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Synthesis of Natural and Sugar-Modified Nucleosides Using the Iodine/Triethylsilane System as N-Glycosidation Promoter

  • Martina Cimafonte
  • , Anna Esposito
  • , Maria De Fenza
  • , Francesco Zaccaria
  • , Daniele D’Alonzo
  • , Annalisa Guaragna
  • University of Naples Federico II

Research output: Contribution to journalScientific articlepeer-review

Abstract

The reagent system based on the combined use of Et3SiH/I2 acts as an efficient N-glycosidation promoter for the synthesis of natural and sugar-modified nucleosides. An analysis of reaction stereoselectivity in the absence of C2-positioned stereodirecting groups revealed high selectivity with six-membered substrates, depending on the nucleophilic character of the nucleobase or based on anomerization reactions. The synthetic utility of the Et3SiH/I2-mediated N-glycosidation reaction was highlighted by its use in the synthesis of the investigational drug apricitabine.

Original languageEnglish
Article number9030
JournalInternational Journal of Molecular Sciences
Volume25
Issue number16
DOIs
Publication statusPublished - Aug 2024
Externally publishedYes

Keywords

  • anomerization
  • apricitabine
  • glycosyl iodide
  • iodine/triethylsilane
  • N-glycosidation
  • nucleosides
  • stereoselectivity

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