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Synthesis of 1,2,4,5-tetra-substituted benzenes via copper-catalyzed dimerization of γ,δ-unsaturated ketones.
Ma, Kai-Xian; Hong, Chuan-Ming; Yan, Jiang-Min; Li, Qing-Hua; Liu, Tang-Lin.
Afiliação
  • Ma KX; Chongqing Key Laboratory of Soft-Matter Materials Manufacturing, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China. liuschop@swu.edu.cn.
  • Hong CM; Chongqing Key Laboratory of Soft-Matter Materials Manufacturing, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China. liuschop@swu.edu.cn.
  • Yan JM; Chongqing Key Laboratory of Soft-Matter Materials Manufacturing, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China. liuschop@swu.edu.cn.
  • Li QH; Chongqing Key Laboratory of Soft-Matter Materials Manufacturing, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China. liuschop@swu.edu.cn.
  • Liu TL; Chongqing Key Laboratory of Soft-Matter Materials Manufacturing, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China. liuschop@swu.edu.cn.
Chem Commun (Camb) ; 60(60): 7753-7756, 2024 Jul 23.
Article em En | MEDLINE | ID: mdl-38973629
ABSTRACT
An efficient cyclization for the synthesis of 1,2,4,5-tetra-substituted benzenes via copper catalyzed dimerization of γ,δ-unsaturated ketones has been described. This one-pot procedure employs the γ,δ-unsaturated ketones as the sole substrate with multiple C-C bond formation. This protocol features broad substrate scope and provides a facile and robust method to construct polysubstituted benzene derivatives under mild conditions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China