Issue 11, 2022

Photoinduced aerobic C–S borylation of aryl sulfides

Abstract

Direct C–S borylation of aryl sulfides with B2pin2 has been achieved via a transition-metal-free photochemical process. Under blue LED irradiation, aryl sulfides with various functional groups were converted to aryl boronate esters under ambient conditions using 1,4-benzoquinone as the photosensitizer. This transformation provides an opportunity to transform the widely existing alkylthio group to a convertible group for applications in organic synthesis.

Graphical abstract: Photoinduced aerobic C–S borylation of aryl sulfides

Supplementary files

Article information

Article type
Research Article
Submitted
13 Feb 2022
Accepted
14 Apr 2022
First published
16 Apr 2022

Org. Chem. Front., 2022,9, 3034-3038

Photoinduced aerobic C–S borylation of aryl sulfides

X. Li, Z. Wan, X. Hu and H. Zhang, Org. Chem. Front., 2022, 9, 3034 DOI: 10.1039/D2QO00240J

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