Abstract

Two asymmetrical β-diketiminate magnesium methyl complexes [(DippArNacnac)MgMe(THF)] have been synthesized in high yields and structurally characterized via single crystal X-ray diffraction etc. Subsequently, they have been successfully employed as highly efficient catalysts in the cyanosilylation of ketones including natural products with low catalyst loading (0.2 mol %) under the solvent-free condition at room temperature. A plausible mechanism was proposed base on the corresponding stoichiometric experiments and density functional theory (DFT) calculations.

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