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Copper-catalyzed intramolecular dearomative aza-Wacker reaction of indole.
Wang, Bi; Liang, Ren-Xiao; Shen, Zhen-Lu; Jia, Yi-Xia.
Afiliación
  • Wang B; College of Chemical Engineering, State Key Laboratory Breeding Base of Green Chemical Synthesis Technology, Zhejiang University of Technology, Chaowang Road #18, Hangzhou 310014, China. zhenlushen@zjut.edu.cn.
  • Liang RX; College of Chemical Engineering, State Key Laboratory Breeding Base of Green Chemical Synthesis Technology, Zhejiang University of Technology, Chaowang Road #18, Hangzhou 310014, China. zhenlushen@zjut.edu.cn.
  • Shen ZL; College of Chemical Engineering, State Key Laboratory Breeding Base of Green Chemical Synthesis Technology, Zhejiang University of Technology, Chaowang Road #18, Hangzhou 310014, China. zhenlushen@zjut.edu.cn.
  • Jia YX; College of Chemical Engineering, State Key Laboratory Breeding Base of Green Chemical Synthesis Technology, Zhejiang University of Technology, Chaowang Road #18, Hangzhou 310014, China. zhenlushen@zjut.edu.cn.
Chem Commun (Camb) ; 60(28): 3858-3861, 2024 Apr 02.
Article en En | MEDLINE | ID: mdl-38497365
ABSTRACT
Herein, we describe a copper-catalyzed intramolecular dearomative amination of indoles via a formal aza-Wacker reaction. This protocol provides an efficient method to access aza-polycyclic indoline molecules bearing exocyclic CC bonds in moderate to excellent yields in the presence of molecular oxygen as an oxidant. It is worth noting that indolin-3-ones are achieved when employing C3-non-substituted indoles as substrates.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China
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