An unusual intramolecular hetero-Diels-Alder cycloaddition

J Org Chem. 2005 Apr 15;70(8):3332-5. doi: 10.1021/jo0500131.

Abstract

A new reaction of erythronolides, an intramolecular hetero-Diels-Alder, has been discovered. Heated aqueous alcoholic solutions of ABT-773 (1) and its cis isomer (3) convert slowly to cycloadducts 2 and 4, respectively. Optimal reaction conditions, mechanistic studies supported by molecular modeling, and biological activity data are reported. Single-crystal X-ray structures for both adducts 2 and 4 have been obtained.

MeSH terms

  • Catalysis
  • Crystallography, X-Ray
  • Cyclization
  • Erythromycin / analogs & derivatives*
  • Erythromycin / chemistry*
  • Ketolides / chemistry*
  • Molecular Conformation
  • Molecular Structure
  • Stereoisomerism

Substances

  • Ketolides
  • Erythromycin
  • cethromycin