Search results for "Friedel−Crafts reaction"

showing 2 items of 2 documents

Organocatalytic Enantioselective Friedel–Crafts Aminoalkylation of Indoles in the Carbocyclic Ring

2016

The first general catalytic method for the, so far elusive, enantioselective Friedel−Crafts functionalization of indoles in the carbocyclic ring is presented. This transformation contrasts with the usual tendency of these heterocycles to react at the azole ring. For this purpose, the four regioisomeric hydroxy carbocyclic-substituted indoles were reacted with several isatinderived ketimines, using a Cinchona alkaloid-based squaramide, in a low 0.5−5 mol % catalyst loading, as a bifunctional catalyst. This methodology allows the functionalization of indoles in every position of the carbocyclic ring in a regio- and enantioselective fashion, by switching only the position of the hydroxy group …

IndolesIsatin-derived ketiminesCinchona010402 general chemistryRing (chemistry)01 natural sciencesCatalysisReductive eliminationFriedel−Crafts reactionPhenolsAsymmetric catalysisOrganic chemistryFriedel–Crafts reactionbiologyOrganocatalysis010405 organic chemistryChemistrySquaramideEnantioselective synthesisQuímicaGeneral Chemistrybiology.organism_classification0104 chemical sciencesBifunctional catalystFISICA APLICADAOrganocatalysisACS Catalysis
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Acid Catalysis with Alkane/Water Microdroplets in Ionic Liquids

2021

Ionic liquids are composed of an organic cation and a highly delocalized perfluorinated anion, which remain tight to each other and neutral across the extended liquid framework. Here we show that n-alkanes in millimolar amounts enable a sufficient ion charge separation to release the innate acidity of the ionic liquid and catalyze the industrially relevant alkylation of phenol, after generating homogeneous, self-stabilized, and surfactant-free microdroplets (1–5 μm). This extremely mild and simple protocol circumvents any external additive or potential ionic liquid degradation and can be extended to water, which spontaneously generates microdroplets (ca. 3 μm) and catalyzes Brönsted rather …

UNESCO::QUÍMICAInorganic chemistryAlkylation010402 general chemistry:QUÍMICA [UNESCO]01 natural sciencesArticleIonCatalysisAcid catalysischemistry.chemical_compoundFriedel−Crafts reactionMicroemulsionLewis acids and basesFriedel-Crafts reactionQD1-999Alkanechemistry.chemical_classification010405 organic chemistryWater microdropletsAlkane microemulsionsIonic liquids3. Good health0104 chemical sciencesAcid catalysisChemistrychemistryIonic liquidddc:547JACS Au
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