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首页> 外文期刊>Organic & biomolecular chemistry >Cross 1,3-dipolar cycloadditions of C,N-cyclic azomethine imines with an N-benzyl azomethine ylide: facile access to fused tricyclic 1,2,4-hexahydrotriazines
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Cross 1,3-dipolar cycloadditions of C,N-cyclic azomethine imines with an N-benzyl azomethine ylide: facile access to fused tricyclic 1,2,4-hexahydrotriazines

机译:C,N-环甲亚胺亚胺与N-苄基甲亚胺叶立德的交叉1,3-偶极环加成反应:易于获得稠合的三环1,2,4-六氢三嗪

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摘要

A cross 1,3-dipolar cycloaddition of two different ylides between C,N-cyclic azomethine imines with an in situ-generated nonstabilized azomethine ylide from an N-benzyl precursor was realized. The reactions afforded a clean and facile access to diverse fused tricyclic 1,2,4-hexahydrotriazines in high yields (up to 96%). The chemical structures of the typical compounds were confirmed by X-ray single-crystal structure analysis.
机译:实现了C,N-环偶氮甲亚胺亚胺与N-苄基前体原位生成的非稳定的偶氮甲亚胺叶立德之间两个不同烷基的交叉1,3-偶极环加成。该反应提供了高产率(高达96%)的清洁且容易地获得各种稠合的三环1,2,4-六氢三嗪的方法。通过X射线单晶结构分析确认了典型化合物的化学结构。

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  • 来源
    《Organic & biomolecular chemistry》 |2019年第2期|244-247|共4页
  • 作者单位

    Xinxiang Univ, Coll Chem & Chem Engn, Xinxiang 453000, Peoples R China;

    Xinxiang Univ, Med Coll, Xinxiang 453000, Peoples R China;

    Xinxiang Univ, Coll Chem & Chem Engn, Xinxiang 453000, Peoples R China;

    Xinxiang Univ, Coll Chem & Chem Engn, Xinxiang 453000, Peoples R China;

    Xinxiang Univ, Coll Chem & Chem Engn, Xinxiang 453000, Peoples R China;

    Xinxiang Univ, Coll Chem & Chem Engn, Xinxiang 453000, Peoples R China|Zhejiang Univ, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310058, Zhejiang, Peoples R China;

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