Alkyne-azide click chemistry mediated carbanucleosides synthesis

Nucleosides Nucleotides Nucleic Acids. 2007;26(10-12):1391-4. doi: 10.1080/15257770701534139.

Abstract

Hitherto unknown 1,4-disubstituted-[1,2,3]-triazolo-4',4'-dihydroxymethyl-3'-deoxy carbanucleosides were synthesized based on a "click approach." Various alkynes were introduced on a key azido intermediate by the "click" 1,3-dipolar Huisgen cycloaddition. Their antiviral activities and cellular toxicities were evaluated on vaccinia virus. None of the synthesized compounds exhibited a significant antiviral activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Antiviral Agents / chemical synthesis*
  • Azides / chemistry*
  • Cyclization
  • Microwaves
  • Molecular Structure
  • Nucleosides / chemical synthesis*
  • Triazoles / chemical synthesis*

Substances

  • Alkynes
  • Antiviral Agents
  • Azides
  • Nucleosides
  • Triazoles