Copper-mediated trimethylsilyl azide in amination of bromoflavonoids to synthesize unique aminoflavonoids

  • Tzenge Lien Shih*
  • , Chi En Chou
  • , Wen Yu Liao
  • , Chih Ang Hsiao
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

11 Scopus citations

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 languageEnglish
Pages (from-to)3657-3664
Number of pages8
JournalTetrahedron
Volume70
Issue number23
DOIs
StatePublished - 10 06 2014
Externally publishedYes

Keywords

  • Aminoflavonoids
  • Baker-Venkataraman rearrangement
  • Claisen-Schmidt reaction
  • Copper-mediated amination
  • Trimethylsilyl azide

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