Issue 17, 2024

Photoinduced decatungstate-catalyzed C(sp3)–H thioetherification by sulfinate salts

Abstract

Thiols and thioesters play crucial roles in pharmaceuticals, biology, and material science as essential organosulfur compounds. Leveraging readily available and cost-effective inert alkanes through direct thioetherification holds promise for yielding high-value-added products. Herein, we present a photoinduced strategy for sulfur-containing modification of inert alkanes utilizing decatungstate as hydrogen atom transfer reagent, offering a straightforward and practical approach for synthesizing thioethers and thioesters.

Graphical abstract: Photoinduced decatungstate-catalyzed C(sp3)–H thioetherification by sulfinate salts

Supplementary files

Article information

Article type
Paper
Submitted
10 Mar 2024
Accepted
02 Apr 2024
First published
03 Apr 2024

Org. Biomol. Chem., 2024,22, 3420-3424

Photoinduced decatungstate-catalyzed C(sp3)–H thioetherification by sulfinate salts

P. Li, J. Tu, A. Hu, L. Guo, C. Yang and W. Xia, Org. Biomol. Chem., 2024, 22, 3420 DOI: 10.1039/D4OB00394B

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