Issue 11, 2015

Direct radical trifluoromethylthiolation and thiocyanation of aryl alkynoate esters: mild and facile synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins

Abstract

A mild and convenient oxidative radical cyclization of aryl alkynoate esters for the synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins has been developed using AgSCF3 and AgSCN as the corresponding radical sources, respectively. This protocol is characterized by readily available starting materials, excellent functional group tolerance and good yields.

Graphical abstract: Direct radical trifluoromethylthiolation and thiocyanation of aryl alkynoate esters: mild and facile synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins

Supplementary files

Article information

Article type
Research Article
Submitted
27 Aug 2015
Accepted
15 Sep 2015
First published
16 Sep 2015

Org. Chem. Front., 2015,2, 1511-1515

Author version available

Direct radical trifluoromethylthiolation and thiocyanation of aryl alkynoate esters: mild and facile synthesis of 3-trifluoromethylthiolated and 3-thiocyanated coumarins

Y. Zeng, D. Tan, Y. Chen, W. Lv, X. Liu, Q. Li and H. Wang, Org. Chem. Front., 2015, 2, 1511 DOI: 10.1039/C5QO00271K

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