作者:Prattya Nealmongkol、Jordan Calmes、Somsak Ruchirawat、Nopporn Thasana
DOI:10.1016/j.tet.2016.12.051
日期:2017.2
The chemoselective synthesis of phenanthridinones was studied using copper(I)- and palladium(II)-catalyzed CN bond formation with various bases, ligands, and solvents. Phenanthridinones were obtained from 2-halobiarylcarboxylates and amines in a one-pot reaction. The phenanthridinones and heterocyclic-fused lactam derivatives were accomplished using developed methods.
利用铜(I)和钯(II)催化的C N键与各种碱,配体和溶剂的形成,研究了菲啶酮的化学选择性合成。从一锅反应中由2-卤代二芳基羧酸盐和胺获得菲啶酮。菲啶酮和杂环稠合的内酰胺衍生物是使用发达的方法完成的。