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

Autoren

  • 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
Weitere Informationen

Publikationsverlauf

Received: 24. März 2016

Accepted after revision: 21. Mai 2016

Publikationsdatum:
21. Juni 2016 (online)


Graphical Abstract

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