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Diastereo- and enantioselective synthesis of biaryl aldehydes bearing both axial and central chirality.
Huang, Fen; Tao, Ling-Fei; Liu, Jiyong; Qian, Linghui; Liao, Jia-Yu.
Afiliación
  • Huang F; College of Pharmaceutical Sciences, and Hangzhou Institute of Innovative Medicine, Zhejiang University, Hangzhou 310058, China. lhqian@zju.edu.cn.
  • Tao LF; College of Pharmaceutical Sciences, and Hangzhou Institute of Innovative Medicine, Zhejiang University, Hangzhou 310058, China. lhqian@zju.edu.cn.
  • Liu J; Department of Chemistry, Zhejiang University, Hangzhou 310058, China.
  • Qian L; College of Pharmaceutical Sciences, and Hangzhou Institute of Innovative Medicine, Zhejiang University, Hangzhou 310058, China. lhqian@zju.edu.cn.
  • Liao JY; College of Pharmaceutical Sciences, and Hangzhou Institute of Innovative Medicine, Zhejiang University, Hangzhou 310058, China. lhqian@zju.edu.cn.
Chem Commun (Camb) ; 59(30): 4487-4490, 2023 Apr 11.
Article en En | MEDLINE | ID: mdl-36971075
We describe herein an intriguing method for the synthesis of biaryl aldehydes bearing both axial and central chirality through a desymmetric [3 + 2] cycloaddition reaction of activated isocyanides with prochiral biaryl dialdehydes under silver catalysis. This protocol features excellent enantioselectivity, 100% atom economy, good functional group compatibility, and operational simplicity.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido