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Selective Linear Coupling Reaction of Acetylene and Acrylonitrile Catalyzed by the Well-Defined Metallacyclopentadiene Complex C<sub>5</sub>Me<sub>5</sub>(PPh<sub>3</sub>)(Cl)RuCHCHCHCH
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Citations
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References
1998
Year
Materials ScienceInorganic ChemistryChemical EngineeringCross-coupling ReactionSubsequent InsertionEngineeringHeterocyclicAlkene MetathesisOrganic ChemistryAcrylonitrile CatalyzedOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryInitial Pph3 Dissociation
The metallacyclopentadiene was found to catalyze the linear coupling reaction of acetylene and acrylonitrile to give predominantly 2(E),4(Z),6-heptatrienenitrile (3; TON = 15, 85% selectivity). The coupling reaction is proposed to occur via an initial PPh3 dissociation from 1 and the subsequent insertion of acrylonitrile.
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