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Regio- and stereoselective syntheses of chiral α-quaternary (Z)-trisubstituted allylic amino acids via synergistic Pd/Cu catalysis.
Ke, Miaolin; Yu, Yuyan; Sun, Longwu; Li, Xinzhi; Cao, Qianqian; Xiao, Xiao; Chen, Fener.
Afiliação
  • Ke M; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. pharmxiao@zjut.edu.cn.
  • Yu Y; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. pharmxiao@zjut.edu.cn.
  • Sun L; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. pharmxiao@zjut.edu.cn.
  • Li X; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. pharmxiao@zjut.edu.cn.
  • Cao Q; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. pharmxiao@zjut.edu.cn.
  • Xiao X; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. pharmxiao@zjut.edu.cn.
  • Chen F; Institute of Pharmaceutical Science and Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. pharmxiao@zjut.edu.cn.
Chem Commun (Camb) ; 59(18): 2632-2635, 2023 Feb 28.
Article em En | MEDLINE | ID: mdl-36779224
ABSTRACT
Synergistic palladium/copper catalysis for asymmetric allylic alkylation of vinylethylene carbonates with aldimine esters has been developed for the synthesis of α-quaternary (Z)-trisubstituted allylic amino acids under mild conditions. This methodology features broad substrate compatibilities in yields of up to 87% and up to 94% ee. A facile scale-up and straightforward conversion to 1,2,3,5-tetrasubstituted pyrrole and 1,2,5,6-tetrahydropyridine bearing chiral quaternary carbon centers verifies the synthetic utility of this method.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article