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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Facile preparative HPLC enantioseparation of racemic drugs using chiral stationary phases based on mono-6~A-azido-6~A-deoxy-perphenylcarbamoylated #beta#-cyclodextrin immobilized on silica gel
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Facile preparative HPLC enantioseparation of racemic drugs using chiral stationary phases based on mono-6~A-azido-6~A-deoxy-perphenylcarbamoylated #beta#-cyclodextrin immobilized on silica gel

机译:基于固定在硅胶上的单-6〜A-叠氮基-6〜A-脱氧-全苯基氨基甲酰化的#beta#-环糊精的手性固定相,用于消旋药物的简便制备型HPLC对映体分离

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摘要

Immobilized chiral stationary phases (CSP)s from mono-6~A-azido-6~A-deoxy-perphenylcarbamoylated #beta#-cyclodextrin were prepared using an extended application of the Staudinger reaction. Their application in preparative enantioseparations of racemic mixtures was demonstrated using atropine, bendroflumethiazide and four #beta#-adrenergic blocking agents under reversed phase conditions.
机译:使用施陶丁格反应的扩展应用,制备了由单-6-A-叠氮基-6-A-脱氧-全苯基氨基甲酰基化的β-β-环糊精固定的手性固定相(CSP)。在逆流条件下,使用阿托品,苯氟甲酰肼和四种#β#-肾上腺能阻滞剂证明了它们在外消旋混合物制备对映体分离中的应用。

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