The Povarov reaction is a well-known organic reaction that involves the formation of a tetrahydroquinoline (THQ) ring system. This reaction often proceeds via the condensation of an imine, an alkene, and an arene under acid-catalyzed or other conditions. In your case, it's performed with enecarbamates, which are likely the alkene component in the reaction.
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benzyl (E/Z)-prop-1-enylcarbamate
benzyl ((E)-2-((2S,4R)-6-methoxy-2-(naphthalen-2-yl)-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate
(2-ethyl-6-methoxy-3-methyl-1,2,3,4-tetrahydro-quinolin-4-yl)-(4-methoxy-phenyl)-amine
