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Direct C3 Alkoxylation of Quinoxalin-2(1H)-ones with Alcohols via Cross-Dehydrogenative Coupling under Catalyst-Free Conditions.
Yang, Qiming; Han, Xulin; Zhao, Jiquan; Zhang, Hong-Yu; Zhang, Yuecheng.
Afiliación
  • Yang Q; School of Chemical Engineering and Technology, Hebei Provincial Key Lab of Green Chemical Technology & High Efficient Energy Saving , Hebei University of Technology , Tianjin 300130 , P. R. China.
  • Han X; School of Chemical Engineering and Technology, Hebei Provincial Key Lab of Green Chemical Technology & High Efficient Energy Saving , Hebei University of Technology , Tianjin 300130 , P. R. China.
  • Zhao J; School of Chemical Engineering and Technology, Hebei Provincial Key Lab of Green Chemical Technology & High Efficient Energy Saving , Hebei University of Technology , Tianjin 300130 , P. R. China.
  • Zhang HY; School of Chemical Engineering and Technology, Hebei Provincial Key Lab of Green Chemical Technology & High Efficient Energy Saving , Hebei University of Technology , Tianjin 300130 , P. R. China.
  • Zhang Y; School of Chemical Engineering and Technology, Hebei Provincial Key Lab of Green Chemical Technology & High Efficient Energy Saving , Hebei University of Technology , Tianjin 300130 , P. R. China.
J Org Chem ; 84(18): 11417-11424, 2019 09 20.
Article en En | MEDLINE | ID: mdl-31418562
ABSTRACT
A facile and effective alkoxylation protocol of quinoxalin-2(1H)-ones with primary or secondary alcohols via cross-dehydrogenative coupling under catalyst-free conditions has been disclosed. This method provides a powerful and convenient access to 3-alkoxylquinoxalin-2(1H)-ones in good to excellent yields by utilizing PhI(OTFA)2 as an oxidant and allows to easily obtain potential drug molecules containing 3-alkoxylquinoxalin-2(1H)-one skeletons.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2019 Tipo del documento: Article
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