20668-43-3Relevant academic research and scientific papers
Pd-Catalyzed Alkylation of (Iso)quinolines and Arenes: 2-Acylpyridine Compounds as Alkylation Reagents
Wu, Qingsong,Han, Shuaijun,Ren, Xiaoxiao,Lu, Hongtao,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng
supporting information, p. 6345 - 6348 (2018/10/20)
The first Pd-catalyzed alkylation of (iso)quinolines and arenes is reported. The readily available and bench-stable 2-acylpyridine compounds were used as an alkylation reagent to form the structurally versatile alkylated (iso)quinolines and arenes. The method affords a convenient pathway for the introduction of alkyl groups into organic molecules.
Fast and convenient base-mediated synthesis of 3-substituted quinolines
Mierde, Hans Vander,Voort, Pascal Van Der,Verpoort, Francis
scheme or table, p. 201 - 203 (2009/04/19)
In a convenient method, 3-substituted quinolines are readily synthesized in a two-step process with initial oxazine formation and subsequent base-mediated cyclization.
A copper(II)-catalyzed protocol for modified Friedl?nder quinoline synthesis
Cho, Chan Sik,Ren, Wen Xiu,Shim, Sang Chul
, p. 6781 - 6785 (2007/10/03)
2-Aminobenzyl alcohol reacts with an array of ketones in dioxane at 100 °C in the presence of a catalytic amount of CuCl2 along with KOH under O2 atmosphere to afford the corresponding quinolines in good yields. 2-Aminobenzyl alcohol is also oxidatively coupled and cyclized with various aldehydes by step-by-step procedure, an initial treatment of 2-aminobenzyl alcohol in the presence of CuCl2 and KOH in dioxane under O2 atmosphere and subsequent addition of aldehyde to the mixture followed by stirring under argon atmosphere, to give 3-substituted quinolines in moderate to good yields.
