首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of Some Novel Class of Regioselective Spiro Isoxazolidine Derivatives viavia 1,3‐Dipolar Cycloaddition Reaction of N‐N‐ Benzyl‐ C‐C‐ fluoro‐substituted Phenyl Nitrones in Ionic Liquid
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Synthesis of Some Novel Class of Regioselective Spiro Isoxazolidine Derivatives viavia 1,3‐Dipolar Cycloaddition Reaction of N‐N‐ Benzyl‐ C‐C‐ fluoro‐substituted Phenyl Nitrones in Ionic Liquid

机译:综合一些新颖的地区血红素胰岛唑胺衍生物通过 n - n- enbzyl- c - 离子液体中的C-氟取代苯基亚硝酮

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摘要

> Synthesis of some new class of regioselective spiro isoxazolidine derivatives have been described using N‐ benzyl‐ C‐ fluoro substituted‐phenyl nitrones with new dipolarophiles via 1,3‐dipolar cycloaddition reaction in ionic liquid. The novel spiro cycloadducts found to exhibit good synthetic potentiality as they could be converted into synthetically more important spiro 1,3‐amino alcohols. Simple reaction methodology, noninvolvent of catalysts, good to excellent yields, and greener approaches are the important features noticed in this syntheses.
机译: >一些新的血液选择性螺索恶唑烷衍生物已经使用< Fi> N - 苄基 - C - 氟代取代 - 苯基亚硝钠,具有新的二极管通过离子液体的1,3-偶极环加油反应。 发现新颖的螺旋环形化学,发现良好的合成潜力,因为它们可以转化为综合更重要的螺氧1,3-氨基醇。 简单的反应方法,催化剂的非植物,良好的优质产率,更环保的方法是该合成中注意到的重要特征。

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