Issue 20, 1994

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.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 3041-3042

A new route to oxazolidinones

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements