Versatile synthons for optically pure alpha-amino aldehydes and alpha-amino acids: (+)- and (-)-4,5-dialkoxy-2-oxazolidinones

Org Lett. 2001 Mar 22;3(6):897-9. doi: 10.1021/ol015535r.

Abstract

Both enantiomers of trans-5-benzyloxy-4-methoxy- (BMOx) and trans-4,5-dimethoxy-2-oxazolidinones (DMOx), which are readily accessible from simple 2-oxazolone heterocycles, represent good candidates for a new class of chiral synthons for use in the preparation of optically pure alpha-amino aldehydes and alpha-amino acids, respectively.

MeSH terms

  • Aldehydes / chemical synthesis*
  • Aldehydes / chemistry
  • Amines / chemical synthesis*
  • Amines / chemistry
  • Amino Acids / chemical synthesis*
  • Amino Acids / chemistry
  • Indicators and Reagents
  • Molecular Conformation
  • Molecular Structure
  • Oxazolidinones / chemical synthesis*
  • Oxazolidinones / chemistry
  • Stereoisomerism

Substances

  • Aldehydes
  • Amines
  • Amino Acids
  • Indicators and Reagents
  • Oxazolidinones