Search results for "Reduction"

showing 10 items of 2058 documents

Potential Roles of Peroxisomes in Alzheimer's Disease and in Dementia of the Alzheimer's Type

2012

In Alzheimer's disease (AD) and dementia of the Alzheimer's type (DAT), the role played by peroxisomes is not well known. Peroxisomes are present in all eukaryotic cells, with the exception of erythrocytes. They are involved in the β-oxidation process of long-chain fatty acids, very-long-chain fatty acids, and branched-chain fatty acids. They participate in the α-oxidation of phytanic acid, the biosynthesis of bile acids, and the breakdown of eicosanoids. Peroxisomes are also involved in the synthesis of specific fatty acids such as docosahexaenoic acid (DHA), which is essential for the brain and retina, and plasmalogens (PLGN), which play crucial roles in neural cells and are essential com…

carnitine-dependent enzymesPhytanic acidalzheimerplasmalogenMitochondrionBiologyfatty acidsModels Biologicaldhachemistry.chemical_compoundAlzheimer Diseaselipid metabolismPeroxisomesmedicineAnimalsHumansDementianeurodegenerative diseasesperoxisomeCarnitineCognitive declineNeuronsGeneral NeuroscienceBrainGeneral MedicineMetabolismPeroxisomemedicine.diseaseMitochondriaalzheimer; fatty acids; peroxisomes; alzheimer's disease; plasmalogen; dementia; neurodegenerative diseases; dha; peroxisome; lipid metabolism; carnitine-dependent enzymesPsychiatry and Mental healthClinical PsychologychemistryBiochemistryDocosahexaenoic acidalzheimer's diseaseGeriatrics and GerontologyOxidation-Reductiondementiamedicine.drugJournal of Alzheimer's Disease
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Selective Acrolein Hydrogenation over Ligand-Protected Gold Clusters : A Venus Flytrap Mechanism

2022

The catalytic partial hydrogenation of α,β-unsaturated aldehydes is an ideal reaction to understand the selectivity between two different functional groups Here the two functional groups are C═C and C═O, and the hydrogenation of C═O is preferentially desired due to the importance of the issuing products, unsaturated alcohols, in fine-chemical industries. Using density functional theory calculations, we investigate the catalytic competency toward this reaction of a Au nanocluster in the presence of protecting ligands that offer higher stability and the possibility for the uniform distribution of size-selected clusters in the catalytic system. meta-Mercaptobenzoic-acid-protected-protected Au …

catalysistiheysfunktionaaliteoriananoclusterspelkistysnanoklusteritGeneral ChemistrygoldCatalysiskultamonolayer-protected clusterskatalyytitacrolein reductionkatalyysinanohiukkasethydrausdensity functional theory
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Effect of Pre-Reduction on the Properties and the Catalytic Activity of Pd/Carbon Catalysts: A Comparison with Pd/Al2O3

2013

The effect of pre-reduction in solution with chemical reagents on the catalytic performance and catalyst properties of Pd/carbon catalysts was systematically investigated with a multitechnique approach. The results are critically discussed in comparison to those recently obtained on analogous Pd/alumina catalysts. It was proved that the Pd phase on the carbon surface is characterized by a high mobility, opposite to what occurs on alumina. As a result, the Pd particles on carbon aggregate together during pre-reduction, with a consequent decrease in available metal surface. Pd particles remain aggregated also in reaction conditions; the decreased Pd dispersion negatively affects the catalyst …

