Synthesis of indolines via palladium-catalyzed [4 + 1] annulation of (2-aminophenyl)methanols with sulfoxonium ylides

A facile strategy for the synthesis of valuable indolines has been developed, involving a palladium(II)/Brønsted acid co-catalyzed annulation of readily available (2-aminophenyl)methanols and sulfoxonium ylides. This protocol allows for the direct utilization of the OH group as a leaving group, tole...

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Veröffentlicht in:Organic & biomolecular chemistry 2024-08, Vol.22 (31), p.6342-6351
Hauptverfasser: Hao, Erxiao, Kong, Xiaomei, Xu, Tongyu, Zeng, Fanlong
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Sprache:eng
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Zusammenfassung:A facile strategy for the synthesis of valuable indolines has been developed, involving a palladium(II)/Brønsted acid co-catalyzed annulation of readily available (2-aminophenyl)methanols and sulfoxonium ylides. This protocol allows for the direct utilization of the OH group as a leaving group, tolerates alkyl and aryl groups on the N atom of the aniline moiety, operates under mild reaction conditions, and exhibits good efficiency.
ISSN:1477-0520
1477-0539
DOI:10.1039/d4ob00983e