Issue 4, 2025

Visible-light-induced cascade radical cyclization to access sulfamoylated benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-ones

Abstract

We report, for the first time, a visible-light-induced cascade radical sulfamoylation and cyclization of 2-arylbenzoimidazoles using sulfamoyl chlorides as sulfamoylation reagents to access sulfamoylated benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-ones. The readily available nature of sulfamoyl chlorides and the metal-free conditions make this method a promising strategy for the synthesis of these compounds.

Graphical abstract: Visible-light-induced cascade radical cyclization to access sulfamoylated benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-ones

Supplementary files

Article information

Article type
Paper
Submitted
09 Қар. 2024
Accepted
30 Қар. 2024
First published
03 Жел. 2024

Org. Biomol. Chem., 2025,23, 892-899

Visible-light-induced cascade radical cyclization to access sulfamoylated benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-ones

R. Huang, W. Wang, K. Lu and X. Zhao, Org. Biomol. Chem., 2025, 23, 892 DOI: 10.1039/D4OB01809E

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