Abstract: | The chemical reduction of 5H-[1]benzopyranno[4,3-d]pyrimidines with lithium aluminum hydrrde leads to 3,4-dihydro derivations. The electro-chemical reducation in acidic medium shows two monoelectronic cathodic waves. In netural or basic medium, substituted compounds in 2 position show a single bielectronic wave while two bielectronic waves are observed for unsubstituted compounds In all cases, preparative electrolysis lead to a hydrodimer in the 4,4′-positiom. |