首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Efficient Synthesis of Quinolo-oxepanes Through [3+2] Cycloaddition Reaction of α,β-Unsaturated Ester with Unstabilized Azomethine Ylides
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Efficient Synthesis of Quinolo-oxepanes Through [3+2] Cycloaddition Reaction of α,β-Unsaturated Ester with Unstabilized Azomethine Ylides

机译:通过α,β-不饱和酯与不稳定的甲亚胺叶立德的[3 + 2]环加成反应有效合成喹诺酮-氧杂环戊烷

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摘要

New functionalized quinolo-oxepane were achieved by intramolecular 1,3-dipolar cycloaddition reaction of α,β-unsaturated ester with unstabilized azomethine ylides derived from various a-amino acids with high stereo selectivity and good yields. These derivatives were synthesized via Wittig reaction under mild, neutral conditions in a short duration and consistently good yields. The structures of final compounds were characterized by spectral analysis.
机译:通过α,β-不饱和酯的分子内1,3-偶极环加成反应与衍生自各种α-氨基酸的不稳定的甲亚胺基亚胺的分子内1,3-偶极环加成反应,可以实现高立体选择性和高收率。这些衍生物是通过Wittig反应在温和,中性条件下以较短的持续时间和始终如一的良好收率合成的。最终化合物的结构通过光谱分析表征。

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