1107620-86-9Relevant academic research and scientific papers
Para substituted benzaldehydes as expedient reagents for the oxidative aromatization of hydroquinoline
Majumdar, Poulomi,Pati, Anita,Behera, Rajani K.,Behera, Ajaya Kumar
, p. 703 - 712 (2013/07/05)
A Cannizzaro-type reaction of tetrahydro-5(1H)-quinolinones with para substituted benzaldehydes in the presence of a base formed the corresponding quinoline and aryl methanol rather than arylidene derivatives because of the oxidation of tetrahydroquinoline and reduction of benzaldehydes as a result of unprecedented hydride transfer from tetrahydroquinoline to arylaldehydes. The reaction proceeds best with the participation of substituents with +M effect in substrate molecule.
A facile and expeditious microwave-assisted synthesis of 4-aryl-2-ferrocenyl-quinoline derivatives via multi-component reaction
Tu, Shu-Jiang,Yan, Shu,Cao, Xu-Dong,Wu, Shan-Shan,Zhang, Xiao-Hong,Hao, Wen-Juan,Han, Zheng-Guo,Shi, Feng
experimental part, p. 91 - 96 (2009/03/12)
An efficient and rapid route for the synthesis of 4-aryl-2-ferrocenyl-quinoline derivatives through microwave-assisted multi-component reaction of acetylferrocene with aromatic aldehyde and dimedone in the presence of ammonium acetate using DMF as reactio
