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Regioselective synthesis of N-containing polycyclic compounds via radical annulation cyclization of 1,7-dienes with aldehydes.
Sui, Jia-Li; Zhong, Long-Jin; Xiong, Bi-Quan; Tang, Ke-Wen; Liu, Yu.
Afiliação
  • Sui JL; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. zlj1511@hnu.edu.cn.
  • Zhong LJ; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. zlj1511@hnu.edu.cn.
  • Xiong BQ; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. zlj1511@hnu.edu.cn.
  • Tang KW; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. zlj1511@hnu.edu.cn.
  • Liu Y; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. zlj1511@hnu.edu.cn.
Chem Commun (Camb) ; 60(36): 4834-4837, 2024 Apr 30.
Article em En | MEDLINE | ID: mdl-38619398
ABSTRACT
A convenient method for oxidant-promoted radical cascade acylation or decarbonylative alkylation of 1,7-dienes with aldehydes has been established. This method allows for the rapid construction of N-containing polycyclic skeletons in a highly regio- and stereoselective manner. This transformation provides a simple and efficient method for the preparation of a range of tetrahydro-6H-indeno[2,1-c]quinolinone derivatives by sequential formation of three new carbon-carbon bonds. Additionally, this radical cascade cyclization can selectively convert aldehydes into aroyl/primary aliphatic acyl radicals and secondary or tertiary alkyl radicals.

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