Issue 4, 2023

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

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.

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

Supplementary files

Article information

Article type
Communication
Submitted
05 Oct 2022
Accepted
16 Nov 2022
First published
17 Nov 2022

Org. Biomol. Chem., 2023,21, 715-718

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

W. Tang, K. Chen, D. Sun and X. Chen, Org. Biomol. Chem., 2023, 21, 715 DOI: 10.1039/D2OB01818G

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