Search results for "carboxylation"

showing 10 items of 81 documents

Enantioselective Mannich reaction of β-keto esters with aromatic and aliphatic imines using a cooperatively assisted bifunctional catalyst

2014

An efficient urea-enhanced thiourea catalyst enables the enantioselective Mannich reaction between β-keto esters and N-Boc-protected imines under mild conditions and minimal catalyst loading (1–3 mol %). Aliphatic and aromatic substituents are tolerated on both reaction partners, affording the products in good enantiomeric purity. The corresponding β-amino ketones can readily be accessed via decarboxylation without loss of enantiomeric purity.

Molecular StructureChemistryDecarboxylationOrganic ChemistryEnantioselective synthesisThioureaEstersStereoisomerismKetonesBiochemistryDecarboxylationCatalysisCatalysisBifunctional catalystchemistry.chemical_compoundThioureaOrganic chemistryUreaIminesPhysical and Theoretical ChemistryEnantiomerMannich reactionta116Organic Letters
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Oxidative decarboxylation of naproxen.

1992

The decarboxylation of naproxen (1H) and its salt (1-) was achieved by means of chemical [Ce(IV) or S2O8(2-)] and electrochemical oxidation. The product patterns were compatible with mechanisms involving single-electron transfer from the pi-system or the carboxylate moiety. The results are discussed in connection with the involvement of electron-transfer processes in the reported phototoxicity of naproxen.

NaproxenChemistryDecarboxylationPharmaceutical ScienceElectrochemistryOxidantsMedicinal chemistrychemistry.chemical_compoundNaproxenmedicineElectrochemistrySolventsOrganic chemistryMoietyChemical stabilityCarboxylatePhototoxicityOxidation-ReductionOxidative decarboxylationmedicine.drugJournal of pharmaceutical sciences
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Catalytic aerobic oxidative decarboxylation of α-hydroxy-acids. Methyl mandelate as a benzoyl anion equivalent

1998

Abstract The monomeric square-planar cobalt(III) complex of bis- N,N ′-disubstituted oxamides catalyses the oxidative decarboxylation of α-hydroxy acids with molecular oxygen/pivalaldehyde with very good yields. This reaction offers an interesting alternative in the use of methyl mandelate as a convenient benzoyl anion equivalent.

Organic Chemistrychemistry.chemical_elementMethyl mandelateBiochemistryIonCatalysischemistry.chemical_compoundMonomerchemistryDrug DiscoveryOrganic chemistryMolecular oxygenCobaltOxidative decarboxylationTetrahedron Letters
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Die Umsetzung von L-Äpfelsäure durchSaccharomyces cerevisiae bei der Gärung

1970

Yeasts of the genusSaccharomyces are able to decompose L-malic acid partially, during and after fermentation, whereby ethanol and carbon dioxide are the end products. The decarboxylation of malic acid by yeast can be achieved with resting cells and cell free extracts.

PharmacologyEthanolbiologyDecarboxylationfungiSaccharomyces cerevisiaefood and beveragesCell Biologybiology.organism_classificationDecompositionYeastCellular and Molecular Neurosciencechemistry.chemical_compoundchemistryBiochemistryCarbon dioxideMolecular MedicineFermentationMalic acidMolecular BiologyExperientia
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Ketorolac beats ketoprofen: lower photodecarboxylation, photohemolysis and phototoxicity

2013

Ketorolac shows reduced photohemolytic activity and low phototoxicity against human skin fibroblasts when compared to ketoprofen. The low decarboxylation quantum yield together with the efficient non-radiative deactivation of the triplet and singlet excited states of ketorolac are believed to be responsible for this behaviour.

PharmacologyKetoprofenDecarboxylationChemistryOrganic ChemistryPharmaceutical ScienceQuantum yieldHuman skinPharmacologyPhotochemistryBiochemistryKetorolacExcited stateDrug DiscoverymedicineMolecular MedicineSinglet statePhototoxicitymedicine.drugMedChemComm
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Zur Wirkung von Butazolidin im Intermedi�rstoffwechsel

1956

Butazolidin (Phenylbutazone) inhibits the oxidative decarboxylation of pyruvate and α-ketoglutarate in a final concentration of 10 mg-% (3,24 · 10−4 m). Data are presented suggesting that the β-ketothiolase is inhibited. The following enzymes or enzyme systems are not inhibited: The enzymes of the respiratory chain, the enzymes of the citric acid cycle with exception of α-ketoglutaric oxidase, the glycolysis of hexosediphosphate (slight inhibition), acetate thiokinase, sulfanilamid transacetylase, pyruvic decarboxylase from yeast, arginase, xanthine oxidase, and D-amino acid oxidase.

Pharmacologychemistry.chemical_classificationOxidase testRespiratory chainGeneral MedicineCitric acid cyclechemistry.chemical_compoundEnzymechemistryBiochemistryAcetate thiokinaseXanthine oxidaseOxidative decarboxylationPyruvate decarboxylaseNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Regional differences of substrate oxidation capacity in rat hearts: effects of extra load and endurance training.

