Studies on the synthesis of 1'-CN-triazolyl- C-ribosides

Org Biomol Chem. 2022 Sep 21;20(36):7261-7269. doi: 10.1039/d2ob01403c.

Abstract

The search for broad-spectrum antiviral compounds is a continuous mandatory effort. The recent approval of the first C-nucleoside carrying a nitrile as a substituent at the C1' position of the ribose ring has raised interest in this underexplored substitution pattern. We have previously reported the development of different 1,2,3-triazolyl-C-ribonucleosides with anticancer and antiviral activities. Herein we report our results on the incorporation of a C1'-CN group in 1,2,3-triazolyl-C-ribonucleosides.

MeSH terms

  • Antiviral Agents / pharmacology
  • Nitriles
  • Nucleosides
  • Ribonucleosides*
  • Ribose*

Substances

  • Antiviral Agents
  • Nitriles
  • Nucleosides
  • Ribonucleosides
  • Ribose