2 research outputs found

    CoCl(PPh<sub>3</sub>)<sub>3</sub> as Cyclotrimerization Catalyst for Functionalized Triynes under Mild Conditions

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    The ubiquitary Co­(I) complex CoCl­(PPh<sub>3</sub>)<sub>3</sub> was found to be a convenient catalyst for the [2 + 2 + 2] cycloaddition of functionalized triynes under mild reaction conditions and devoid of any additional additive, yielding the substituted arene compounds. Successful development of synthetic routes to various triynes and the subsequent cyclotrimerization key step gave systematic access to a variety of different bi- and triaryls with good to excellent yields for the cyclization

    Synthesis and Catalytic Activity of [Cp′Co(COD)] Complexes Bearing Pendant N‑Containing Groups

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    The novel Co­(I)-complex [Cp<sup>CN</sup>Co­(COD)] (Cp<sup>CN</sup> = η<sup>5</sup>-(C<sub>5</sub>H<sub>4</sub>CMe<sub>2</sub>CH<sub>2</sub>CN), COD = 1,5-cyclooctadiene; <b>3</b>) with a substituted cyclopentadienyl ligand containing a pendant nitrile moiety has been synthesized and characterized by X-ray diffraction. The reactivity of the nitrile group in <b>3</b> has been investigated regarding its behavior in cyclization reactions with alkynes, leading to three new complexes containing pendant 2-pyridyl groups. All synthesized complexes have been evaluated as catalysts in the [2 + 2 + 2] cycloaddition reaction of 1,6-heptadiyne and benzonitrile
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