Issue 36, 2011

A general and efficient approach to 2H-indazoles and 1H-pyrazoles through copper-catalyzed intramolecular N–N bond formation under mild conditions

Abstract

A new efficient copper-catalyzed intramolecular amination reaction has been developed to readily synthesise a wide variety of multi-substituted 2H-indazole and 1H-pyrazole derivatives from easily accessible starting materials under mild conditions. A highly selective ligand for estrogen receptor β was prepared in three steps by employing this method.

Graphical abstract: A general and efficient approach to 2H-indazoles and 1H-pyrazoles through copper-catalyzed intramolecular N–N bond formation under mild conditions

Supplementary files

Article information

Article type
Communication
Submitted
30 Jun 2011
Accepted
22 Jul 2011
First published
09 Aug 2011

Chem. Commun., 2011,47, 10133-10135

A general and efficient approach to 2H-indazoles and 1H-pyrazoles through copper-catalyzed intramolecular N–N bond formation under mild conditions

J. Hu, Y. Cheng, Y. Yang and Y. Rao, Chem. Commun., 2011, 47, 10133 DOI: 10.1039/C1CC13908H

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