首页> 外文期刊>Carbohydrate research >Regioselective synthesis of alditol vicinal bis-cyclic thionocarbonates via alditol stannylene acetal complexes as a short and efficient route #alpha#,#omega#-diiodoalditol derivatives
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Regioselective synthesis of alditol vicinal bis-cyclic thionocarbonates via alditol stannylene acetal complexes as a short and efficient route #alpha#,#omega#-diiodoalditol derivatives

机译:通过醛糖醇亚锡缩醛配合物的区域选择性合成醛糖醇双环硫代碳酸酯作为一种短而有效的途径#α#,#omega#-二碘代糖醇衍生物

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摘要

The bis-cyclic thionocarbonates of alditols (pentitols and hexitols) were quickly and easily obtained from alditol stannylene complexes and phenyl chlorothionoformate (PhOC(S)Cl) in good yields. Acetylation of isolated free alditol bis-thionocarbonates and subsequent iodination using methyl iodide under pressure led to #alpha#,#omega#-diiodo derivatives of alditols in good to excellemnt isolated yields. (67-93%).
机译:醛糖醇(戊糖醇和己糖醇)的双环硫代碳酸盐可以快速,轻松地从醛糖醇亚锡配合物和苯基氯硫代甲酸酯(PhOC(S)Cl)中以高收率获得。分离的游离醛糖醇双硫代碳酸酯的乙酰化和随后在压力下使用甲基碘的碘化作用导致醛醇的α-,ω-二碘代衍生物具有良好的分离产率。 (67-93%)。

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