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Mendeleev Communications, 2025, Volume 35, Issue 6, Pages 717–719
DOI: https://doi.org/10.71267/mencom.7798
(Mi mendc7327)
 

Communications

Photocatalytic radical arylation/cyclization of N-arylacrylamides to 3-benzyl oxindoles

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

a Department of Chemical and Material Engineering, Quzhou College of Technology, 324002 Quzhou, P. R. China
b College of Chemical Engineering, Nanjing Forestry University, 210037 Nanjing, P. R. China
c School of Chemical and Pharmaceutical Engineering, Changzhou Vocational Institute of Engineering, 213164 Changzhou, P. R. China
References:
Abstract: A photocatalytic tandem radical arylation/cyclization of N-arylacrylamides with diaryliodonium triflates at room temperature affords 3-(benzyl)oxindoles in moderate to good yields. The diaryliodonium triflates upon blue visible light irradiation in the presence of Ir(ppy)2(dtbbpy) · PF6 as the photocatalyst release aryl radicals which would add at the double bond of the acrylamide to initiate the cyclization involving the N-aryl substituent.
Keywords: photocatalysis, arylation, diaryliodonium triflate, arylacrylamides, radical cyclization, oxindoles.
Received: 10.04.2025
Accepted: 28.05.2025
Published: 21.10.2025
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (5.1 Mb)


Citation: J. Wang, W. Lai, M. Hong, Ch. Liu, L. Wang, “Photocatalytic radical arylation/cyclization of N-arylacrylamides to 3-benzyl oxindoles”, Mendeleev Commun., 35:6 (2025), 717–719
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