sameAs
A new family of halogen-chelated Hoveyda-Grubbs-type metathesis catalysts.Advanced fine-tuning of grubbs/hoveyda olefin metathesis catalysts: a further step toward an optimum balance between antinomic properties.In an attempt to provide a user's guide to the galaxy of benzylidene, alkoxybenzylidene, and indenylidene ruthenium olefin metathesis catalysts.Sustainable concepts in olefin metathesis.Progress in metathesis chemistry.Mechanistic insights into the cis-trans isomerization of ruthenium complexes relevant to catalysis of olefin metathesis.High-Performance Isocyanide Scavengers for Use in Low-Waste Purification of Olefin Metathesis Products.A fine-tuned molybdenum hexacarbonyl/phenol initiator for alkyne metathesis.Is the Hoveyda-Grubbs complex a vinylogous Fischer-type carbene? Aromaticity-controlled activity of ruthenium metathesis catalysts.A highly active aqueous olefin metathesis catalyst bearing a quaternary ammonium group.Olefin cross-metathesis with vinyl halides.Synthesis of Selectively Substituted or Deuterated Indenes via Sequential Pd and Ru Catalysis.Well-Defined Chiral Copper NHC Complex in the Asymmetric Conjugated β-Borylation and One-Pot Metathesis-Asymmetric β-Borylation Reactions.Azoliniums, Adducts, NHCs and Azomethine Ylides: Divergence in Wanzlick Equilibrium and Olefin Metathesis Catalyst Formation.Force field parametrization and molecular dynamics simulation of flexible POSS-linked (NHC; phosphine) Ru catalytic complexes.Mild Functionalization of Tetraoxane Derivatives via Olefin Metathesis: Compatibility of Ruthenium Alkylidene Catalysts with Peroxides.Correction to "Mild Functionalization of Tetraoxane Derivatives via Olefin Metathesis: Compatibility of Ruthenium Alkylidene Catalysts with Peroxides".Aqueous olefin metathesis.Ruthenium-Amido Complexes: Synthesis, Structure, and Catalytic Activity in Olefin MetathesisThe Doping Effect of Fluorinated Aromatic Solvents on the Rate of Ruthenium-Catalysed Olefin MetathesisThe Joy and Challenge of Small Rings MetathesisProbing of the Ligand Anatomy: Effects of the Chelating Alkoxy Ligand Modifications on the Structure and Catalytic Activity of Ruthenium Carbene ComplexesHomo- and Cross-Olefin Metathesis Coupling of Vinylphosphane Oxides and Electron-Poor Alkenes: Access to P-Stereogenic DienophilesNitro-Substituted Hoveyda−Grubbs Ruthenium Carbenes: Enhancement of Catalyst Activity through Electronic ActivationOrtho- and Para-Substituted Hoveyda−Grubbs Carbenes. An Improved Synthesis of Highly Efficient Metathesis Initiators†Synthesis of SubstitutedP-Stereogenic Vinylphosphine Oxides by Olefin Cross-MetathesisRing-Closing Alkyne Metathesis: Application to the Stereoselective Total Synthesis of Prostaglandin E2-1,15-LactoneStudies on electronic effects in O-, N- and S-chelated ruthenium olefin-metathesis catalystsGold(I)-Catalyzed Formation of Naphthalene/Acenaphthene Heterocyclic AcetalsHelicenes as Chirality-Inducing Groups in Transition-Metal Catalysis: The First Helically Chiral Olefin Metathesis CatalystSequential Alkene Isomerization and Ring-Closing Metathesis in Production of Macrocyclic Musks from BiomassAt Long Last: Olefin Metathesis Macrocyclization at High ConcentrationIn a Quest for Selectivity Paired with Activity: A Ruthenium Olefin Metathesis Catalyst Bearing an Unsymmetrical Phenanthrene-Based N-Heterocyclic CarbenePreparation of Musk-Smelling Macrocyclic Lactones from Biomass: Looking for the Optimal Substrate CombinationRuthenium Complexes Bearing Thiophene-Based Unsymmetrical N-Heterocyclic Carbene Ligands as Selective Catalysts for Olefin Metathesis in Toluene and Environmentally Friendly 2-MethyltetrahydrofuranProgress in metathesis chemistryEthyl Lactate: A Green Solvent for Olefin Metathesis
P50
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P50
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Polish chemist
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Polish chemist
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Polish chemist
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Poola keemik
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ceimiceoir Polannach
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chimico polacco
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Lesław Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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Karol Grela
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0000 0003 8885 3229
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n2013064973
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1970-11-23T00:00:00Z
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lccn-n2013064973