Search results for "acids"

showing 10 items of 3520 documents

NonclassicalPschorr andSandmeyer Reactions in Pyrazole Series

2005

The diazonium salt derived from 4-amino-N,1,3-trimethyl-N-(3-methyl-1-phenyl-1H-pyrazol-5-yl)-1H-pyrazole-5-carboxamide (14) was reacted with a mixture of CuSO4 and NaCl, with ascorbic acid as an initiator to afford the planar derivative 4,6-dihydro-1,4,6,8-tetramethyl-3-phenyldipyrazolo[3,4-b:4′,3′-d]pyridin-5(3H)-one (16) and its unexpected isomer 4,6-dihydro-3,4,6,8-tetramethyl-1-phenyldipyrazolo[4,3-b:4′,3′-d]pyridin-5(1H)-one (17), as well as the epimers (3S,4S)- (or (3S,4R)-) and (3S,4R)- (or (3S,4S)-) 4-chloro-2,4-dihydro-1′,3′,5,5′-tetramethyl-2-phenylspiro[pyrazole-3,4′(1′H)-pyrrolo[3,4-c]pyrazol]-6′(5′H)-one (18a and b, respectively). Epimers 18a and b were converted under basic c…

chemistry.chemical_classificationStereochemistryOrganic ChemistryIntercalation (chemistry)Pyrazole series Carboxylic acids Copper compounds DNA Isomers Mixtures Salts Sodium chlorideSalt (chemistry)PyrazoleAscorbic acidLinear dichroismBiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryDrug DiscoverySandmeyer reactionEpimerPhysical and Theoretical ChemistryDerivative (chemistry)Helvetica Chimica Acta
researchProduct

Stereoselective Synthesis of β-1-O-Acyl Derivatives of Carbohydrates: An Application of the Cesium Effect.

1992

Abstract The stereoselective formation of anomerically pure 1-O-acyl derivatives of protected carbohydrates is achieved by reaction of the α-glycosyl halogenoses with cesium caboxylates.

chemistry.chemical_classificationStereochemistryOrganic Chemistrychemistry.chemical_elementBiochemistryAcylationchemistry.chemical_compoundAldosechemistryCaesiumDrug DiscoverySN2 reactionOrganic chemistrylipids (amino acids peptides and proteins)StereoselectivityCarboxylateTetrahedron Letters
researchProduct

ChemInform Abstract: Glycoside Synthesis via Electrophile-Induced Activation of N-Allyl Carbamates.

2010

Abstract O-Benzyl-, O-acyl-, N-acyl- and isopropylidene-protected glycosyl N-allylcarbamates, obtained from anomerically unprotected monosaccharides and allyl isocyanate, are activated by an electrophile-induced cyclisation and react with hydroxyl compounds to form the corresponding glycosides.

chemistry.chemical_classificationStereochemistryorganic chemicalsGlycosideGeneral MedicineGlycoside synthesischemistry.chemical_compoundchemistryElectrophileMonosaccharideOrganic chemistrylipids (amino acids peptides and proteins)GlycosylAllyl isocyanateChemInform
researchProduct

Chemical characterization of traditional varietal olive oils in East of Spain

2013

Abstract The aim of this work has been to characterize the chemical composition of the eight most emblematic varietal olive oils from the West of the Mediterranean Sea. These were classified into two groups according to the International Olive Council (IOC norms): Sweet oils (Farga, Morruda and Serrana) which were compared with Arbequina as standard of the Spanish sweet oils; and bitter–spicy oils (Alfafara, Blanqueta, and Villalonga) that were compared with Picual, considered as the standard of the bitter–spicy olive oils. For the study, sampled trees were chosen in their geographically separated originating areas. They were cultivated in the traditional conditions. The variety of each sam…

chemistry.chemical_classificationStigmasterolFatty acidfood and beveragesTocopherolsBiologySterolchemistry.chemical_compoundHorticultureSterolschemistryVarietal differentiationBotanyPRODUCCION VEGETALINGENIERIA AGROFORESTALECONOMIA FINANCIERA Y CONTABILIDADFatty acidsOli d'oliva Indústria i comerçFood Science
researchProduct

Syntrophy of Crypthecodinium cohnii and immobilized Zymomonas mobilis for docosahexaenoic acid production from sucrose-containing substrates

2021

Marine heterotrophic dinoflagellate Crypthecodinium cohnii is an aerobic oleaginous microorganism that accumulates intracellular lipid with high content of 4,7,10,13,16,19-docosahexaenoic acid (DHA), a polyunsaturated ω-3 (22:6) fatty acid with multiple health benefits. C. cohnii can grow on glucose and ethanol, but not on sucrose or fructose. For conversion of sucrose-containing renewables to C. cohnii DHA, we investigated a syntrophic process, involving immobilized cells of ethanologenic bacterium Zymomonas mobilis for fermenting sucrose to ethanol. The non-respiring, NADH dehydrogenase-deficient Z. mobilis strain Zm6-ndh, with high ethanol yield both under anaerobic and aerobic condition…

chemistry.chemical_classificationSucroseZymomonasSucroseDocosahexaenoic AcidsbiologyFatty acidLevansucraseBioengineeringFructoseGeneral MedicineCrypthecodinium cohniibiology.organism_classificationApplied Microbiology and BiotechnologyZymomonas mobilischemistry.chemical_compoundchemistrySyntrophyFermentationDinoflagellidaFermentationFood scienceBiotechnologyJournal of Biotechnology
researchProduct

