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

Bew, Sean P. ORCID: https://orcid.org/0000-0002-9087-9463, 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 (former - to 2024) Faculty of Science > School of Environmental Sciences
UEA Research Groups:	Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Materials and Catalysis (former - to 2025) Faculty of Science > Research Groups > Synthetic and Medicinal Chemistry
Related URLs:	https://www.scopus.com/pages/publication...
Depositing User:	Rachel Smith
Date Deposited:	20 Apr 2011 10:46
Last Modified:	18 Jun 2026 15:49
URI:	https://ueaeprints.uea.ac.uk/id/eprint/29666
DOI:	10.1016/S0040-4020(02)01223-1

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