Copper-mediated Trimethylsilyl Azide In Amination Of Bromoflavonoids To Synthesize Unique Aminoflavonoids
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. © 2014 Elsevier Ltd. All rights reserved.
T. L. Shih et al., "Copper-mediated Trimethylsilyl Azide In Amination Of Bromoflavonoids To Synthesize Unique Aminoflavonoids," Tetrahedron, vol. 70, no. 23, pp. 3657 - 3664, Elsevier, Jun 2014.
The definitive version is available at https://doi.org/10.1016/j.tet.2014.04.022
Civil, Architectural and Environmental Engineering
Keywords and Phrases
Aminoflavonoids; Baker-Venkataraman rearrangement; Claisen-Schmidt reaction; Copper-mediated amination; Trimethylsilyl azide
International Standard Serial Number (ISSN)
Article - Journal
© 2023 Elsevier, All rights reserved.
10 Jun 2014