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    Please use this identifier to cite or link to this item: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/97927

    Title: Copper-mediated trimethylsilyl azide in amination of bromoflavonoids to synthesize unique aminoflavonoids
    Authors: Shih, Tzenge-Lien;Chou, Chi-En;Liao, Wen-Yu;Hsiao, Chih-Ang
    Contributors: 淡江大學化學學系
    Keywords: Aminoflavonoids;Baker–Venkataraman rearrangement;Claisen–Schmidt reaction;Copper-mediated amination;Trimethylsilyl azide
    Date: 2014-06-01
    Issue Date: 2014-05-01 14:00:06 (UTC+8)
    Publisher: Kidlington: Pergamon
    Abstract: Aminoflavonoids are unique antioxidants comparing to other abundant flavonoids in nature. Their syntheses and biological activities were scarcely reported. An effectively copper-mediated amination of the corresponding bromoflavonoids to synthesize a series of new aminoflavonoids is described.
    Relation: Tetrahedron 70, pp.3657-3664
    DOI: 10.1016/j.tet.2014.04.022
    Appears in Collections:[Graduate Institute & Department of Chemistry] Journal Article

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