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Synthesis and application of N-hydroxy(tetrahydrofuran-2-yl)amines

机译:N-羟基(四氢呋喃-2-基)胺的合成与应用

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摘要

Data on synthesis, reactivity and bioactivity of N-hydroxy(tetrahydrofuran-2-yl)amines were discussed in the present review. General approaches to chiral N-glycosylhydroxylamines based on reactions of hydroxylamine with cyclic five-membered hemiacetals or dihydrofurans as well as reactions of tetrahydrofuran-containing nitrones with nucleophiles were systematized. The application of N-hydroxy(tetrahydrofuran-2-yl)amines in the synthesis of chiral heterocycles, aminophosphonic acids, N-hydroxypropargylamines, as well as natural compounds (for example, sieboldin A), pharmaceuticals (Zileuton) and their analogs was demonstrated. It was found that depending on substituents, N-hydroxy(tetrahydrofuran-2-yl)-amines can act as lipoxygenase inhibitors, and show antioxidant, antitumor, antibacterial, and other types of activities.
机译:本综述讨论了N-羟基(四氢呋喃-2-基)胺的合成,反应性和生物活性的数据。 基于羟胺的反应与环状五元半缩醛或二氢呋喃的反应以及含四氢呋喃的亚硝酸核系物的反应的一般方法得到了系统化。 证实了N-羟基(四氢呋喃-2-基)胺在合成手性杂环,氨基膦酸,N-羟丙基胺和天然化合物(例如,Sieboldin A),药物(Zileuton)及其类似物中的应用 。 发现取决于取代基,N-羟基(四氢呋喃-2-基) - 胺可以作为脂氧基酶抑制剂,并显示抗氧化剂,抗肿瘤,抗菌和其他类型的活性。

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