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Facile and stereo-controlled synthesis of 2-deoxynojirimycin, Miglustat and Miglitol

机译:2-脱氧野oji霉素,米格司他和米格列醇的简便且立体控制的合成

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摘要

A novel and facile synthesis of a series of the biologically significant iminosugar derivatives including 2-deoxynojirimycin, Miglustat and Miglitol is reported. The synthesis features a strategic double inversion mechanism for securing the desired stereochemistry at C5 position of such glucose-type carbohydrate mimetics, representing a practical and remarkable improvement on the previously reported method that suffers from the loss of the stereo-control during the reaction process.
机译:报道了一种新颖且容易的合成一系列具有生物学意义的亚氨基糖衍生物的方法,包括2-脱氧野series霉素,米格司他和米格列醇。该合成具有策略性的双重转化机制,用于确保此类葡萄糖型碳水化合物模拟物在C5位置处具有所需的立体化学,代表了对先前报道的方法的实用且显着的改进,该方法在反应过程中失去了立体控制。

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