SN1 Reactions in Supercritical Carbon Dioxide in the Presence of Alcohols: the Role of Preferential Solvation

2016

Ethanol (3b) inhibits SN1 reactions of alkyl halides 1 in supercritical carbon dioxide (scCO2) and gives no ethers as products. The unexpected behaviour of alcohols 3 in the reaction of alkyl halides 1 with 1,3-dimethoxybenzene (2) in scCO2 under different conditions is rationalised in terms of Bronsted and Lewis acid–base equilibria of reagents, intermediates, additives and products in a singular solvent characterised by: (i) the strong quadrupole and Lewis acid character of carbon dioxide, which hinders SN2 paths by strongly solvating basic solutes; (ii) the weak Lewis base character of carbon dioxide, which prevents it from behaving as a proton sink; (iii) the compressible nature of scCO…

chemistry.chemical_classificationSupercritical carbon dioxide010405 organic chemistryOrganic ChemistryInorganic chemistrySolvation010402 general chemistryRate-determining step01 natural sciencesBiochemistry0104 chemical sciencesReaccions químiqueschemistry.chemical_compoundSN1 reactionchemistryComputational chemistryAlcoholsCarbon dioxideLewis acids and basesMetal carbon dioxide complexPhysical and Theoretical ChemistryQuímica orgànicaAlkyl
researchProduct

Regulatory activity of polyunsaturated fatty acids in T-cell signaling.

2009

n-3 Polyunsaturated fatty acids (PUFA) are considered to be authentic immunosuppressors and appear to exert beneficial effects with respect to certain immune-mediated diseases. In addition to promoting T-helper 1 (Th1) cell to T-helper 2 (Th2) cell effector T-cell differentiation, n-3 PUFA may also exert anti-inflammatory actions by inducing apoptosis in Th1 cells. With respect to mechanisms of action, effects range from the modulation of membrane receptors to gene transcription via perturbation of a number of second messenger cascades. In this review, the putative targets of anti-inflammatory n-3 PUFA, activated during early and late events of T-cell activation will be discussed. Studies h…

chemistry.chemical_classificationT-LymphocytesApoptosisCell BiologyT-Lymphocytes Helper-InducerBiologyBiochemistryArticleCell biologychemistryBiochemistrySecond messenger systemFatty Acids Unsaturatedlipids (amino acids peptides and proteins)Calcium SignalingSignal transductionProtein kinase AExtracellular Signal-Regulated MAP KinasesLipid raftProtein kinase CProtein Kinase CPolyunsaturated fatty acidDiacylglycerol kinaseCalcium signalingSignal TransductionProgress in lipid research
researchProduct

ChemInform Abstract: Microwave-Assisted Tandem Organocatalytic Peptide-Coupling Intramolecular aza-Michael Reaction: α,β-Unsaturated N-Acyl Pyrazoles…

2015

Conjugated N-acyl pyrazoles are successfully employed in the organocatalytic enantioselective intramolecular aza-Michael reaction as ester surrogates.

chemistry.chemical_classificationTandemeducationEnantioselective synthesisPeptideGeneral MedicineConjugated systembehavioral disciplines and activitiesCombinatorial chemistryhumanitiesCoupling (electronics)chemistryOrganocatalysisIntramolecular forceMichael reactionlipids (amino acids peptides and proteins)ChemInform
researchProduct

Heat capacities of butanol and pentanol in aqueous dodecyltrimethylammonium bromide solutions

1987

Heat capacities of the ternary systems water-dodecyltrimethylammonium bromide (DTAB)-butanol and water-DTAB-pentanol were measured at 25°C. The standard partial molar heat capacities of pentanol in micellar solutions show a maximum at about 0.35 mol-kg−1 DTAB that has been attributed to a micellar structural transition. This maximum tends to vanish by increasing the alcohol concentration and by decreasing the alcohol alkyl chain length; in the case of butanol it was not detected. The behavior of the standard partial molar heat capacities of alcohols in micellar solutions in the region above the cmc and below the structural transition was explained using a previously reported mass-action mod…

chemistry.chemical_classificationTernary numeral systemChemistryButanolInorganic chemistryDistribution constantBiophysicsThermodynamicsAlcoholBiochemistryMicelleHeat capacitychemistry.chemical_compoundMicellar solutionslipids (amino acids peptides and proteins)Physical and Theoretical ChemistryMolecular BiologyAlkylJournal of Solution Chemistry
researchProduct

Genetic-dependency of peroxisomal cell functions - emerging aspects

2003

This paper reviews aspects concerning the genetic regulation of the expression of the well studied peroxisomal genes including those of fatty acid beta-oxidation enzymes; acyl-CoA oxidase, multifunctional enzyme and thiolase from different tissues and species. An important statement is PPARalpha, which is now long known to be in rodents the key nuclear receptor orchestrating liver peroxisome proliferation and enhanced peroxisomal beta-oxidation, does not appear to control so strongly in man the expression of genes involved in peroxisomal fatty acid beta-oxidation related enzymes. In this respect, the present review strengthens among others the emerging concept that, in the humans, the main …

chemistry.chemical_classificationThiolaseFatty AcidsAdaptation BiologicalReceptors Cytoplasmic and NuclearPeroxisome ProliferationPeroxisome proliferator-activated receptorReviewCell BiologyPeroxisomeBiologyLipid MetabolismchemistryNuclear receptorBiochemistryPeroxisomesAnimalsHumansMolecular MedicineGeneFunction (biology)BiogenesisSignal TransductionTranscription FactorsJournal of Cellular and Molecular Medicine
researchProduct