Search results for "Catalysis"

showing 10 items of 5944 documents

The redox chemistry of gold with high-valence doped calcium oxide.

2012

chemistry.chemical_compoundValence (chemistry)ta114ChemistryInorganic chemistryDopingGeneral ChemistryGeneral MedicineCalcium oxideRedoxta116CatalysisAngewandte Chemie (International ed. in English)
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Formation of a Porous Zirconium Oxo Phosphate with a High Surface Area by a Surfactant-Assisted Synthesis

1996

chemistry.chemical_compoundZirconiumPulmonary surfactantChemistryInorganic chemistrychemistry.chemical_elementGeneral MedicineGeneral ChemistryPorosityPhosphateZirconium compoundsCatalysisAngewandte Chemie International Edition in English
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Back Cover: Promoter Activation in Δ hfq Mutants as an Efficient Tool for Specialized Metabolite Production Enabling Direct Bioactivity Testing (Ange…

2019

chemistry.chemical_compoundbiologyBiochemistryChemistryMetaboliteMutantINTCover (algebra)General ChemistryProteobacteriabiology.organism_classificationCatalysisAngewandte Chemie International Edition
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Anodic Formation of Aryl Mesylates through Dehydrogenative Coupling Reaction

2018

chemistry.chemical_compoundchemistry010405 organic chemistryArylElectrochemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysisCoupling reaction0104 chemical sciencesAnodeChemElectroChem
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Efficient and stereodivergent electrochemical synthesis of optically pure menthylamines.

2011

chemistry.chemical_compoundchemistry010405 organic chemistryOrganic chemistryGeneral Chemistry010402 general chemistryOximeElectrochemistry01 natural sciencesReductive aminationCatalysis0104 chemical sciencesAngewandte Chemie (International ed. in English)
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Asymmetric Synthesis of Five-Membered Spiropyrazolones via N-Heterocyclic Carbene (NHC)-Catalyzed [3+2] Annulations

2016

A new synthetic strategy for the asymmetric synthesis of five-membered spiropyrazolones via N-heterocyclic carbene-catalyzed [3+2] annulations employing enals and unsaturated pyrazolones as substrates has been developed. The new protocol allows the flexible variation of all four substituents of the pharmaceutically important spiropyrazolones in moderate to very good yields and in most cases with excellent diastereoselectivities and good to excellent enantioselectivities.

chemistry.chemical_compoundchemistry010405 organic chemistryStereochemistryOrganic ChemistryEnantioselective synthesisPyrazolones010402 general chemistry01 natural sciencesCarbeneCatalysis0104 chemical sciencesCatalysisSynthesis
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ChemInform Abstract: Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Rea…

2010

Several polystyrene-supported proline dipeptides and a prolinamide derivative were prepared by thiol–ene coupling. These materials were used as catalysts for the direct asymmetric aldol reaction in water, and results compared with unsupported catalysts in water. Such an approach gave more active or stereoselective catalysts compared to the unsupported compounds, showing that our immobilization procedure may be useful to develop catalytic materials with enhanced performance. Moreover, these catalysts can be recovered and reused for at least nine times without loss of activity or can be easily regenerated when their activity has decreased. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, …

chemistry.chemical_compoundchemistryAldol reactionOrganocatalysisImmobilization procedureOrganic chemistryStereoselectivityGeneral MedicinePolystyreneProlineDerivative (chemistry)CatalysisChemInform
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ChemInform Abstract: New Simple Hydrophobic Proline Derivatives as Highly Active and Stereoselective Catalysts for the Direct Asymmetric Aldol Reacti…

2009

New 4-substituted acyloxyproline derivatives with different hydrophobic properties of the acyl group were easily synthesized and used as catalysts in the direct asymmetric aldol reaction between cyclic ketones (cyclohexanone and cyclopentanone) and several substituted benzaldehydes. Reactions were carried out using water, this being the best reaction medium examined. Screening of these catalysts showed that compounds bearing the most hydrophobic acyl chains [4-phenylbutanoate and 4-(pyren-1-yl)butanoate] provided better results. The latter catalysts were successfully used in only 2 mol% at room temperature without additives to give aldol products in excellent stereoselectivities. These resu…

chemistry.chemical_compoundchemistryAldol reactionorganic chemicalsOrganocatalysisSubstituentMoietyCyclohexanoneOrganic chemistryGeneral MedicineCyclopentanoneAcyl groupCatalysisChemInform
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ChemInform Abstract: Palladium-Catalyzed Alkoxy- and Aminocarbonylation of α-Halomethyl Oxime Ethers: Synthesis of 1,3-Alkoxyimino Esters and 1,3-Alk…

2015

The three component reactions of α-bromomethyl oxime ethers, carbon monoxide, and alcohols or aromatic amines give imino esters and amides, respectively.

chemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistrychemistry.chemical_elementheterocyclic compoundsGeneral MedicineOximeCarbonylationCatalysisCarbon monoxidePalladiumChemInform
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ChemInform Abstract: Rhodium(III)-Catalyzed Ring-Opening of Strained Olefins Through C-H Activation of O-Acetyl Ketoximes: An Efficient Synthesis of …

2014

An efficient strategy for the stereoselective synthesis of functionalized cyclopentenes and spiro[2.4]heptenes from strained olefins via C–H activation of aryl ketone O-acetyl ketoximes using [RhCl2Cp∗]2 catalyst is described. The results revealed that a wide range of readily accessible aryl and heteroaryl ketoximes are compatible in this method for the ring opening of bicyclic and spirotricyclic olefins.

chemistry.chemical_compoundchemistryBicyclic moleculeArylchemistry.chemical_elementOrganic chemistryStereoselectivityGeneral MedicineAryl ketoneRing (chemistry)Medicinal chemistryRhodiumCatalysisChemInform
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