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 |
| Creators | Feuillet, F. J. P., Niyadurupola, D. G., Green, R., Cheeseman, M. and Bull, S. D. |
| DOI | 10.1055/s-2005-865212 |
| Departments | Faculty of Science > Chemistry |
| Refereed | Yes |
| Status | Published |
| ID Code | 4816 |
| Additional Information | ID number: ISI:000228951700003 |
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