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Copper-mediated Trimethylsilyl Azide In Amination Of Bromoflavonoids To Synthesize Unique Aminoflavonoids

  • Tzenge Lien Shih
  • , Chi En Chou
  • , Wen Yu Liao
  • , Chih Ang Hsiao

Research output: Contribution to journalArticlepeer-review

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 languageAmerican English
JournalTetrahedron
Volume70
DOIs
StatePublished - 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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