Abstract
The 5-aroylpyrimidine nucleoside oximes 3-10 were prepared in moderate to good yield by the reaction of the corresponding pyrimidine nucleosides 2a-d with stable nitrile oxides. The nitrile oxides were situ from the corresponding hydroximoyl chlorides 1a-e. From these reactions, only the 1,9-addition products 3-10 were obtained. No products of cycloaddition could be isolated
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