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首页> 外文期刊>Synlett >Reductive ring opening of 6-deoxy-6-iodopyranosides and 5-deoxy-5-iodofuranosides by manganese. A convenient procedure for the preparation of chiral 5-hexenals and 4-pentenals
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Reductive ring opening of 6-deoxy-6-iodopyranosides and 5-deoxy-5-iodofuranosides by manganese. A convenient procedure for the preparation of chiral 5-hexenals and 4-pentenals

机译:锰对6-脱氧-6-碘吡喃糖苷和5-脱氧-5-碘呋喃糖苷的还原性开环。制备手性5-己烯醛和4-戊烯醛的简便方法

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摘要

Reaction of fully protected 6-iodopyranosides and 5-iodofuranosides with Mn in the presence of trimethylsilyl chloride and PbCl2 (Takai-conditions) afforded the corresponding 5-hexenals and 4-pentenals in good to moderate yields. [References: 12]
机译:在三甲基甲硅烷基氯和PbCl2存在下,完全保护的6-碘吡喃糖苷和5-碘呋喃糖苷与Mn的反应(Takai条件)可提供相应的5-己烯醛和4-戊烯醛,产率中等至中等。 [参考:12]

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