Journal of the American Chemical Society · 2000 · 2K citations · 18 references
Natural SciencesChemical EngineeringChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsHeterocycle SynthesisHeterocyclic ChemistryCatalytic ActivityCatalytic Activity EnhancementHeterocyclic CatalystsHeterocyclic LigandsMetathesis CatalysisOlefin MetathesisOlefin Metathesis CatalysisRing-closing Metathesis
Several highly active, recoverable and recyclable Ru-based metathesis catalysts are presented. The crystal structure of Ru complex 5, bearing a 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene and styrenyl ether ligand is disclosed. The heterocyclic ligand significantly enhances the catalytic activity, and the styrenyl ether allows for the easy recovery of the Ru complex. Catalyst 5 promotes ring-closing metathesis (RCM) and the efficient formation of various trisubstituted olefins at ambient temperature in high yield within 2 h; the catalyst is obtained in >95% yield after silica gel chromatography and can be used directly in subsequent reactions. Tetrasubstituted olefins can also be synthesized by RCM reactions catalyzed by 5 . In addition, the synthesis and catalytic activities of two dendritic and recyclable Ru-based complexes are disclosed ( 32 and 33 ). Examples involving catalytic ring-closing, ring-opening, and cross metatheses are presented where, unlike monomer 5, dendritic 33 can be readily recovered.
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Peter Schwab, Robert H. Grubbs, Joseph W. Ziller · Journal of the American Chemical Society · 1996 · 2.1K citations
Peter Schwab, Marcia B. France, Joseph W. Ziller et al. · Angewandte Chemie International Edition in English · 1995 · 1.5K citations
A Recyclable Ru-Based Metathesis Catalyst
Jason S. Kingsbury, Joseph P. A. Harrity, Peter J. Bonitatibus et al. · Journal of the American Chemical Society · 1999 · 938 citations