Issue 14, 2019

Metal- and phosphine-free electrophilic vicinal chloro-alkylthiolation and trifluoromethylthiolation of indoles using sodium sulfinate in the presence of triphosgene

Abstract

Efficient chloro-alkylthiolation and trifluoromethylthiolation of indole derivatives were developed. Triphosgene was used as a reducing agent for the first time to convert sodium sulfinate to highly active electrophilic intermediates (CH3SCl and CF3SOCl). This strategy involves the use of cheap and readily available reagents and has broad substrate scope.

Graphical abstract: Metal- and phosphine-free electrophilic vicinal chloro-alkylthiolation and trifluoromethylthiolation of indoles using sodium sulfinate in the presence of triphosgene

Supplementary files

Article information

Article type
Research Article
Submitted
12 Mar 2019
Accepted
08 Apr 2019
First published
20 May 2019

Org. Chem. Front., 2019,6, 2435-2440

Metal- and phosphine-free electrophilic vicinal chloro-alkylthiolation and trifluoromethylthiolation of indoles using sodium sulfinate in the presence of triphosgene

X. He, S. Majumder, J. Wu, C. Jin, S. Guo, Z. Guo and M. Yang, Org. Chem. Front., 2019, 6, 2435 DOI: 10.1039/C9QO00350A

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