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    National Tsing Hua University Institutional Repository > 理學院 > 化學系 > 期刊論文 >  Synthesis of biologically potent alpha 1 -> 2-linked disaccharide derivatives via regioselective one-pot protection-glycosylation


    Please use this identifier to cite or link to this item: http://nthur.lib.nthu.edu.tw/dspace/handle/987654321/56534


    Title: Synthesis of biologically potent alpha 1 -> 2-linked disaccharide derivatives via regioselective one-pot protection-glycosylation
    Authors: Wang, CC;Lee, JC;Luo, SY;Fan, HF;Pai, CL;Yang, WC;Lu, LD;Hung, SC
    教師: 洪上程
    Date: 2002
    Publisher: Wiley-Blackwell
    Relation: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, Wiley-Blackwell, Volume 41, Issue 13, 2002, Pages 2360-2362
    Keywords: BENZOYLATION
    TRIETHYLSILANE
    OLIGOSACCHARIDES
    ALKYLATION
    METAL-COMPLEXES
    UNSYMMETRICAL ETHERS
    GLOBO-H
    LIPASE-CATALYZED ACYLATION
    TUMOR-ASSOCIATED ANTIGEN
    CARBONYL-COMPOUNDS
    Abstract: A highly regioselective benzyl and allyl protection of d-hexopyranosides allows their application in the synthesis of biologically potent α1→2 linked disaccharide derivatives by means of a regioselective one-pot protection–glycosylation (see scheme).
    URI: http://as.wiley.com/
    http://nthur.lib.nthu.edu.tw/dspace/handle/987654321/56534
    Appears in Collections:[化學系] 期刊論文

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