characterization techniqueCO chemisorptionInorganic chemistryPd-based catalystchemistry.chemical_elementTPRHeterogeneous catalysisPd/CarbonCatalysisCatalysisMetalCharacterization techniquesCatalyst pre-reductionTemperature-programmed reductionX-ray absorption spectroscopymetal nanoparticlein situPd-based catalystsPd/aluminaSAXSGeneral ChemistryXANESSmall Angle X-ray ScatteringX-ray Absorption SpectroscopyPd/Carbon; Pd/alumina; metal nanoparticle; catalysis; Catalyst pre-reduction; in situ; SAXS; XANES; Pd-based catalysts; heterogeneous catalysis; Characterization techniques; Temperature-programmed reduction; TPR; CO chemisorption; TEM; X-ray absorption spectroscopy; Small Angle X-ray Scatteringheterogeneous catalysischemistryReagentvisual_arttemperature-programmed reductionvisual_art.visual_art_mediumTEMheterogeneous catalysiSmall Angle X-ray SpectroscopyDispersion (chemistry)Carbon
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First Highly Diastereoselective Synthesis of syn α-Methyl β-Fluoroalkyl β-Amino Esters

1999

A new two-step approach for the diastereoselective synthesis of the syn α-methyl β-fluoroalkyl β-amino esters 4 has been developed. This approach is based on the chemical reduction of the fluorinated β-enamino esters 3, which have been previously obtained from imidoyl chlorides 1 and lithium ester enolates, with ZnI2/NaBH4 as the reducing agent. The process takes place with high syn diastereoselectivity and good to excellent yields. A metal-chelated six-membered model has been suggested to explain the stereochemical outcome of the reduction reaction.

chemistryAmino estersReducing agentOrganic ChemistryChemical reductionchemistry.chemical_elementLithiumPhysical and Theoretical ChemistryBiochemistryMedicinal chemistryRedoxOrganic Letters
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Relationship between Electron Affinity and Half-Wave Reduction Potential: A Theoretical Study on Cyclic Electron-Acceptor Compounds.

2016

A high-level ab initio protocol to compute accurate electron affinities and half-wave reduction potentials is presented and applied for a series of electron-acceptor compounds with potential interest in organic electronics and redox flow batteries. The comprehensive comparison between the theoretical and experimental electron affinities not only proves the reliability of the theoretical G3(MP2) approach employed but also calls into question certain experimental measurements, which need to be revised. By using the thermodynamic cycle for the one-electron attachment reaction A+e- →A- , theoretical estimates for the first half-wave reduction potential have been computed along the series of ele…

chemistry.chemical_classification010304 chemical physicsChemistryAb initioSolvationElectronElectron acceptor010402 general chemistry01 natural sciencesRedoxAtomic and Molecular Physics and Optics0104 chemical sciencesReduction (complexity)Ab initio quantum chemistry methodsComputational chemistryChemical physicsElectron affinity0103 physical sciencesPhysical and Theoretical ChemistryChemphyschem : a European journal of chemical physics and physical chemistry
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Selective isomerization of a trans -butanediacetal derivative of tartaric acid with differentiating substituents at C-2 and C-3

2017

Abstract A trans-disubstituted butanediacetal derivative with two different substituents (ester and thioester) – methyl (2R,3R,5R,6R)-3-ethylsulfanylcarbonyl-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2-carboxylate, was selectively converted to the cis derivative – methyl (2S,3R,5R,6R)-3-ethylsulfanylcarbonyl-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2-carboxylate in high yield on a multigram scale. The product of this reaction offers the possibility for selective modification of one of the substituents, which was demonstrated by Fukuyama reduction of the thioester group.

chemistry.chemical_classification010405 organic chemistryStereochemistryOrganic Chemistryenolateselective isomerization010402 general chemistryThioester01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundFukuyama reductionbutanediacetalschemistryYield (chemistry)Drug DiscoveryTartaric acidFukuyama reductionIsomerizationDerivative (chemistry)Tetrahedron Letters
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Redox Biochemistry of the Genetic Code.

