Visible light-promoted difluoromethylthiolation of aryldiazonium salts†
Abstract
Difluoromethylthiolation of aryldiazonium salts under photocatalytic conditions with a shelf-stable, easily prepared and inexpensive reagent, PhSO2SCF2H was described. A variety of difluoromethylthioethers were obtained utilizing aryldiazonium salts containing different functional groups. Aryldiazonium salts with a heteroarene moiety were tolerated. Fluorescence quenching experiments indicated that both oxidative and reductive quenching cycles occurred during this process.
- This article is part of the themed collections: Synthetic methodology in OBC and Catalysis & biocatalysis in OBC