Copper-mediated trimethylsilyl azide in amination of bromoflavonoids to synthesize unique aminoflavonoids
TL Shih, CE Chou, WY Liao, CA Hsiao
Index: Shih, Tzenge-Lien; Chou, Chi-En; Liao, Wen-Yu; Hsiao, Chih-Ang Tetrahedron, 2014 , vol. 70, # 23 p. 3657 - 3664
Full Text: HTML
Citation Number: 2
Abstract
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.
Related Articles:
Synthetical experiments in the chromone group
[Anand; Venkataraman Proceedings - Indian Academy of Sciences, Section A, 1947 , # 26 p. 279,282]
Synthetical experiments in the chromone group
[Anand; Venkataraman Proceedings - Indian Academy of Sciences, Section A, 1947 , # 26 p. 279,282]