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.
| Original language | English |
|---|---|
| Pages (from-to) | 3657-3664 |
| Number of pages | 8 |
| Journal | Tetrahedron |
| Volume | 70 |
| Issue number | 23 |
| DOIs | |
| State | Published - 10 06 2014 |
| Externally published | Yes |
Keywords
- Aminoflavonoids
- Baker-Venkataraman rearrangement
- Claisen-Schmidt reaction
- Copper-mediated amination
- Trimethylsilyl azide