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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2025 Volume 35, Issue 6, Pages 717–719 (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

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

Language: English

DOI: 10.71267/mencom.7798



© Steklov Math. Inst. of RAS, 2025