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首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of Quinoline N-Oxides from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes:Conjugate Addition of Nitroso Intermediate
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Synthesis of Quinoline N-Oxides from the Baylis-Hillman Adducts of 2-Nitrobenzaldehydes:Conjugate Addition of Nitroso Intermediate

机译:由2-硝基苯甲醛的Baylis-Hillman加合物合成喹啉N-氧化物:硝基中间体的共轭加成

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摘要

The Baylis-Hillman reaction is a useful carbon-carbon bond-forming method from activated vinyls and carbonyl compounds.Chemical transformation of the Baylis-Hillman adducts or their derivatives into useful heterocyclic compounds has been studied recently by us and other groups.Especially,conversion of the Baylis-Hillman adducts derived from 2-nitrobenzaldehydes into quinoline skeleton is a useful entry for the quinoline chemistry.
机译:Baylis-Hillman反应是一种有用的由活化的乙烯基和羰基化合物形成碳-碳键的方法。最近,我们和其他研究人员研究了Baylis-Hillman加合物或其衍生物向有用的杂环化合物的化学转化。特别是,转化由2-硝基苯甲醛衍生的Baylis-Hillman加合物形成喹啉骨架是喹啉化学的有用入口。

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