Journal of the American Chemical Society · 2006 · 146 citations · 23 references
Natural SciencesChemical EngineeringChemistryCatalysisOrganic ChemistryReaction EngineeringCatalyst DesignCatalyst PreparationCatalyst StabilityCatalyst SynthesisCatalytic MaterialsCatalytic MechanismsCatalytic Reaction MechanismsElectron-withdrawing GroupsFine-tuningInitiationMetathesis CatalysisMetathesis ReactionsOlefin MetathesisOlefin Metathesis Catalysis
A 95% yield in the cross metathesis of acrylonitrile with a model olefin is achieved at 25 degrees C with only 3 mol % of the new air-stable ruthenium catalyst 1f shown in the enclosed structural diagram. Even more remarkable are the performances of its boosted version 1g incorporating an electron-withdrawing group. Both these new enhanced versions of Hoveyda catalyst are readily available from Grubbs second generation precatalyst upon reaction with a styrenyl ether the end group of which has been functionalized by an ester function. The latter acts as a weakly coordinating ligand allowing to reach a desirable balance between antinomic properties such as the catalyst's stability, a high activity for challenging substrates, and a high initiation rate.
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Metathesis Reactions in Total Synthesis
K. C. Nicolaou, Paul G. Bulger, David Šarlah · Angewandte Chemie International Edition · 2005 · 1.2K citations