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Abstract
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New and expedient routes have been reported, which allows the regio-, chemo- and stereoselective preparation of 4,5-disubstituted oxazolidin-2-ones 2, based on the reaction of the α-epoxyketones 1 with urea, thiourea or sodium thiocyanate as promising starting materials, in the presence of a catalytic amount of p-toluenesulphunic acid (PTSA) in DMF.
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