Jump to main content
Jump to site search

Issue 20, 1994
Previous Article Next Article

A new route to oxazolidinones

Abstract

The oxazolidinones 5 and 7 have been prepared by coupling Grignard reagents with N-alkoxycarbonyl-α-amino esters. Hydrolysis of oxazolidinones 5 afforded β-amino alcohols with good yield and enantiomeric excess.

Back to tab navigation

Article type: Paper
DOI: 10.1039/P19940003041
Citation: J. Chem. Soc., Perkin Trans. 1, 1994,0, 3041-3042
  •   Request permissions

    A new route to oxazolidinones

    D. Delaunay and M. L. Corre, J. Chem. Soc., Perkin Trans. 1, 1994, 0, 3041
    DOI: 10.1039/P19940003041

Search articles by author

Spotlight

Advertisements