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首页> 外文期刊>Angewandte Chemie >Chemoselective Activation of Diethyl Phosphonates: Modular Synthesis of Biologically Relevant Phosphonylated Scaffolds
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Chemoselective Activation of Diethyl Phosphonates: Modular Synthesis of Biologically Relevant Phosphonylated Scaffolds

机译:膦酸二乙基膦酸酯的化学选择性活化:模块化合成生物相关的膦酰化支架

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摘要

Phosphonates have garnered considerable attention for years owing to both their singular biological properties and their synthetic potential. State-of-the-art methods for the preparation of mixed phosphonates, phosphonamidates, phosphonothioates, and phosphinates rely on harsh and poorly selective reaction conditions. We report herein a mild method for the modular preparation of phosphonylated derivatives, several of which exhibit interesting biological activities, that is based on chemoselective activation with triflic anhydride. This procedure enables flexible and even iterative substitution with a broad range of O, S, N, and C nucleophiles.
机译:由于它们的奇异生物学性质及其合成潜力,膦酸盐多年来已经得到了相当大的关注。 用于制备混合膦酸盐,膦酰胺,膦酰基化合物和磷酸盐的最先进的方法依赖于苛刻且选择性的反应条件差。 我们在本文中报告了一种温和的方法,用于模块化膦化衍生物的模块化制备,其中几种表现出有趣的生物活性,这是基于与三氟乙烯酸酐的化学选择性活化。 该程序可以灵活甚至迭代替代,具有宽范围的O,S,N和C亲核官。

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