Issue 83, 2024

Deoxygenation of allyl arylsulfones to allyl arylthioethers via a “cut-sew” strategy: phosphines as bifunctional reagents

Abstract

Herein, we disclosed a protocol for the deoxygenation of allyl arylsulfones to access the corresponding thioethers under photoredox conditions by a “cut-sew” strategy. The key to the success of the deoxygenation process is using triarylphosphines not only as the terminal reductants, but also as the reaction initiators. Deeper understanding of this deoxygenation process enabled the intermolecular deoxygenative allylation.

Graphical abstract: Deoxygenation of allyl arylsulfones to allyl arylthioethers via a “cut-sew” strategy: phosphines as bifunctional reagents

Supplementary files

Article information

Article type
Communication
Submitted
17 Aug 2024
Accepted
24 Sep 2024
First published
25 Sep 2024

Chem. Commun., 2024,60, 11996-11999

Deoxygenation of allyl arylsulfones to allyl arylthioethers via a “cut-sew” strategy: phosphines as bifunctional reagents

L. Dong, T. Shu, D. Yang and M. Chen, Chem. Commun., 2024, 60, 11996 DOI: 10.1039/D4CC04199B

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