A convergent ring-closing metathesis approach to carbohydrate-based macrolides with potential antibiotic activity

J Org Chem. 2005 Nov 25;70(24):10109-12. doi: 10.1021/jo051021k.

Abstract

[reaction: see text] An efficient convergent approach has been developed for the construction of novel, non-natural, carbohydrate-based macrolides. The key step in the synthesis is the formation of the macrocyclic ring via a ring-closing metathesis reaction. The obtained macrolide analogues have been screened for biological activity against gram-positive and gram-negative bacteria, including resistant strains, yeasts, and molds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis*
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Carbohydrates / chemistry*
  • Cyclization
  • Macrolides / chemical synthesis*
  • Macrolides / chemistry
  • Macrolides / pharmacology*
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Stereoisomerism

Substances

  • Anti-Bacterial Agents
  • Carbohydrates
  • Macrolides