Journal of the American Chemical Society · 2010 · 64 citations · 16 references
Natural SciencesChemistryCatalysisOrganometallic ChemistryReaction EngineeringCatalyst DesignCatalytic MaterialsCatalytic MechanismsCatalytic Reaction EngineeringCross-coupling ReactionsCatalyst Structure - Activity RelationshipsCatalyst Structure-activity RelationshipsMetathesis CatalysisMetathesis ReactionsOlefin MetathesisOlefin Metathesis CatalysisRing-closing MetathesisSteric Bulk
The relative TONs of productive and nonproductive metathesis reactions of diethyl diallylmalonate are compared for eight different ruthenium-based catalysts. Nonproductive cross metathesis is proposed to involve a chain-carrying ruthenium methylidene. A second more-challenging substrate (dimethyl allylmethylallylmalonate) that forms a trisubstituted olefin product is used to further delineate the effect of catalyst structure on the relative efficiencies of these processes. A steric model is proposed to explain the observed trends.
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