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A simple coordination complex of uranium(III), a uranium tris(amide), can selectively couple gaseous CO to the linear ynediolate OCCO2− dianion, at room temperature and pressure, regardless of the reagent stoichiometry. This product exhibits further reactivity upon warming in the form of the addition of a C–H bond of a methyl group across the CC triple bond, this second carbon–carbon bond forming reaction generating a functionalised enediolate dianion.
Arnold et al. (Thu,) studied this question.