilines and aryl nitrosos towards 2,3-diaryl-2H-indazoles

Literature Information

Publication Date 2016-10-20
DOI 10.1039/C6QO00540C
Impact Factor 5.281
Authors

Weiming Hu, Jin-Tao Yu, Suqin Liu, Yan Jiang, Jiang Cheng


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Abstract

A copper-mediated annulation of 2-(1-substituted vinyl) anilines and aryl nitrosos is developed for the synthesis of 2,3-diaryl pyrazoles. Compared with previously reported sequential azobenzene C–H ortho-acylation, reduction and cyclization procedures towards such frameworks, no external reductant was required during this cyclization, where the vinyl served as a formal innate reductant. Moreover, in this procedure, no selectivity was involved in the case of Ar1 ≠ Ar2.

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