Abstract
When N-methylated 4-aryl-5-oxo-4,5-dihydroindeno[1,2-b]pyridines are oxidized with hydrogen peroxide in the presence of perchloric acid, in addition to the formation of the indenopyridinium perchlorates, cleavage of the dihydropyridine ring occurs, giving the 2-arylideneindan-1,3-dione.
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