Abstract
Previously unknown 2-methoxy(or ethoxy)-4-(11-oxo-9-phenyl-7,8,9,10,11,12-hexahydrobenzo[b][4,7]phenanthrolin-12-yl)phenyl esters of carboxylic acids were prepared by ternary condensation of vanillin or vanillal alkanoates with 6-quinolylamine and Phenidone. According to the 1H NMR spectra, the target products are formed as mixtures of diastereomers.
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