Issue 61, 2024

Photoinduced EnT-mediated sulfonamidylimination of alkenes and (hetero)arenes with iminophenylacetic acid oxime esters

Abstract

A photoinduced EnT-mediated generation of sulfonamidyl radicals has been accomplished using rationally designed iminophenylacetic acid oxime ester reagents under metal-free conditions. This approach offers a mild, regio- and diastereoselective synthesis of N-sulfonyl diamines via diamination of alkenes and (hetero)arenes.

Graphical abstract: Photoinduced EnT-mediated sulfonamidylimination of alkenes and (hetero)arenes with iminophenylacetic acid oxime esters

Supplementary files

Article information

Article type
Communication
Submitted
08 May 2024
Accepted
25 Jun 2024
First published
26 Jun 2024

Chem. Commun., 2024,60, 7934-7937

Photoinduced EnT-mediated sulfonamidylimination of alkenes and (hetero)arenes with iminophenylacetic acid oxime esters

Z. Sun, J. Zhang, X. Du, L. Liu, S. Gao, C. Qi, X. Li and X. Xu, Chem. Commun., 2024, 60, 7934 DOI: 10.1039/D4CC02225D

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