| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218356 | Tetrahedron | 2012 | 6 Pages |
Abstract
The synthesis of new series of oxazolidinones having sulfonamide moieties is described. These compounds are synthesized in good yield starting prochiral 1,3-dichloro-2-propanol and chlorosulfonyl isocyanate. This strategy involves the formation of carboxylsulfamide by carbamoylation–sulfamoylation reaction followed by intermolecular cyclization. In order to determine the enantioselectivity during the cyclization step, X-ray studies of products are performed.
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