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Visible-Light-Mediated Ipso-Carboacylation of Alkynes: Synthesis of 3-Acylspiro[4,5]trienones from N-(p-Methoxyaryl)propiolamides and Acyl Chlorides.
Liu, Yu; Wang, Qiao-Lin; Zhou, Cong-Shan; Xiong, Bi-Quan; Zhang, Pan-Liang; Yang, Chang-An; Tang, Ke-Wen.
Afiliação
  • Liu Y; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology , Yueyang 414006, China.
  • Wang QL; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology , Yueyang 414006, China.
  • Zhou CS; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology , Yueyang 414006, China.
  • Xiong BQ; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology , Yueyang 414006, China.
  • Zhang PL; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology , Yueyang 414006, China.
  • Yang CA; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology , Yueyang 414006, China.
  • Tang KW; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology , Yueyang 414006, China.
J Org Chem ; 83(4): 2210-2218, 2018 02 16.
Article em En | MEDLINE | ID: mdl-29341610
ABSTRACT
A novel visible-light-mediated ipso-carboacylation of N-(p-methoxyaryl)propiolamides with acyl chloride has been established for the synthesis of diverse 3-acylspiro[4,5]trienones with high selectivity and efficiency. This method represents a new difunctionalization of alkynes through cross coupling of the acyl chloride C-Cl bonds with an ipso-aromatic carbon by simultaneously forming two new carbon-carbon bonds and one carbon-oxygen double bond.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China