Methods of synthesizing pharmacologically useful oxazolidinones are disclosed, and, in particular, a method of manufacturing a 5-(tert-butylcarbamoyl)-aminomethyl-oxazolidinone by condensing a carbamate with a tert-butylcarbamoyl protected derivative of glycidylamine or 3-amino-1-halopropanol.

 
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< Substituted sulfonylphenylheterocycles as cyclooxygenase-2 and 5-lipoxygenase inhibitors

< 3,4,5-trisubstituted aryl nitrone compounds and pharmaceutical compositions containing the same

> Lipid peroxide-lowering compositions

> Reagents for intracellular delivery of macromolecules

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