Abstract
Abstract The reaction of iminodimagnesium reagent derived from 2-amino-4-methylpyridine with nitrobenzenes was examined. The relative yields of the azoxypyridine formed via condensation and the azopyridines via deoxygenation and oxidative dimerization were explained in terms of weak electron-donating ability of the reagent and the strong electron-accepting ability of the azoxypyridine.
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