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
16 ذو القعدة 1443
Accepted
11 ذو الحجة 1443
First published
13 ذو الحجة 1443

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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