Green preparation of quinoline derivatives through FeCl3⊙ 6H2O catalyzed Friedlander reaction in ionic liquids

J Wang, X Fan, X Zhang, L Han

Index: Wu, Fang-Wen; Hou, Rei-Sheu; Wang, Huey-Min; Kang, Iou-Jiun; Chen, Ling-Ching Journal of the Chinese Chemical Society, 2012 , vol. 59, # 4 p. 535 - 539

Full Text: HTML

Citation Number: 44

Abstract

The preparation of substituted quinoline derivatives through a Friedlander condensation reaction utilizing the ionic liquid [bmim][BF4] as the reaction medium and iron chloride hexahydrate (FeCl3⊙ 6H2O) as a catalyst is described. The advantages in using this

Related Articles:

Lewis acid-catalyzed cyclization of 3-amino-2-alkenimines. Synthesis of quinolines

[Barluenga, Jose; Cuervo, Humildad; Fustero, Santos; Gotor, Vicente Synthesis, 1987 , # 1 p. 82 - 84]

Lewis acid-catalyzed cyclization of 3-amino-2-alkenimines. Synthesis of quinolines

[Barluenga, Jose; Cuervo, Humildad; Fustero, Santos; Gotor, Vicente Synthesis, 1987 , # 1 p. 82 - 84]

Amberlyst??15??Catalyzed Novel Synthesis of Quinoline Derivatives in Ionic Liquid

[Hou, Rei-Sheu; Wu, Jian-Long; Cheng, Hui-Ting; Xie, You-Teng; Chen, Ling-Ching Journal of the Chinese Chemical Society, 2008 , vol. 55, # 4 p. 915 - 918]

RuCl2 (dmso) 4 Catalyzes the Solvent??Free Indirect Friedländer Synthesis of Polysubstituted Quinolines from Alcohols

[Martinez, Ricardo; Ramon, Diego J.; Yus, Miguel European Journal of Organic Chemistry, 2007 , # 10 p. 1599 - 1605]

More Articles...