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Direct attack of the bis(μ-oxo)dicopper core on an arene appears feasible in tyrosinase and model complexes on the basis of studies of new Cu(III) 2 (μ-O)2 (2+) compounds supported by bidentate imine/amine ligands. In the first demonstration of such reactivity for a bis(μ-oxo)dicopper core, decomposition of these intermediates caused hydroxylation of a pendant phenyl ring Eq. (a) in a reaction analogous to that catalyzed by tyrosinase.
Holland et al. (Mon,) studied this question.