Visible-light–enabled reduction of arylsulfonyl and benzoyl azides to access primary arylsulfonamides and benzoyl amides

Abstract

Photocatalyzed reduction of arylsulfonyl and benzoyl azides, which could serve as temporary masking groups for amides, was achieved to access primary sulfonamides and benzoyl amides in mild conditions using organic reductant. A wide range of structurally diverse arylsulfonamides and benzoyl amides were accessed in good yields using this protocol. The mechanistic pathway of this reaction might generate the key amidyl radical through single-electron transfer (SET).

Graphical abstract: Visible-light–enabled reduction of arylsulfonyl and benzoyl azides to access primary arylsulfonamides and benzoyl amides

Supplementary files

Article information

Article type
Communication
Submitted
29 Apr 2025
Accepted
07 Jul 2025
First published
08 Jul 2025

Chem. Commun., 2025, Advance Article

Visible-light–enabled reduction of arylsulfonyl and benzoyl azides to access primary arylsulfonamides and benzoyl amides

Q. Li, X. Ma, Y. Bi, M. Ma, P. Zhang and X. Sui, Chem. Commun., 2025, Advance Article , DOI: 10.1039/D5CC02400E

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