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

Author

Tzenge Lien Shih
Chi En Chou
Wen Yu Liao, Missouri University of Science and TechnologyFollow
Chih Ang Hsiao

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.

Recommended Citation

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

Department(s)

Civil, Architectural and Environmental Engineering

Comments

National Science Council, Grant NSC-102-2113-M-032-003

Keywords and Phrases

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

International Standard Serial Number (ISSN)

1464-5416; 0040-4020

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2023 Elsevier, All rights reserved.

Publication Date

10 Jun 2014