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首页> 外文期刊>Organic letters >Convenient, in Situ Generation of Anhydrous Hydrogen Iodide for the Preparation of α-Glycosyl Iodides and Vicinal Iodohydrins and for the Catalysis of Ferrier Glycosylation
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Convenient, in Situ Generation of Anhydrous Hydrogen Iodide for the Preparation of α-Glycosyl Iodides and Vicinal Iodohydrins and for the Catalysis of Ferrier Glycosylation

机译:方便,就地生成无水碘化氢,用于制备α-糖基碘化物和邻位碘代醇,并催化氨基糖基化

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摘要

Anhydrous hydrogen iodide is generated in situ by the reaction of solid iodine and a thiol. The HI thus generated has been employed for the efficient preparation of α-glycosyl iodides and vicinal iodohydrins from the corresponding glycosyl acetates and epoxides, respectively, and for Ferrier glycosylation of alcohols and thiols.
机译:无水碘化氢是通过固体碘与硫醇的反应原位生成的。由此产生的HI已被用于分别从相应的乙酸糖基酯和环氧化物有效地制备α-糖基碘化物和邻位碘代醇,以及用于醇和硫醇的ferrier糖基化。

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