首页> 外文期刊>The Journal of Organic Chemistry >Transition metal-mediated stereocontrolled cyclization of urethanes leading to versatile fused piperidines and its application to the synthesis of (+)-prosopinine and (+)-palustrine
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Transition metal-mediated stereocontrolled cyclization of urethanes leading to versatile fused piperidines and its application to the synthesis of (+)-prosopinine and (+)-palustrine

机译:过渡金属介导的氨基甲酸酯的立体控制环化反应,导致多功能的稠合哌啶及其在(+)-脯氨酸和(+)-palustrine合成中的应用

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摘要

Streoselective amino cycloaddition of alkenylamines is one of the most important approaches for the stereo- selective construction of nitrogen heteroalicycles, which form the skeletons of several biologically active natural products and related compounds. Palladium(0)-catalyzed allyic substitution in particular provides efficient ste- reoselective C-N bond formation.
机译:烯基胺的立体选择性氨基环加成是氮杂脂环族立体选择性构建的最重要方法之一,氮杂脂环形成几种具有生物活性的天然产物和相关化合物的骨架。钯(0)催化的烯丙基取代尤其可提供有效的立体选择性C-N键形成。

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