Organic Letters · 2015 · 133 citations · 40 references
Natural SciencesChemical EngineeringChemistryCatalysisInorganic ChemistryOrganic ChemistryCatalyst DesignCatalyst PreparationCatalytic MechanismsCross-coupling ReactionsHeterocycle SynthesisOrganic SynthesisMetallocene CatalysisMetallocene CatalystsMetallocene SynthesisSilylation ReactionsSubstrate ScopeSubstrate Scope ExpansionTransition Metal-catalyzed SynthesisTransition-metal-catalyzed Functionalization
Use of a rhodium catalyst with electron-rich and bulky chiral diphosphine ligands having C2-symmetry allowed efficient dehydrogenative silylation of the C(sp(2))-H bond of ferrocenes leading to chiral benzosiloloferrocenes. The substrate scope was expanded to hydrogermane and hydrosilanes having a ruthenocene backbone, which resulted in a new approach to benzosilole- and benzogermole-fused metallocenes.
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Asymmetric Catalysis with Chiral Ferrocene Ligands
Li‐Xin Dai, Tao Tu, Shu‐Li You et al. · Accounts of Chemical Research · 2003 · 579 citations