Erythrosine B Catalyzed Visible‐Light Photoredox Arylation–Cyclization of  N ‐Alkyl‐ N ‐aryl‐2‐(trifluoromethyl)acrylamides to 3‐(Trifluoromethyl)indolin‐2‐one Derivatives | Zendy

Gonda Zsombor | Zendy; Béke Ferenc | Zendy; Tischler Orsolya | Zendy; Petró Milán | Zendy; Novák Zoltán | Zendy; Tóth Balázs L. | Zendy

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Erythrosine B Catalyzed Visible‐Light Photoredox Arylation–Cyclization of N ‐Alkyl‐ N ‐aryl‐2‐(trifluoromethyl)acrylamides to 3‐(Trifluoromethyl)indolin‐2‐one Derivatives

Author(s) -

Gonda Zsombor,

Béke Ferenc,

Tischler Orsolya,

Petró Milán,

Novák Zoltán,

Tóth Balázs L.

Publication year - 2017

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201601493

Subject(s) - chemistry , trifluoromethyl , aryl , alkyl , photocatalysis , erythrosine , medicinal chemistry , visible spectrum , catalysis , photochemistry , organic chemistry , physics , optoelectronics

3‐Trifluoromethylindoline‐2‐one derivatives were prepared in a visible‐light photocatalytic transformation of acrylamides. The arylation–cyclization sequence was initiated by light‐induced aryl radical generation from aryldiazonium salts with the utilization of erythrosine B as an organic photocatalyst.

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