Synthesis of peptidomimetics based on iminosugar and β-D- glucopyranoside scaffolds and inhibiton of HIV-protease

Florence Chery, Linda Cronin, Julie L. O'Brien, Paul V. Murphy

Research output: Contribution to journalArticlepeer-review

Abstract

Synthetic routes to peptidomimetic compounds derived from saccharide scaffolds are described. The regioselective introduction of pivaloyl groups was achieved from N-benzyloxycarbonyl protected 1-deoxymannojirimycin or via D-fructopyranosides. The results from biological evaluation of the saccharide derivatives as HIV-protease inhibitors are included.

Original languageEnglish
Pages (from-to)6597-6608
Number of pages12
JournalTetrahedron
Volume60
Issue number31
DOIs
Publication statusPublished - 26 Jul 2004
Externally publishedYes

Keywords

  • Azasugar
  • Glucopyranoside
  • HIV-protease
  • Iminosugar
  • Peptidomimetic

Fingerprint

Dive into the research topics of 'Synthesis of peptidomimetics based on iminosugar and β-D- glucopyranoside scaffolds and inhibiton of HIV-protease'. Together they form a unique fingerprint.

Cite this