2021

New findings on the chemistry of the amino acids, their role in protein folding, and their sequential primordial introduction have uncovered concealed causalities in genetic code evolution. The genetically encoded amino acids successively provided (i) membrane anchors, (ii) halophilic protein folds, (iii) mesophilic protein folds, (iv) metal ligation, and (v) antioxidation.

chemistry.chemical_classification0303 health sciencesModels GeneticChemistryProteinsGenetic codeBiochemistryRedoxHalophileEnzyme catalysisAmino acidEvolution Molecular03 medical and health sciences0302 clinical medicineBiochemistryAbiogenesisGenetic CodeProtein foldingAmino AcidsMolecular BiologyOxidation-Reduction030217 neurology & neurosurgery030304 developmental biologyTrends in biochemical sciences
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Nickel‐Mediated Photoreductive Cross Coupling of Carboxylic Acid Derivatives for Ketone Synthesis**

2021

A simple photochemical, nickel-catalyzed synthesis of ketones starting from carboxylic acids is presented. Hantzsch-ester (HE) functions as a cheap, green and strong photoreductant upon visible-light excitation to facilitate radical generation and also engages in the Ni-catalytic cycle to restore the reactive species. With this dual role, HE allows for the coupling of a large variety of radicals (1°,2°, benzylic, α-oxy & α-amino) with aroyl and alkanoyl moieties, a new feature in the synthesis of ketones through dual nickel photoredox catalysis. With both precursors deriving from abundant carboxylic acids, this protocol is a welcome addition to the organic chemistry toolbox. The reactio…

chemistry.chemical_classification540 Chemistry and allied sciencesRadicalCarboxylic acidOrganic ChemistryKetone synthesisCarboxylic AcidsPhotoredox catalysischemistry.chemical_elementGeneral ChemistryKetonesCombinatorial chemistryCatalysisMetalCoupling (electronics)NickelchemistryNickel540 ChemieReagentvisual_artvisual_art.visual_art_mediumPhotocatalysisOxidation-ReductionChemistry – A European Journal
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Observations on the use of a sulfuric acid medium for As(V) to As(III) reduction in lodimetric titrations: Application to the determination of total …

1991

Abstract The use of a sulfuric rather than a hydrochloric acid medium for the reduction of As(V) to As(III) by iodide is proposed. Optimum conditions of acid concentration, amount of sodium hydroxide, and time and temperature are established to achieve quantitative reduction. The optimized reduction procedure was applied to the iodimetric determination of total arsenic and compared to a procedure that employs a hydrochloric acid medium. A systematic error of 0.04% was found for the method with a sulfuric acid medium opposed to 0.05% for the method with a hydrochloric acid medium in the reduction step. The proposed modified iodimetric method has been successfully used with some organic sampl…

chemistry.chemical_classificationAcid concentrationIodideInorganic chemistrychemistry.chemical_elementHydrochloric acidSulfuric acidAnalytical ChemistryReduction (complexity)chemistry.chemical_compoundchemistrySodium hydroxideTitrationSpectroscopyArsenicMicrochemical Journal
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Identification and structural characterization of O-beta-ribosyl-(1"----2')-adenosine-5"-phosphate in yeast methionine initiator tRNA.

1990

We report in this paper on the complete structure determination of the modified nucleotide A*, now called Ar(p), that was previously identified in yeast methionine initiator tRNA as an isomeric form of O-ribosyl-adenosine bearing an additional phosphoryl-monoester group on its ribose2 moiety. By using the chemical procedure of periodate oxidation and subsequent beta-elimination with cyclohexylamine on mono- and dinucleotides containing Ar(p), we characterized the location of the phosphate group on the C-5" of the ribose2 moiety, and the linkage between the two riboses as a (1"----2')-glycosidic bond. Since the structural difference between phosphatase treated Ar(p) and authentic O-alpha-rib…

chemistry.chemical_classificationAdenosine monophosphateMethionineRNA Transfer MetStereochemistryChemical structurePhosphataseCyclohexylamineSaccharomyces cerevisiaeBiologyAdenosine Monophosphatechemistry.chemical_compoundchemistryBiochemistryTransfer RNAGeneticsMoietyNucleotideIndicators and ReagentsOxidation-ReductionChromatography High Pressure LiquidNucleic acids research
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