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首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of Quinolines via Pd/C-Catalyzed Cyclization of 2-Aminobenzyl Alcohol with Ketones
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Synthesis of Quinolines via Pd/C-Catalyzed Cyclization of 2-Aminobenzyl Alcohol with Ketones

机译:通过Pd / C催化的2-氨基苄醇与酮的环化反应合成喹啉

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摘要

It is known that quinoline plays an important role as a basic skeleton for the design of many pharmacologically active compounds such as antiasthmatic,anti-inflammatory and antimalarial.1 During the course of our studies directed towards C-N bond activation,we have reported the ruthenium-catalyzed synthesis of quinolines via an alkyl or alkanol group transfer from alkylamines or alkanolamines to N-atom of anilines (amine exchange reaction),followed by cascade isomerization and cyclization of 3-(2-aminophenyl)-l-arylprop-2-yn-1-ols.
机译:众所周知,喹啉在设计许多药理活性化合物(例如抗哮喘,抗炎和抗疟疾)中起着基本骨架的重要作用。1在我们针对CN键激活的研究过程中,我们报道了钌通过烷基或链烷醇基团从烷基胺或链烷醇胺转移到苯胺的N原子上的催化合成喹啉(胺交换反应),随后是3-(2-氨基苯基)-1-芳基丙-2-yn-的级联异构化和环化1-ols。

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