53855-23-5Relevant academic research and scientific papers
A highly selective method for the synthesis of 1,3-diarylbenzo[f]quinoline derivatives catalyzed by silver triflate
Wang, Xiang-Shan,Zhou, Jie,Zhang, Mei-Mei,Wang, Wei,Li, Yu-Ling
experimental part, p. 935 - 938 (2012/07/16)
The three-component reactions of aromatic aldehydes, naphthalen-2-amine, and phenylacetylene catalyzed by AgOTf in toluene selectively gave 1,3-diarylbenzo[f]quinolines in high yields. This procedure provides an efficient method for the synthesis of benzo[f]quinolines under mild reaction conditions and with high yields, high selectivity, and operational simplicity. Springer-Verlag 2011.
An efficient synthesis of 1,3-diarylbenzo[f]quinolines from 2-halogenated acetophenone, aromatic aldehyde, and naphthalen-2-amine catalyzed by iodine
Wang, Xiang-Shan,Li, Qing,Zhou, Jie,Tu, Shu-Jiang
experimental part, p. 1222 - 1228 (2010/03/04)
(Chemical Equation Presented) The three-component reaction of aromatic aldehyde, naphthalen-2-amine and 2-halogenated acetophenone in THF catalyzed by 5 mol % iodine at reflux unexpectedly gave 1,3-diarylbenzo[f]quinolines, with halogen losing in the form
An efficient and highly selective method for the synthesis of 3-arylbenzo-quinoline derivatives catalyzed by iodine via three-component reactions
Wang, Xiang-Shan,Li, Qing,Wu, Jian-Rong,Li, Yu-Ling,Yao, Chang-Sheng,Tu, Shu-Jiang
experimental part, p. 1902 - 1910 (2009/04/04)
A mild, efficient and highly selective method for the synthesis of benzo[f]quinoline derivatives via three-component reactions of arylaldehydes, naphthalen-2-amine and ketones or β-keto esters using iodine as catalyst is described. It should be noted that only one product was obtained, with high selectivity, when ketones or β-keto esters with two different α-hydrogen atoms were chosen as reactants.
