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首页> 外文期刊>Chemistry of heterocyclic compounds >Recyclization of 1,4-dihydropyridine derivatives in acidic medium
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Recyclization of 1,4-dihydropyridine derivatives in acidic medium

机译:1,4-二氢吡啶衍生物在酸性介质中的再循环

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摘要

The recyclization of 1,4-dihydropyridines in aqueous-alcoholic hydrochloric acid medium proceeds with cleavage of a C-N bond and pyridine ring opening. Cyclohexenone derivatives are formed as a result of the subsequent intramolecular crotonic condensation of the acyclic intermediate. The leaving carbonyl substituents depart simultaneously with recyclization, depending on the acidity of the reaction medium.
机译:1,4-二氢吡啶在含水酒精盐酸介质中的环化反应是通过C-N键的裂解和吡啶的开环进行的。由于无环中间体随后的分子内巴豆酸缩合,形成了环己烯酮衍生物。取决于反应介质的酸度,剩余的羰基取代基在再循环的同时分离。

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