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Cu(OAc)2-catalyzed three-component cycloaddition of malonates, nitrosoarenes and alkenes: access to isoxazolidines.
Wu, Yuting; Liu, Qiang; Huang, Shuangping; Zhang, Chaofeng; Wei, Wenlong; Li, Xing.
Afiliação
  • Wu Y; College of Biomedical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan 030024, China. lixing@tyut.edu.cn.
  • Liu Q; College of Biomedical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan 030024, China. lixing@tyut.edu.cn.
  • Huang S; College of Biomedical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan 030024, China. lixing@tyut.edu.cn.
  • Zhang C; College of Biomedical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan 030024, China. lixing@tyut.edu.cn.
  • Wei W; College of Biomedical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan 030024, China. lixing@tyut.edu.cn.
  • Li X; College of Biomedical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan 030024, China. lixing@tyut.edu.cn.
Org Biomol Chem ; 21(17): 3669-3674, 2023 May 03.
Article em En | MEDLINE | ID: mdl-37067779
ABSTRACT
The Cu(OAc)2-catalyzed one-pot three-component cycloaddition of malonates, nitrosoarenes and alkenes is described. A wide range of isoxazolidines could be obtained in moderate to excellent yields via this method. Mechanistic investigations indicated that the key step in this catalytic system is the straightforward formation of nitrone intermediates through the Cu(OAc)2-catalyzed reaction of malonates with nitrosoarenes.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article