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Iridium-catalyzed asymmetric cascade dearomative allylation/acyl transfer rearrangement: access to chiral N-substituted 2-pyridones.
Wang, Wei-Yi; Yi, Zhi-Yuan; Wang, Zuo-Fei; Dong, Xiu-Qin; Wang, Chun-Jiang.
Afiliação
  • Wang WY; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, 430072, P. R. China. cjwang@whu.edu.cn.
  • Yi ZY; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, 430072, P. R. China. cjwang@whu.edu.cn.
  • Wang ZF; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, 430072, P. R. China. cjwang@whu.edu.cn.
  • Dong XQ; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, 430072, P. R. China. cjwang@whu.edu.cn.
  • Wang CJ; College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, 430072, P. R. China. cjwang@whu.edu.cn.
Chem Commun (Camb) ; 60(38): 5086-5089, 2024 May 07.
Article em En | MEDLINE | ID: mdl-38639097
ABSTRACT
Iridium-catalyzed dearomative allylation/acyl transfer rearrangement has been developed using easily available 2-pyridinyl benzoates and vinyl ethylene carbonate. This protocol enabled the expedient synthesis of a variety of chiral N-substituted 2-pyridones in good to high yields with excellent enantioselectivity. It has the advantages of high atom economy, wide substrate scope, gram-scale synthesis, and versatile synthetic transformations.

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