Issue 12, 2022

Visible light-induced N-radical 5-exo/6-endo cyclization of alkenyl amides: facile access to isoindolinones/isoquinolinones

Abstract

An efficient N-centered radical intramolecular cyclization reaction of alkenyl amides induced by visible light was described. In this process, an alkenyl amide underwent 5-exo/6-endo cyclization to selectively yield two critical alkaloid structures, namely isoindolinones and isoquinolinones.

Graphical abstract: Visible light-induced N-radical 5-exo/6-endo cyclization of alkenyl amides: facile access to isoindolinones/isoquinolinones

Supplementary files

Article information

Article type
Communication
Submitted
15 Feb 2022
Accepted
02 Mar 2022
First published
03 Mar 2022

Org. Biomol. Chem., 2022,20, 2397-2401

Visible light-induced N-radical 5-exo/6-endo cyclization of alkenyl amides: facile access to isoindolinones/isoquinolinones

Z. Lei, K. Hu, Y. He, S. Geng, L. Chen, S. Zou, L. Pan, Z. Ding and F. Huang, Org. Biomol. Chem., 2022, 20, 2397 DOI: 10.1039/D2OB00317A

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