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Synthesis of indolines via palladium-catalyzed [4 + 1] annulation of (2-aminophenyl)methanols with sulfoxonium ylides.
Hao, Erxiao; Kong, Xiaomei; Xu, Tongyu; Zeng, Fanlong.
Afiliação
  • Hao E; Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, National Demonstration Center for Experimental Chemistry Education, College of Chemistry & Materials Science, Northwest University, 1 Xuefu Road, Xi'an, Shaanxi, 710127, P. R. China. fzeng@nwu.edu.cn.
  • Kong X; Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, National Demonstration Center for Experimental Chemistry Education, College of Chemistry & Materials Science, Northwest University, 1 Xuefu Road, Xi'an, Shaanxi, 710127, P. R. China. fzeng@nwu.edu.cn.
  • Xu T; Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, National Demonstration Center for Experimental Chemistry Education, College of Chemistry & Materials Science, Northwest University, 1 Xuefu Road, Xi'an, Shaanxi, 710127, P. R. China. fzeng@nwu.edu.cn.
  • Zeng F; Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, National Demonstration Center for Experimental Chemistry Education, College of Chemistry & Materials Science, Northwest University, 1 Xuefu Road, Xi'an, Shaanxi, 710127, P. R. China. fzeng@nwu.edu.cn.
Org Biomol Chem ; 22(31): 6342-6351, 2024 Aug 07.
Article em En | MEDLINE | ID: mdl-39041823
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem / Org. biomol. chem / Organic & biomolecular chemistry Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem / Org. biomol. chem / Organic & biomolecular chemistry Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido