aQuzhou College of Technology, Quzhou, P.R. China bNanjing Forestry University, Nanjing, P. R. China cSchool 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.
Образец цитирования:
J. Wang, M. Hong, Ch. Liu, L. Wang, “Photocatalytic intramolecular carboazidation of N-arylacrylamides into 3-(azidomethyl)indolin-2-ones”, Mendeleev Commun., 34:6 (2024), 834–836
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