One-pot direct conversion of 2,3-epoxy alcohols into enantiomerically pure 4-hydroxy-4,5-dihydroisoxazole 2-oxides

Org Lett. 2001 Mar 8;3(5):727-9. doi: 10.1021/ol0070379.

Abstract

[structure: see text]. A new methodology for the one-pot direct conversion of 2,3-epoxy alcohols into enantiomerically pure 4-hydroxy-4,5-dihydroisoxazole 2-oxides 1 has been found. The reaction works at room temperature and can be run at the 5-10 g scale. The mixture of 4,5-cis and 4,5-trans isomers obtained can be separated as such or as the bis-TDS ethers. A preliminary example of reductive cleavage of 1 to the corresponding amino polyol is also reported.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemical synthesis*
  • Aluminum Compounds
  • Epoxy Compounds / chemistry*
  • Indicators and Reagents
  • Isoxazoles / chemical synthesis*
  • Lithium Compounds
  • Molecular Conformation
  • Stereoisomerism

Substances

  • Alcohols
  • Aluminum Compounds
  • Epoxy Compounds
  • Indicators and Reagents
  • Isoxazoles
  • Lithium Compounds
  • lithium aluminum hydride