A new route to oxazolidinones
- 1 January 1994
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 20,p. 3041-3042
- https://doi.org/10.1039/p19940003041
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.Keywords
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