Synlett 2016; 27(15): 2264-2268
DOI: 10.1055/s-0035-1562494
letter
© Georg Thieme Verlag Stuttgart · New York

Copper-Catalyzed Regioselective Sulfenylation of Thiazolo[3,2-b]-1,2,4-triazoles with Thiols

Shaohua Wang
School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou 510006, P. R. of China   Email: wjliu1113@126.com
,
Wenjie Liu*
School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou 510006, P. R. of China   Email: wjliu1113@126.com
,
Zhihao Cai
School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou 510006, P. R. of China   Email: wjliu1113@126.com
,
Shenghao Li
School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou 510006, P. R. of China   Email: wjliu1113@126.com
,
Jianwen Liu
School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou 510006, P. R. of China   Email: wjliu1113@126.com
,
Anda Wang
School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou 510006, P. R. of China   Email: wjliu1113@126.com
› Author Affiliations
Further Information

Publication History

Received: 24 March 2016

Accepted after revision: 21 May 2016

Publication Date:
21 June 2016 (online)


Abstract

A simple and useful protocol was developed for the regioselective copper-catalyzed direct sulfenylation of thiazolo[3,2-b]-1,2,4-triazoles with thiols. The reaction shows broad functional-group tolerance and provides rapid access to sulfenylated thiazolo[3,2-b]-1,2,4-triazoles in moderate to good yields.

Supporting Information

 
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