Abstract
The oxidation of methyl-substituted (in the pyridine and benzene rings) benzo[g]isoquinolines to substituted 2-azaanthraquinones was realized. It was established that the pyridine ring is partially reduced to give 1,2,3,4-tetrahydrobenzo[g]isoquinolines in the hydrogenation of benzo[g]isoquinolines in the presence of rhenium heptasulfide.
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