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. © 2014 Elsevier Ltd. All rights reserved.
| Original language | American English |
|---|---|
| Journal | Tetrahedron |
| Volume | 70 |
| DOIs | |
| State | Published - Jun 10 2014 |
Keywords
- Aminoflavonoids
- Baker-Venkataraman rearrangement
- Claisen-Schmidt reaction
- Copper-mediated amination
- Trimethylsilyl azide
Disciplines
- Architectural Engineering
- Civil and Environmental Engineering
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