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Electrochemical Radical Reaction Construction of C-C Bonds: Access to 1,4-Dicarbonyl Compounds from Enol Acetates and 1,3-Diketones.
Wu, Fan; Liu, Shengjun; Lv, Xiaoqing; Pan, Mei; Liu, Xiaoqin; Zhang, Jinpeng; Rong, Liangce.
Afiliação
  • Wu F; School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
  • Liu S; School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
  • Lv X; School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
  • Pan M; School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
  • Liu X; School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
  • Zhang J; Key Lab of Environment and Health, School of Public Health, Xuzhou Medical University, Xuzhou 221004, Jiangsu, P. R. China.
  • Rong L; School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
J Org Chem ; 88(19): 13749-13759, 2023 Oct 06.
Article em En | MEDLINE | ID: mdl-37726915
ABSTRACT
As important substrates for the construction of heterocycles, a simple and efficient approach for synthesis of 1,4-diones is highly desirable. In this work, novel and efficient electrochemical radical reactions of enol acetates and 1,3-diketones have been developed to successfully achieve 1,4-diketones under catalyst-free and oxidant-free conditions. The wide range of substrates, good group tolerance, and simple operation process make the approach have important practical value. Moreover, the obtained 1,4-diketones can be easily further transformed to pyrrole and furan derivatives.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article