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    Please use this identifier to cite or link to this item: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/76958

    Title: Regioselectivity in the Ring Opening of Epoxides for the Synthesis of Aminocyclitols from D-(-)-Quinic Acid
    Authors: Shih, Tzenge-Lien;Yang, Shu-Yu
    Contributors: 淡江大學化學學系
    Keywords: aminocyclitols;epoxides;glycosidase inhibitors;D-(-)-quinic acid;regioselective ring opening
    Date: 2012-07
    Issue Date: 2012-05-23 10:20:56 (UTC+8)
    Publisher: Basel: M D P I AG
    Abstract: Efficient syntheses of four aminocyclitols are reported. Each synthesis is accomplished in eight steps starting from D-(-)-quinic acid. The key step involves a highly regioselective ring opening of epoxides by sodium azide.
    Relation: Molecules 17(4), pp.4498-4507
    DOI: 10.3390/molecules17044498
    Appears in Collections:[Graduate Institute & Department of Chemistry] Journal Article

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