1,3-dipolar cycloaddition of furfuryl nitrones with acrylates. A convenient approach to protected 4-hydroxypyroglutamic acids

J Org Chem. 2000 Mar 10;65(5):1590-6. doi: 10.1021/jo991560n.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylates / chemistry
  • Acrylates / metabolism*
  • Alkenes / metabolism
  • Cyclization
  • Furaldehyde / analogs & derivatives
  • Furaldehyde / chemistry
  • Furaldehyde / metabolism*
  • Hydroxyproline / analogs & derivatives*
  • Hydroxyproline / chemical synthesis
  • Hydroxyproline / chemistry
  • Hydroxyproline / metabolism
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Molecular Conformation
  • Nitrogen Oxides / chemistry
  • Nitrogen Oxides / metabolism*
  • Pyrrolidonecarboxylic Acid / analogs & derivatives*
  • Pyrrolidonecarboxylic Acid / chemical synthesis*
  • Pyrrolidonecarboxylic Acid / chemistry
  • Pyrrolidonecarboxylic Acid / metabolism
  • Stereoisomerism
  • Thermodynamics

Substances

  • 4-hydroxypyroglutamic acid
  • Acrylates
  • Alkenes
  • Nitrogen Oxides
  • nitrones
  • Furaldehyde
  • Hydroxyproline
  • Pyrrolidonecarboxylic Acid