A cyclometalated iridium(III) complex containing a N ∧ C ∧ N-coordinating terdentate ligand [Ir(dpyx- N, C, N )Cl(μ-Cl)] 2 was found to be a general and highly effective catalyst for the α-alkylation of ketones and N -alkylation of amines with alcohols. In the presence of catalyst (1 mol % Ir) and base (0.2–0.5 equiv), a variety of desirable products were obtained in good yields under an air atmosphere. Notably, this research exhibited the new potential of Ir(III) complexes bearing non-Cp* ligand and will facilitate the progress of the hydrogen autotransfer process.
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Liu et al. (2017) studied this question.
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