21923-43-3Relevant articles and documents
Synthesis and trypanocidal activity of substituted 2,4-diarylquinoline derivatives
Oluwafemi, Kola A.,Phunguphungu, Siyolise,Gqunu, Sinalo,Isaacs, Michelle,Hoppe, Heinrich C.,Klein, Rosalyn,Kaye, Perry T.
, (2021/06/17)
A small library of nine, novel 2,4-diarylquinoline derivatives has been prepared in high yield via convenient one-or two-step routes from a series of substituted 2-Aminobenzophenones. None of the products exhibited toxicity at 20 uM against human cervix a
Dowex-50w promoted friedlaender synthesis of substituted quinolines under solvent-free conditions
Wang, Huey-Min,Hou, Rei-Sheu,Du, Hau-Dung,Kang, Iou-Jiun,Chen, Ling-Ching
experimental part, p. 331 - 338 (2011/04/15)
An efficient method for the synthesis of substituted quinolines using Dowex-50W ion exchange resin as reusable eco-friendly catalyst vai Friedlaender annulation under solvent-free conditions is described. The Japan Institute of Heterocyclic Chemistry.
Preparation of 2-arninpbenzophenones and polysubstituted quinolines through Sml2 promoted reductive cleavage of 3-aryl-2,1-benzisoxazoles
Fan, Xuesen,Zhang, Xinying,Zhang, Yongmin
, p. 637 - 643 (2007/10/03)
Promoted by SmI2, 3-aryl-2,1-benzisoxazoles underwent reductive cleavage of the N - O bond leading to 2-aminobenzophenones in high yields upon protonation. Otherwise, if ketones with active methylene group were added to the reaction mixture prior to protonation, the desired poly substituted quinolines could be obtained under mild conditions in a one-pot manner.
