With N-methyl-naphthylamine 3-substituted 2-naphthol derivatives give
the corresponding spirocyclohexadienones in good yields; 9-phenanthrol
also proceeds analogously. 4-Substituted 1-naphthols react similarly
but the spiroketones thus obtained are more labile and are formed in m
inor yields. From the behavior of spirocyclohexadienones with protonic
acids, carbonyl reagents and complex hydrides a reaction mechanism is
deduced.