1990

Male rats, aged 17 weeks at the end of experiments, were divided into four groups. Two groups lived in normal cage conditions with or without extra load (20% of the body weight) and two groups were trained by running with or without extra load for 8 weeks. Oxidation rates of succinate, glutamate + malate, palmitoylcarnitine, and pyruvate, and the activities of lactate dehydrogenase, citrate synthase, isocitrate dehydrogenase and cytochrome oxidase were measured in homogenates of the right ventricle and in those of the subendocardial and subepicardial layers of the left ventricle. Oxidation rates of succinate and palmitoylcarnitine tended to be higher in the subendocardium than in the subepi…

Pyruvate decarboxylationMalemedicine.medical_specialtyPhysiologyPhysical exerciseCitrate (si)-Synthasechemistry.chemical_compoundEndurance trainingPhysiology (medical)Lactate dehydrogenaseInternal medicinePhysical Conditioning AnimalmedicineCitrate synthaseCytochrome c oxidaseAnimalsPalmitoylcarnitinebiologyMusclesMyocardiumBody WeightRats Inbred StrainsRatsmedicine.anatomical_structureEndocrinologychemistryVentriclebiology.proteinPhysical EnduranceCardiology and Cardiovascular MedicineEnergy MetabolismOxidation-ReductionBasic research in cardiology
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Pyruvate kinase type M2: a crossroad in the tumor metabolome.

2002

Cell proliferation is a process that consumes large amounts of energy. A reduction in the nutrient supply can lead to cell death by ATP depletion, if cell proliferation is not limited. A key sensor for this regulation is the glycolytic enzyme pyruvate kinase, which determines whether glucose carbons are channelled to synthetic processes or used for glycolytic energy production. In unicellular organisms pyruvate kinase is regulated by ATP, ADP and AMP, by ribose 5-P, the precursor of the nucleic acid synthesis, and by the glycolytic intermediate fructose 1,6-P2 (FBP), thereby adapting cell proliferation to nutrient supply. The mammalian pyruvate kinase isoenzyme type M2 (M2-PK) displays the …

Pyruvate decarboxylationNutrition and DieteticsPyruvate dehydrogenase kinaseFatty AcidsPyruvate KinaseMedicine (miscellaneous)Glutamic AcidPyruvate dehydrogenase phosphataseBiologyPKM2Pyruvate dehydrogenase complexPyruvate carboxylaseNeoplasm ProteinsBiochemistryNeoplasmsAnimalsHumansGlycolysisPyruvate kinaseCell DivisionHydrogenThe British journal of nutrition
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Pyruvate fermentation by Oenococcus oeni and Leuconostoc mesenteroides and role of pyruvate dehydrogenase in anaerobic fermentation.

2005

ABSTRACT The heterofermentative lactic acid bacteria Oenococcus oeni and Leuconostoc mesenteroides are able to grow by fermentation of pyruvate as the carbon source (2 pyruvate → 1 lactate + 1 acetate + 1 CO 2 ). The growth yields amount to 4.0 and 5.3 g (dry weight)/mol of pyruvate, respectively, suggesting formation of 0.5 mol ATP/mol pyruvate. Pyruvate is oxidatively decarboxylated by pyruvate dehydrogenase to acetyl coenzyme A, which is then converted to acetate, yielding 1 mol of ATP. For NADH reoxidation, one further pyruvate molecule is reduced to lactate. The enzymes of the pathway were present after growth on pyruvate, and genome analysis showed the presence of the corresponding st…

Pyruvate decarboxylationPyruvate dehydrogenase kinaseEcologyPyruvate Dehydrogenase ComplexPyruvate dehydrogenase phosphataseBiologyPyruvate dehydrogenase complexPhysiology and BiotechnologyApplied Microbiology and BiotechnologyPyruvate carboxylaseCulture MediaGram-Positive CocciBiochemistryPyruvate oxidase activityFermentationPyruvic AcidFermentationAnaerobiosisDihydrolipoyl transacetylaseLeuconostocFood ScienceBiotechnologyApplied and environmental microbiology
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Unravelling Radicals Reactivity Towards Carbon Nanotubes Manipulation/Functionalization

2016

Carbon Nanotubes (CNTs) chemistry is under constant evolution, as a consequence of the deep interest of the scientific community in finding new applications for these versatile materials. New and old synthetic protocols are used for improving the control of the functionalization degree of the final materials and for offering to scientists the possibility to fine-tune their final properties. In this Review, we focus the attention on radical reactions, a class of protocols characterized by small number of steps, different degrees of functionalization and enhanced solubility of the final modified CNTs, in the desired environment. The most well-known protocols are analysed providing some releva…

Radical02 engineering and technologyCarbon nanotube010402 general chemistryPhotochemistry01 natural sciencesCarbon nanotubelaw.inventioncarboxylationBirch reductionlawepoxidationOrganic chemistryReactivity (chemistry)diazonium saltsradicalBirch reductionChemistryOrganic Chemistry021001 nanoscience & nanotechnologyradicals0104 chemical sciencesCarboxylationdiazonium saltSurface modificationCarbon Nanotubespolymer grafting0210 nano-technologyCarbon Nanotubes radicals carboxylation diazonium salts Birch reduction epoxidation polymer grafting
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