Synlett 2014; 25(10): 1425-1430
DOI: 10.1055/s-0033-1341244
letter
© Georg Thieme Verlag Stuttgart · New York

Palladium-Catalyzed Synthesis of Biaryl Ketones via tert-Butyl Isocyanide Insertion

Zhong Chen
College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)67166591   Email: zhuyongming@suda.edu.cn
,
Huaqing Duan
College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)67166591   Email: zhuyongming@suda.edu.cn
,
Xiao Jiang
College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)67166591   Email: zhuyongming@suda.edu.cn
,
Jinmei Wang
College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)67166591   Email: zhuyongming@suda.edu.cn
,
Yongming Zhu*
College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)67166591   Email: zhuyongming@suda.edu.cn
,
Shilin Yang
College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, P. R. of China   Fax: +86(512)67166591   Email: zhuyongming@suda.edu.cn
› Author Affiliations
Further Information

Publication History

Received: 26 February 2014

Accepted after revision: 25 March 2014

Publication Date:
08 May 2014 (online)


Abstract

A simple and efficient palladium-catalyzed carbonylative Suzuki coupling via tert-butyl isocyanide insertion has been developed, which demonstrates the utility of isocyanides in intermolecular C–C bond construction. This methodology provides a novel pathway for the synthesis of diaryl ketones in moderate to good yields. The approach is tolerant to a wide range of substrates and applicable to library synthesis. A possible reaction mechanism was proposed based on the experimental results.

Supporting Information