Download PDF
Synthesis 2013; 45(11): 1469-1474
DOI: 10.1055/s-0033-1338412
paper
© Georg Thieme Verlag Stuttgart · New York

An Easy Direct Arylation of 3-Arylsydnones

Yiwen Yang
a   Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092, P. R. of China   Fax: +86(21)65983191   Email: kuangcx@tongji.edu.cn
b   College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing 314001, P. R. of China
,
Hao Gong
a   Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092, P. R. of China   Fax: +86(21)65983191   Email: kuangcx@tongji.edu.cn
,
Chunxiang Kuang*
a   Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092, P. R. of China   Fax: +86(21)65983191   Email: kuangcx@tongji.edu.cn
c   Key Laboratory of Yangtze River Water Environment, Ministry of Education, Siping Road 1239, Shanghai 200092, P. R. of China
› Author Affiliations
Further Information

Publication History

Received: 03 February 2013

Accepted after revision: 22 March 2013

Publication Date:
15 April 2013 (online)

    Permissions and Reprints All articles of this category


Abstract

An easy one-step synthesis of 3,4-diarylsydnones from 3-arylsydnones and arylboronic acids by Pd-catalyzed C–H bond activation is described.

Key words

arylation - sydnones - arylboronic acids - Pd(OAc)2 - C–H bond activation

Supporting Information

    for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
  • Supporting Information