RUS  ENG
Полная версия
ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2024, том 34, выпуск 6, страницы 834–836 (Mi mendc266)

Communications

Photocatalytic intramolecular carboazidation of N-arylacrylamides into 3-(azidomethyl)indolin-2-ones

J. Wanga, M. Hongb, Ch. Liuc, L. Wangc

a Quzhou College of Technology, Quzhou, P.R. China
b Nanjing Forestry University, Nanjing, P. R. China
c School of Chemical and Pharmaceutical Engineering, Changzhou Vocational Institute of Engineering, Changzhou, P.R. China


Аннотация: Intramolecular carboazidation of N-arylacrylamides with 1-azido-1λ3-benzo[d][1,2]iodaoxol-3(1H)-one (the N3-Togni reagent) affording 3-(azidomethyl)indolin-2-ones proceeds at room temperature under visible light irradiation with 2,4,5,6-tetra(carbazol-9-yl)-1,3-dicyanobenzene assistance. The latter provides the formation of azido radicals from the N3-Togni reagent. The investigated substrate scope involves 12 examples.

Ключевые слова: carboazidation, arylacrylamides, indolin-2-ones, radical cyclization, N3-Togni reagent, photocatalysis.

Язык публикации: английский

DOI: 10.1016/j.mencom.2024.10.021



© МИАН, 2025