Stereoselective rearrangement of beta-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones

F J P Feuillet, D G Niyadurupola, R Green, M Cheeseman, S D Bull

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Zinc alkoxides of syn- or anti-β-hydroxy-N-acyloxazolidin-2-ones undergo stereoselective rearrangement to afford their corresponding syn- or anti-N-2-hydroxyethyl-1,3-oxaziliane-2,4-diones in good yield.
Original languageEnglish
Pages (from-to)1090-1094
Number of pages5
JournalSynlett
Issue number7
DOIs
Publication statusPublished - 2005

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