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


Reference:

Feuillet, F. J. P., Niyadurupola, D. G., Green, R., Cheeseman, M. and Bull, S. D., 2005. Stereoselective rearrangement of beta-hydroxy-N-acyloxazolidin-2-ones to afford N-2-hydroxyethyl-1,3-oxazinane-2,4-diones. Synlett

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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.

Details

Item Type Articles
CreatorsFeuillet, F. J. P., Niyadurupola, D. G., Green, R., Cheeseman, M. and Bull, S. D.
DOI10.1055/s-2005-865212
DepartmentsFaculty of Science > Chemistry
RefereedYes
StatusPublished
ID Code4816
Additional InformationID number: ISI:000228951700003

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