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C-C Bond Cleavage Mediated Reaction for Constructing 3-Carbonyl Imidazo[1,5-a] Pyridines from 1,3-Dicarbonyl Compounds and Pyridin-2-ylmethanamines.
Wang, Qiang; Yao, Xia; Zhao, Peilan; Liu, Wanxiang; Zhao, Wangyan; Fang, Xin; Zhu, Yun; Dai, Gangqiang.
Afiliación
  • Wang Q; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
  • Yao X; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
  • Zhao P; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
  • Liu W; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
  • Zhao W; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
  • Fang X; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
  • Zhu Y; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
  • Dai G; College of life and Health Sciences, Anhui Science and Technology University, Fengyang 233100, P. R. China.
J Org Chem ; 88(19): 14193-14199, 2023 Oct 06.
Article en En | MEDLINE | ID: mdl-37696811
A [4 + 1] cyclization and C-C bond cleavage process mediated reaction for constructing 3-carbonyl imidazo[1,5-a] pyridines from 1,3-dicarbonyl compounds and pyridin-2-ylmethanamines has been developed. Various 1,3-dicarbonyl compounds are applicable, and selectivity could be achieved. Importantly, this strategy could be extended to an atom economy method by employing a cyclic 1,3-dicarbonyl compound, and it provided a new view for C-C bond cleavage reactions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos