Issue 48, 2022

Visible-light-promoted radical cascade alkylation/cyclization: access to alkylated indolo/benzoimidazo[2,1-a]isoquinolin-6(5H)-ones

Abstract

A new protocol is herein described for the direct generation of alkylated indolo/benzoimidazo[2,1-a]isoquinolin-6(5H)-one derivatives by using Hantzsch esters as alkylation radical precursors using a photoredox/K2S2O8 system. This oxidative alkylation of active alkenes involves a radical cascade cyclization process and a sequence of Hantzsch ester single electron oxidation, C–C bond cleavage, alkylation, arylation and oxidative deprotonation.

Graphical abstract: Visible-light-promoted radical cascade alkylation/cyclization: access to alkylated indolo/benzoimidazo[2,1-a]isoquinolin-6(5H)-ones

Supplementary files

Article information

Article type
Paper
Submitted
22 Sep 2022
Accepted
15 Nov 2022
First published
16 Nov 2022

Org. Biomol. Chem., 2022,20, 9659-9671

Visible-light-promoted radical cascade alkylation/cyclization: access to alkylated indolo/benzoimidazo[2,1-a]isoquinolin-6(5H)-ones

W. Yu, B. Xiong, L. Zhong and Y. Liu, Org. Biomol. Chem., 2022, 20, 9659 DOI: 10.1039/D2OB01732F

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