Search results for "reduction"

showing 10 items of 2058 documents

Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts.

2004

Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)-imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions p…

chemistry.chemical_classificationTitaniumMolecular StructureChemistryGermaniumOrganic ChemistryThioanisoleInorganic chemistryGeneral ChemistrySulfidesHeterogeneous catalysisSilicon DioxidePeroxideCatalysisCatalysischemistry.chemical_compoundPyrimidinesCatalytic oxidationIonic liquidSolventsParticle SizeTrifluoromethanesulfonateOxidation-ReductionPorosityAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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Experimental evidence for proton motive force-dependent catalysis by the diheme-containing succinate:menaquinone oxidoreductase from the Gram-positiv…

2006

In Gram-positive bacteria and other prokaryotes containing succinate:menaquinone reductases, it has previously been shown that the succinate oxidase and succinate:menaquinone reductase activities are lost when the transmembrane electrochemical proton potential, Deltap, is abolished by the rupture of the bacteria or by the addition of a protonophore. It has been proposed that the endergonic reduction of menaquinone by succinate is driven by the electrochemical proton potential. Opposite sides of the cytoplasmic membrane were envisaged to be separately involved in the binding of protons upon the reduction of menaquinone and their release upon succinate oxidation, with the two reactions linked…

chemistry.chemical_classificationbiologyProtonophoreChemiosmosisSuccinic AcidProton-Motive ForceBacillusVitamin K 2HemeReductasebiology.organism_classificationBiochemistryRedoxCatalysisSuccinate DehydrogenaseEnzymeBiochemistrychemistryBacterial ProteinsFumaratesOxidoreductaseBacillus licheniformisOxidoreductasesOxidation-ReductionBacteriaBiochemistry
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Succinate dehydrogenase functioning by a reverse redox loop mechanism and fumarate reductase in sulphate-reducing bacteria.

2006

Sulphate- or sulphur-reducing bacteria with known or draft genome sequences (Desulfovibrio vulgaris, Desulfovibrio desulfuricans G20, Desulfobacterium autotrophicum [draft], Desulfotalea psychrophila and Geobacter sulfurreducens) all contain sdhCAB or frdCAB gene clusters encoding succinate : quinone oxidoreductases. frdD or sdhD genes are missing. The presence and function of succinate dehydrogenase versus fumarate reductase was studied. Desulfovibrio desulfuricans (strain Essex 6) grew by fumarate respiration or by fumarate disproportionation, and contained fumarate reductase activity. Desulfovibrio vulgaris lacked fumarate respiration and contained succinate dehydrogenase activity. Succi…

chemistry.chemical_classificationbiologySulfatesSuccinate dehydrogenaseMolecular Sequence DataSuccinic AcidBacillus subtilisFumarate reductasebiology.organism_classificationMicrobiologySuccinate DehydrogenaseEnzymechemistryBiochemistryFumaratesMultigene Familybiology.proteinDesulfovibrioSDHDAmino Acid SequenceDesulfovibrio vulgarisGeobacter sulfurreducensOxidation-ReductionBacteriaMicrobiology (Reading, England)
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Heterogeneous salt distribution in hot snacks enhances saltiness without loss of acceptability

2013

clef UT: 000318667000026; International audience; Abstract Health issues have led worldwide organisations to encourage the food industry to reduce salt in processed foods. Therefore, different strategies for salt reduction have been investigated. Here, the effect of heterogeneous salt distribution on saltiness perception intensity was assessed to compensate for salt reduction in snack foods. Two models of hot-served baked foods were developed. One model is made of two layers that vary in composition (cream-based and cereal-based layers) and salt (NaCl) concentration; the other one is made of four cream-based layers that vary in salt concentrations. Consumer panels rated the saltiness intens…

chemistry.chemical_classificationlikingTasteFood industrybusiness.industryChemistry[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritiondigestive oral and skin physiologySalt reductionfood and beveragesSalt (chemistry)layered food productsSnack foodConsumer panelstaste enhancementFood processingheterogeneous tastant distributionFood sciencesalt reductionbusiness[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood ScienceFood Research International
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Synthesis of 1H-imidazo[3′,4′:4,5]thieno[2,3-b]pyridines. A new ring system

1984

A facile and convenient synthesis of the title compounds is described, using as starting materials the 2-nitro-3-aminothieno[2,3-b]pyridines. Mass spectral data of the above mentioned compounds are briefly discussed.

chemistry.chemical_compoundAcetic acidchemistryBicyclic moleculeFormic acidOrganic ChemistryChemical reductionOrganic chemistryImideRing (chemistry)Spectral dataJournal of Heterocyclic Chemistry
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On the electrochemical reduction of carbon dioxide and ethylene

1973

Die gemeinsame Elektrolyse von Athylen (I) und Kohlendioxid (II) liefert je nach den angewandten Bedingungen Mischungen aus Oxalsaure (III) und Bemsteinsaure (IV).

chemistry.chemical_compoundEthyleneOzoneCarbon dioxide reformingChemistryMethanizerOrganic ChemistryDrug DiscoveryBiochemistryElectrochemical reduction of carbon dioxideNuclear chemistryTetrahedron Letters
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Synthesis of Enantiopure 6,11‐Methylene Lipoxin B4Methyl Ester

2021

chemistry.chemical_compoundLuche reductionNatural productEnantiopure drugchemistryLipoxin B4Organic ChemistryConvergent synthesisTotal synthesisOrganic chemistryPhysical and Theoretical ChemistryMethyleneEuropean Journal of Organic Chemistry
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Recent Scientific and Technological Developments in Electrochemical Carboxylation Based on Carbon Dioxide

2010

chemistry.chemical_compoundMaterials scienceCarbon dioxidechemistryChemical engineeringCarboxylationGalvanic anodeCarbon dioxideInorganic chemistryElectrocatalystElectrochemistryElectrochemical reduction of carbon dioxide
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ChemInform Abstract: Electroorganic Synthesis of Nitriles via a Halogen-Free Domino Oxidation-Reduction Sequence.

2016

A direct electroorganic sequence yielding nitriles from oximes in undivided cells is reported. Despite the fact that intermediate nitrile oxides might be formed, the method is viable to prepare benzonitriles without substituents ortho to the aldoxime moiety. This constant current method is easy to perform for a broad scope of substrates and employs common electrodes, such as graphite and lead.

chemistry.chemical_compoundNitrilechemistryElectrodeMoietyHalogen freeSequence (biology)Oxidation reductionGeneral MedicineGraphiteCombinatorial chemistryDominoChemInform
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Redox properties of nitrophenylporphyrins and electrosynthesis of nitrophenyl-linked Zn porphyrin dimers or arrays

2014

Five nitrophenylporphyrins were investigated as to their electrochemical properties in CH 2 Cl 2 containing 0.1 M TBAP. The investigated compounds are represented as ( NO 2 Ph )x Ph 4-x PorM , where Por represents the dianion of the porphyrin macrocycle, Ph is a phenyl group on meso-position of the macrocycle, NO 2 Ph is a meso-substituted nitrophenyl group, M = 2 H , Pd II or Zn II and x = 1 or 2. Each porphyrin undergoes an initial one electron reduction at E1/2 = -1.07 to -1.12 V where the added negative charge is almost totally localized on the meso-nitrophenyl group of the compound. This reversible reduction is then followed by one or more irreversible reductions of the nitrophenyl an…

chemistry.chemical_compoundchemistryOne-electron reductionPhenyl groupGeneral ChemistryConjugated systemElectrosynthesisPhotochemistryElectrochemistryPorphyrinMedicinal chemistryRedoxIonJournal of Porphyrins and Phthalocyanines
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