Abstract
Regio- and stereo-controlled isomerization of 1,2-diaroyl-3-aryl aziridines to the corresponding N-((Z)-1-oxo-1,3-diphenylprop-2-en-2-yl) benzamide in the presence of diethyl thiourea in room temperature is described. A plausible mechanism has been proposed. The structures of the products were confirmed by X-ray analysis.
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