Issue 17, 2022

External oxidant-free and selective thiofunctionalization of alkenes enabled by photoredox-neutral catalysis

Abstract

A simple photoredox-neutral approach is reported for the three-component thiohydroxylation, thioalkoxylation and thioamination of vinylarenes towards valuable vicinal S,O- and S,N-disubstituted molecules. N-Phenyl-sulfenyl phthalimide, a commonly used sulfur electrophile, was herein demonstrated to act as a thiyl radical precursor and plays a crucial role in this reaction.

Graphical abstract: External oxidant-free and selective thiofunctionalization of alkenes enabled by photoredox-neutral catalysis

Supplementary files

Article information

Article type
Research Article
Submitted
15 juin 2022
Accepted
10 juil. 2022
First published
12 juil. 2022

Org. Chem. Front., 2022,9, 4536-4541

External oxidant-free and selective thiofunctionalization of alkenes enabled by photoredox-neutral catalysis

R. Liang, C. Zhu, P. Song, L. Zhao, Q. Tong and J. Zhong, Org. Chem. Front., 2022, 9, 4536 DOI: 10.1039/D2QO00957A

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