Photoinduced halogen-bonding enabled synthesis of oxindoles and isoindolinones from aryl iodides

Org Biomol Chem. 2023 Jan 25;21(4):715-718. doi: 10.1039/d2ob01818g.

Abstract

We report the use of halogen bonding (XB) for the generation of aryl radicals from aryl halides under blue light irradiation and applied it in radical generation/1,5-hydrogen-atom transfer/radical cyclization cascade reactions for the synthesis of oxindoles and isoindolinones. On the basis of experimental studies, we propose that DBU can serve as a suitable XB acceptor with aryl halides for the formation of a photoactive electron donor and acceptor complex.