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

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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

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

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