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Aluminum Triflate as a Highly Active and Efficient Nonprotic Cocatalyst in the Palladium‐Catalyzed Methoxycarbonylation Reaction
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Citations
24
References
2007
Year
Materials ScienceTraditional AcidsChemical EngineeringPalladium‐catalyzed Methoxycarbonylation ReactionEngineeringCatalytic ApplicationHeterogeneous CatalysisLinear/branched Ester SelectivityOrganic ChemistryCatalysisChemistryAcid CocatalystsCatalyst PreparationAluminum TriflateCatalytic SynthesisHighly Active
Lewis does it better: Aluminum triflate readily replaces Brønsted acid cocatalysts in the palladium-catalyzed methoxycarbonylation reaction of styrene and 1-pentene, producing catalysts that are stable and more active than those using traditional acids. Catalyst loadings of 0.02 % allow conversions of up to 100 % to be achieved within three hours with no loss of linear/branched ester selectivity.
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