Abstract
The comparative reactivities of 6-amino-1,2,3-trimethyl- and 6-amino-7-methoxy-2,3-dimethylindoles with acetylacetone, dibenzoylmethane, and with aceto- and trifluoroacetoacetic esters have been studied. Methods have been developed for the preparation of some functionally substituted pyrrolo-[3,2-g]quinolines.
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