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Copper-catalyzed atroposelective formal [4+1] annulation of 1,2-diketones with vinyl cations.
Wang, Ze-Shu; Xu, Hao-Jin; Chen, Yang-Bo; Ye, Long-Wu; Zhou, Bo; Qian, Peng-Cheng.
Afiliação
  • Wang ZS; Institute of New Materials & Industry Technology, College of Chemistry & Materials Engineering, Wenzhou University, Wenzhou 325035, China. qpc@wzu.edu.cn.
  • Xu HJ; Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China. longwuye@xmu.edu.cn.
  • Chen YB; Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China. longwuye@xmu.edu.cn.
  • Ye LW; Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China. longwuye@xmu.edu.cn.
  • Zhou B; Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China. longwuye@xmu.edu.cn.
  • Qian PC; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China.
Chem Commun (Camb) ; 59(100): 14831-14834, 2023 Dec 14.
Article em En | MEDLINE | ID: mdl-38013471
The enantioselective transformation of easily accessible 1,2-diketones represents a quick pathway towards enantioenriched molecules. Herein, we disclose a copper-catalyzed atroposelective formal [4+1] annulation of 1,2-diketones with vinyl cations, enabling the efficient and atom-economical construction of axially chiral arylpyrroles bearing 1,3-dioxole moieties with good to excellent enantioselectivities under mild reaction conditions. Importantly, this methodology constitutes the first enantioselective formal [4+1] annulation of 1,2-diketones.

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