Rearrangements and racemisation during the synthesis of L-serine derived oxazolidin-2-ones

Bew, Sean P., Bull, Steven D., Davies, Stephen G., Savory, Edward D. and Watkin, David J. (2002) Rearrangements and racemisation during the synthesis of L-serine derived oxazolidin-2-ones. Tetrahedron, 58 (46). pp. 9387-9401. ISSN 0040-4020

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Abstract

The propensity for N-Boc-4-hydroxymethyl-oxazolidin-2-ones to undergo rapid O-O and N-O carbonyl transfer makes these L-serine derived chiral auxiliaries unsuitable for attachment to polymers. © 2002 Elsevier Science Ltd. All rights reserved.

Item Type: Article
Faculty \ School: Faculty of Science > School of Chemistry
Faculty of Science > School of Environmental Sciences
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Depositing User: Rachel Smith
Date Deposited: 20 Apr 2011 10:46
Last Modified: 21 Apr 2020 20:42
URI: https://ueaeprints.uea.ac.uk/id/eprint/29666
DOI: 10.1016/S0040-4020(02)01223-1

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