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Ru(II)-Catalyzed Divergent C-H Alkynylation Cascade with Bifunctional α-Alcohol Haloalkynes.
Zhang, Qiaoya; Li, Yinling; Chen, Yabo; Jiang, Jiahua; Liu, Yuan; Luo, Jiye; Gao, Yang; Huo, Yanping; Chen, Qian; Li, Xianwei.
Afiliação
  • Zhang Q; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Li Y; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Chen Y; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Jiang J; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Liu Y; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Luo J; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Gao Y; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Huo Y; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Chen Q; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
  • Li X; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
Org Lett ; 26(11): 2186-2191, 2024 Mar 22.
Article em En | MEDLINE | ID: mdl-38452270
ABSTRACT
Native functionality directed the C-H activation cascade to enable rapid construction of molecular complexity, featuring step-economy and synthetic efficiency. Herein, by exploiting bifunctional α-alcohol haloalkynes, we developed Ru(II)-catalyzed carboxylic acid, amine, and amide assisted divergent C-H alkynylation and annulation cascade, affording polyfunctional heterocycles. Significantly, a bilateral aryl C-H polycyclization cascade of azobenzenes was achieved using the versatile haloalkynes.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China