Abstract
The reaction between N-arylidene-2-naphthylamines and allylacetone leads to the formation of 1,3-disubstituted benzo[f]quinolines having a butenyl radical in position 1. It is shown that the reaction proceeds via intermediate aminoketones — 1-(2-naphthylamine)-1-aryl-6-heptene-3-ones.
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