Metallacyclische Acyl-carboxylate des Nickels: Reaktivitaet der Acylgruppe und Synthesepotential bei Kreuzkopplungsreaktionen mit Alkylhalogeniden

Article abstract of DOI:10.1016/0022-328X(93)80282-G

2-Cyclohexene-1,2-dicarboxylic acid-anhydride reacts with electron-rich nickel(0) centres to form nickel(0) complexes, whereas the isomeric 4-cyclohexene-1,2-dicarboxylic acid-anhydride reacts with ring opening of the anhydride to yield thermally stable acyl-carboxylato-nickel(II) compounds.The structure of a typical compound with (TMED)Ni⁰ as a complex fragment was determined by single crystal X-ray structural analysis, the crystal also containing the product of CO-elimination, the nickelalactone.The cross-coupling reaction of metallacyclic acyl-carboxylato complexes of Ni with R-X can be used for the formation of side chains of steroids containing γ-ketocarboxylic acids.These compounds are interesting precursors for the preparation of analogues of vitamin D3 metabolites.