Facile palladium-catalyzed cyclizations of arylaminoquinones giving biologi
cally important carbazoloquinones in high yields have, been performed with
oxygen as the single oxidant. By a slight modification of the catalyst, dip
henylamine, diphenyl ether, and related compounds can be cyclized. The syst
em could also be used in intermolecular couplings between naphthoquinones a
nd benzene or naphthalene.