The Journal of Organic Chemistry · 2006 · 143 citations · 27 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsCatalytic Reaction EngineeringMicrowave-assisted SynthesisArylation ReactionsAtom-economic SynthesisCatalytic Reaction MechanismsMicrowave-assisted AlkylationMicrowave-assisted CatalysisMicrowave-assisted Organic SynthesisMicrowave-assisted Solvent-free SynthesisOrganometallic Catalysis
Our objectives were to develop catalytic atom-economic processes accessing and/or incorporating versatile functionality using aryl/heteroaryl acetonitriles as substrates. We report essentially solvent-free [Cp*IrCl2]2 catalyzed redox neutral processes whereby substituted acetonitriles react with primary alcohols to deliver monosubstituted aryl/heteroaryl acetonitriles in excellent yield. We further demonstrate that such processes can be achieved by conventional or microwave heating and that bis- and tris-primary alcohols are also processed efficiently.
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Microwave assisted organic reactions
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Solvent-free organic syntheses
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