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Catalytic asymmetric construction of helicenes via transformation of biaryls.
Fan, Peiling; Li, Lun; Qian, Deyun.
Afiliação
  • Fan P; Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Key Laboratory of Research and Development for Natural Products, School of Pharmacy, Yunnan University, Kunming 650500, P.R. China. dyqian@ynu.edu.cn.
  • Li L; School of Chemical Science and Technology, Yunnan University, Kunming 650500, P.R. China.
  • Qian D; Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Key Laboratory of Research and Development for Natural Products, School of Pharmacy, Yunnan University, Kunming 650500, P.R. China. dyqian@ynu.edu.cn.
Org Biomol Chem ; 22(16): 3186-3197, 2024 Apr 24.
Article em En | MEDLINE | ID: mdl-38591656
ABSTRACT
This review showcases a systematic overview of the available tools for the catalytic asymmetric transformation of biaryl substrates toward the construction of challenging enantioenriched helicenes and the conceptual aspects associated with each type of transformation. Depending on the properties of the biaryl and the nature of the process, several methodologies have been developed, including olefin metathesis, hydroarylation of alkynes, C-X (X = C, O, N) coupling, and C-H functionalization. Pioneering studies and an array of representative reactions are discussed to underscore the potential of these synthetic protocols.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article