Beilstein Journal of Organic Chemistry · 2012 · 51 citations · 38 references
Natural SciencesChemistryCatalysisComputational ChemistryOrganic ChemistryAcid-base CatalysisCation RecognitionAcyl Transfer ReactionsElectrophilic CatalysisElectrophilic ReactivityLewis Acid CatalysisLewis Acid-base TheoryLewis Acidity
Using selected theoretical methods the affinity of a large range of Lewis bases towards model cations has been quantified. The range of model cations includes the methyl cation as the smallest carbon-centered electrophile, the benzhydryl and trityl cations as models for electrophilic substrates encountered in Lewis base-catalyzed synthetic procedures, and the acetyl cation as a substrate model for acyl-transfer reactions. Affinities towards these cationic electrophiles are complemented by data for Lewis-base addition to Michael acceptors as prototypical neutral electrophiles.
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Lewis Base Catalysis in Organic Synthesis
Scott E. Denmark, Gregory L. Beutner · Angewandte Chemie International Edition · 2008 · 1.2K citations
Efficiency in Nonenzymatic Kinetic Resolution
Edwin Vedējs, Māra Jure · Angewandte Chemie International Edition · 2005 · 741 citations