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Accessing pyrrolo[1,2-a]indole derivatives via visible-light-induced dearomatizative cyclization of indoles.
Liu, Zhaosheng; Ji, Xiaochen; Duan, Lilan; Deng, Guo-Jun; Huang, Huawen.
Afiliación
  • Liu Z; College of Chemistry, Xiangtan University, Xiangtan 411105, China. xcji@xtu.edu.cn.
  • Ji X; College of Chemistry, Xiangtan University, Xiangtan 411105, China. xcji@xtu.edu.cn.
  • Duan L; College of Chemistry, Xiangtan University, Xiangtan 411105, China. xcji@xtu.edu.cn.
  • Deng GJ; College of Chemistry, Xiangtan University, Xiangtan 411105, China. xcji@xtu.edu.cn.
  • Huang H; School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, 453007, China.
Chem Commun (Camb) ; 60(37): 4902-4905, 2024 May 02.
Article en En | MEDLINE | ID: mdl-38619574
ABSTRACT
Pyrrolo[1,2-a]indoles are structurally important scaffolds in many natural products and bioactive compounds. Herein, we report a novel synthetic method for pyrrolo[1,2-a]indole derivatives through visible-light-induced cascade dearomatizative cyclization of indoles with external nucleophiles. Moderate yields, good diastereoselectivities, and excellent regioselectivities were generally observed with the resultant indole-fused polycyclic compounds.

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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