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Paired Electrolysis-Enabled Arylation of Quinoxalin-2(1H)-ones.
Hou, Jia-Cheng; Jiang, Jun; Wen, Yan-Cui; Zeng, Yan-Yan; Lu, Yu-Han; Wang, Jia-Sheng; Ou, Li-Juan; He, Wei-Min.
Afiliação
  • Hou JC; School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China.
  • Jiang J; School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China.
  • Wen YC; School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China.
  • Zeng YY; School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China.
  • Lu YH; School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China.
  • Wang JS; School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China.
  • Ou LJ; School of Materials Science and Engineering, Hunan Institute of Technology, Hengyang 421002, China.
  • He WM; School of Chemistry and Chemical Engineering, University of South China, Hengyang 421001, China.
J Org Chem ; 89(9): 6117-6125, 2024 May 03.
Article em En | MEDLINE | ID: mdl-38654588
ABSTRACT
The first paired electrolysis-enabled arylation of quinoxalin-2(1H)-ones was achieved using cyanoarenes as the arylation reagents. A variety of 3-arylquinoxalin-2(1H)-ones with various important functional groups were obtained in moderate to good yields under metal- and chemical oxidant-free conditions. With a pair of reductive and oxidative processes occurring among the substrates and reaction intermediates, the power consumption can be dramatically reduced.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem 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: J Org Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China