Abstract
Mixtures of stereoisomers of oxiranylhydroxytetrahydropyrimidines were obtained by cyclocondensation of Β-arylacrylyloxiranes with acetamidines or benzamidines; the 2-aryl derivatives of the products give the corresponding dihydropyrimidines and pyrimidines under base-catalysis conditions. In acetic acid dehydration and oxidation are accompanied by opening of the epoxide ring.
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