Issue 29, 2014

Synthesis of 2,3-dihydro-1H-indazoles by Rh(iii)-catalyzed C–H cleavage of arylhydrazines

Abstract

A rhodium-catalyzed efficient method for the synthesis of 2,3-dihydro-1H-indazoles is described. The reaction of arylhydrazines with olefins results in the corresponding 2,3-dihydro 1H-indazoles with exclusive regioselectivity via C–H bond activation. The utility of the methodology is illustrated by a rapid synthesis of 1H-indazoles under mild reaction conditions in half an hour.

Graphical abstract: Synthesis of 2,3-dihydro-1H-indazoles by Rh(iii)-catalyzed C–H cleavage of arylhydrazines

Supplementary files

Article information

Article type
Paper
Submitted
05 May 2014
Accepted
10 Jun 2014
First published
11 Jun 2014

Org. Biomol. Chem., 2014,12, 5469-5476

Synthesis of 2,3-dihydro-1H-indazoles by Rh(III)-catalyzed C–H cleavage of arylhydrazines

J. Yao, R. Feng, C. Lin, Z. Liu and Y. Zhang, Org. Biomol. Chem., 2014, 12, 5469 DOI: 10.1039/C4OB00921E

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