Search results for "Catalysis"

showing 10 items of 5944 documents

Front Cover: Visible Light Enables Aerobic Iodine Catalyzed Glycosylation (Eur. J. Org. Chem. 28/2019)

2019

chemistry.chemical_compoundFront coverGlycosylationchemistryOrganic Chemistrychemistry.chemical_elementPhysical and Theoretical ChemistryPhotochemistryIodineVisible spectrumCatalysisEuropean Journal of Organic Chemistry
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CdSe/ZnS Nanocrystals with Dye-Functionalized Polymer Ligands Containing Many Anchor Groups

2005

chemistry.chemical_compoundFunctionalized polymerMaterials scienceCadmium selenidechemistryNanocrystalEnergy transferInorganic chemistryPolymer chemistryGeneral ChemistryCatalysisAngewandte Chemie International Edition
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Visible Light Enables Aerobic Iodine Catalyzed Glycosylation

2019

chemistry.chemical_compoundGlycosylationCarbohydrate chemistryChemistryOrganic Chemistrychemistry.chemical_elementPhysical and Theoretical ChemistryPhotochemistryIodineCatalysisVisible spectrumEuropean Journal of Organic Chemistry
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Task Specific Dicationic Ionic Liquids: Recyclable Reaction Media for the Mononuclear Rearrangement of Heterocycles

2014

Nine functionalized dicationic ionic liquids were used to study the base catalyzed mononuclear rearrangement of (Z)-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole into the corresponding triazole at 363 K. Ionic liquids were characterized by the presence of 1-(1-imidazolylmethyl)-3,5-di[1-(3'-octylimidazolylmethyl)]benzene cation, bearing on the structure a neutral imidazole unit as basic functionality. Besides anions generally used for monocationic ionic liquids, such as [Br(-)], [BF4(-)], and [NTf2(-)], also dianions having a rigid aromatic spacer such as 1,4-benzenedicarboxylate, 2,6-naphthalenedicarboxylate, and 1,5- and 2,6-naphthalenedisulfonate were taken into account. Further…

chemistry.chemical_compoundGreen chemistrychemistryOrganic ChemistryIonic liquidPolymer chemistryTriazoleImidazoleOrganic chemistrySettore CHIM/06 - Chimica OrganicaIonic liquidBenzeneCatalysisThe Journal of Organic Chemistry
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Asymmetric Aldol Reaction with Polystyrene-Supported Proline-Based Catalysts

2009

chemistry.chemical_compoundHajos–Parrish–Eder–Sauer–Wiechert reactionNitroaldol reactionAldol reactionchemistryOrganocatalysisOrganocatalysis proline supported-catalysts aldol reaction proline peptidesOrganic chemistryAldol condensationSettore CHIM/06 - Chimica OrganicaPolystyreneProlineLewis acid catalysisSynfacts
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Asymmetric aldol reaction in water catalyzed by polystyrene-supported proline

2007

chemistry.chemical_compoundHajos–Parrish–Eder–Sauer–Wiechert reactionchemistryAldol reactionOrganocatalysisOrganic chemistryPolystyreneProlineSettore CHIM/06 - Chimica OrganicaSupported organocatalystCatalysis
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ChemInform Abstract: Imidazolium and Potassium Hydrogen Carbonate Salts as Ecofriendly Organocatalysts for Oxazolidinone Synthesis.

2016

Although oxazolidinones are valuable intermediate compounds for industrial applications, no synthetic method is suitable for their production on a large scale owing to the use of reagents/catalysts that are hazardous or toxic to human health or ecotoxic for the environment. In this manuscript, we describe new and efficient catalysts, that is, the nontoxic hydrogen carbonate anion in combination with a potassium or diisobutylimidazolium ([iBu(2)IM]) countercation, for the conversion of -amino alcohols into cyclic oxazolidinones in high yields of 69 to 90%. Depending on the catalytic conditions, both catalysts could be easily recovered from the crude reaction products and reused several times…

chemistry.chemical_compoundHuman healthHydrogenchemistryOrganocatalysisReagentPotassiumchemistry.chemical_elementCarbonateOrganic chemistryGeneral MedicineCarbonCatalysisChemInform
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Polycondensed nitrogen heterocycles. Part25. Aminopyrrolo[1,2-f]-phenanthridines by decomposition of 2-(3-azidophenyl)-1-arylpyrroles

1994

Acid catalyzed decomposition of the azido derivatives 4a-c gave rise to amino-hydroxy-phenylpyrroles of type 7 and 8 upon hydrolysis of the intermediate aryl nitrenium ions, together with the hydrogen abstraction compounds of type 3. The aminopyrrolo[1,2-f]phenanthridines 10, 11, and 12 were obtained by treatment with TFMSA of the azide 4d in which the ring being attacked was made more nucleophilic by the introduction of the methoxy group.

chemistry.chemical_compoundHydrolysisAcid catalysischemistryNucleophileArylOrganic ChemistryOrganic chemistryAzideHydrogen atom abstractionRing (chemistry)DecompositionMedicinal chemistryJournal of Heterocyclic Chemistry
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“Nonsolvent” Applications of Ionic Liquids in Organocatalysis

2012

This chapter is organized in three sections (see Figure 10.1 ): 2. Immobilization of ionic liquids and organocatalysts 2.1 Covalently attached “ ionic liquid ” moieties as supports 2.2 Covalently attached “ ionic liquid ” moieties as linkers 2.3 Covalently attached “ ionic liquid ” moieties as organocatalysts

chemistry.chemical_compoundIonic Liquids Organocatalysis Green Chemistry Asymmetric synthesischemistryOrganocatalysisIonic liquidOrganic chemistrySettore CHIM/06 - Chimica Organica
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Electrochemical Synthesis of Aryl Methoxymethyl Ethers

2019

chemistry.chemical_compoundKolbe electrolysischemistryDecarboxylationArylElectrochemistryOrganic chemistryElectrochemistryCatalysisChemElectroChem
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