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5-磷酰基-3-芳基异噁唑啉的合成及结构表征
引用本文:张长水,叶勇.5-磷酰基-3-芳基异噁唑啉的合成及结构表征[J].有机化学,2012,32(7):1336-1339.
作者姓名:张长水  叶勇
作者单位:1. 河南科技大学化工与制药学院 洛阳471003
2. 郑州大学化学系 河南省磷化工工程技术研究中心 郑州450052
摘    要:通过乙烯基膦酸酯与氧化腈的环加成反应,合成了一系列区域专一的异噁唑啉.化合物3c的单晶X衍射证实产物为5-磷酰基异噁唑啉.目标化合物结构经核磁、电喷雾质谱和元素分析表证,生物活性测试表明这些化合物具有一定的神经氨酸酶抑制活性.

关 键 词:乙烯基膦酸酯  氧化腈  环加成反应  异噁唑啉

Synthesis and Characterization of 5-Phosphonyl-3-arylisoxazoline
Zhang,Changshui , Ye,Yong.Synthesis and Characterization of 5-Phosphonyl-3-arylisoxazoline[J].Chinese Journal of Organic Chemistry,2012,32(7):1336-1339.
Authors:Zhang  Changshui  Ye  Yong
Institution:Zhang,Changshuia Ye,Yong,b(aChemical Engineering & Pharmaceutics College,Henan University of Science & Technology,Luoyang 471003)(bPhosphorus Chemical Engineering Research Center of Henan Province,Department of Chemistry,Zhengzhou University,Zhengzhou 450052)
Abstract:A series of regioselectively isoxazolines were synthesized through cycloaddition reaction of nitrile oxides with vinylphosphonate.The structure of title compound was proved as 5-phosphonyl isoxazoline by X-ray crystallography of compound 3c.Their structures were confirmed by NMR,ESI-MS and elemental analysis.The suppression of the neuraminidase inhibitors was also tested.The result showed that they could inhibit neuraminidase.
Keywords:vinylphosphonates  nitrile oxide  1  3-dipolar cycloaddition  isoxazoline
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