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A Ni(II) complex of the Schiff base of glycine with o-[N-α-picolylamino]benzophenone or -acetophenone as a nucleophilic glycine equivalent, and N-trans-enoyloxazolidinones, as a derivative of an α,β-unsaturated carboxylic acid, were found to be the substrates of choice in the corresponding Michael addition reactions. The reactions proceed at room temperature in the presence of catalytic amounts of...
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