Synthesis 2015; 47(01): 42-48
DOI: 10.1055/s-0034-1379073
paper
© Georg Thieme Verlag Stuttgart · New York

An Iron and Copper System Catalyzed C–H Arylation of Azoles with Arylboronic­ Acids

Wei-Ye Hu
Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)65680352   Email: zhangsl@suda.edu.cn
,
Pei-Pei Wang
Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)65680352   Email: zhangsl@suda.edu.cn
,
Song-Lin Zhang*
Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)65680352   Email: zhangsl@suda.edu.cn
› Author Affiliations
Further Information

Publication History

Received: 09 May 2014

Accepted after revision: 11 August 2014

Publication Date:
29 September 2014 (online)


Abstract

An efficient, environmentally friendly, and economical new method for arylation reactions of azoles with arylboronic acids via copper–iron-catalyzed C–H and C–B bond activation has been developed. The protocol tolerates a series of functional groups, such as methoxy, nitro, cyano, chloro, and trifluoromethyl groups.

Supporting Information

 
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