淡江大學機構典藏:Item 987654321/97927
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    題名: Copper-mediated trimethylsilyl azide in amination of bromoflavonoids to synthesize unique aminoflavonoids
    作者: Shih, Tzenge-Lien;Chou, Chi-En;Liao, Wen-Yu;Hsiao, Chih-Ang
    貢獻者: 淡江大學化學學系
    關鍵詞: Aminoflavonoids;Baker–Venkataraman rearrangement;Claisen–Schmidt reaction;Copper-mediated amination;Trimethylsilyl azide
    日期: 2014-06-01
    上傳時間: 2014-05-01 14:00:06 (UTC+8)
    出版者: Kidlington: Pergamon
    摘要: 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.
    關聯: Tetrahedron 70, pp.3657-3664
    DOI: 10.1016/j.tet.2014.04.022
    顯示於類別:[化學學系暨研究所] 期刊論文

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