Search results for "enones"

showing 10 items of 61 documents

Addition of Nucleophiles to Fluorinated Michael Acceptors

2016

A series of nucleophiles, including primary and secondary amines, primary alcohols, and thiols, as well as diethyl malonate and nitromethane, were added to different fluorinated Michael acceptors including 2-fluoroalk-1-en-3-ones and 2-fluoro-1-phenylprop-2-en-1-one. The resulting beta-substituted afluoro ketones were isolated in 34-92 % yield, depending on the substrate and the nucleophile. The best yields were obtained with secondary amines and with p-methylthiophenol.

Nucleophilic additionPrimary (chemistry)Nitromethane010405 organic chemistryOrganic Chemistrychemistry.chemical_elementEnonesFluorine010402 general chemistry01 natural sciences0104 chemical sciencesDiethyl malonatechemistry.chemical_compoundchemistryNucleophileYield (chemistry)Michael additionFluorineMichael reactionOrganic chemistryPhysical and Theoretical ChemistryNucleophilic addition
researchProduct

PPAR-γ Agonist GW1929 But Not Antagonist GW9662 Reduces TBBPA-Induced Neurotoxicity in Primary Neocortical Cells

2013

Tetrabromobisphenol A (2,2-bis(4-hydroxy-3,5-dibromophenyl)propane; TBBPA) is a widely used brominated flame retardant. TBBPA induces neuronal damage, but the mechanism by which this occurs is largely unknown. We studied the possible involvement of peroxisome proliferator-activated receptor gamma (PPAR-γ) in TBBPA-induced apoptosis and toxicity in mouse primary neuronal cell cultures. TBBPA enhanced both, caspase-3 activity and lactate dehydrogenase (LDH) release in neocortical cells after 6 and 24 h of exposition. These data were supported at the cellular level with Hoechst 33342 staining. Immunoblot analyses showed that, compared with control cells, 10 μM TBBPA decreased the expression of…

PPAR-γTime FactorsNeuroscience(all)Polybrominated BiphenylsPeroxisome proliferator-activated receptorGW1929Caspase 3ApoptosisNeocortexPharmacologyBiologyToxicologyNeuroprotectionBenzophenonesMicemedicineNeurotoxicityAnimalsAnilidesReceptorCells Culturedchemistry.chemical_classificationNeuronsDose-Response Relationship DrugL-Lactate DehydrogenaseCaspase 3General NeuroscienceNeurotoxicityApoptotic bodymedicine.diseasePPAR gammaTBBPANeuroprotective AgentschemistryCell cultureApoptosisTyrosineNeurotoxicity SyndromesOriginal ArticleCentral Nervous System AgentsNeurotoxicity Research
researchProduct

Development of predictive retention-activity models of butyrophenones by biopartitioning micellar chromatography

2001

The predictive and interpretative capability of quantitative chromatographic retention-biological activity models is supported by the fact that in adequate experimental conditions the solute partitioning into the chromatographic system can emulate the solute partitioning into lipid bilayers of biological membranes, which is the basis of drug and metabolite uptake, passive transport across membranes and bioaccumulation. The use of retention data obtained in biopartitioning micellar chromatography (BMC) has been demonstrated to be helpful in describing the biological behaviour of different kinds of drugs. In this chromatographic system, polioxyethylene 23 lauryl ether Brij35 micellar mobile p…

PharmacologyNeuroleptic DrugsChromatographyPassive transportChemistryMetaboliteClinical BiochemistryBiological membraneGeneral MedicineBiochemistryMicelleAnalytical Chemistrychemistry.chemical_compoundMembraneStationary phaseDrug DiscoveryButyrophenonesMolecular BiologyBiomedical Chromatography
researchProduct

Intramolecular Interactions in the Triplet Excited States of Benzophenone–Thymine Dyads

2005

Time-resolved and product studies on the synthesized dyads 1 and 2 have provided evidence that the benzophenone-to-thymine orientation strongly influences intramolecular photophysical and photochemical processes. The prevailing reaction mechanism has been established as a Paterno-Büchi cycloaddition to give oxetanes 3-6; however, the ability of benzophenone to achieve a formal hydrogen abstraction from the methyl group of thymidine has also been evidenced by the formation of photoproducts 7 and 8. These processes have been observed only in the case of the cisoid dyad 1. Adiabatic photochemical cycloreversion of the oxetane ring is achieved upon direct photolysis to give the starting dyad 1 …

PhotochemistryOrganic ChemistryGeneral ChemistryOxetaneHydrogen atom abstractionPhotochemistryCatalysisCycloadditionBenzophenoneschemistry.chemical_compoundchemistryEthers CyclicExcited stateIntramolecular forceBenzophenoneTriplet stateThymineThymidineMethyl groupChemistry - A European Journal
researchProduct

Resolving the Benzophenone DNA-Photosensitization Mechanism at QM/MM Level

2015

International audience; Benzophenone, the parent of the diarylketone family, is a versatile compound commonly used as a UV blocker. It may also trigger triplet-based DNA photosensitization. Therefore, benzophenone is involved in DNA photodamage induction. In the absence of experimentally resolved structure, the mechanism of DNA damage production remains elusive. Employing a hybrid quantum mechanics/molecular mechanics approach, here we address the spin transfer mechanism between this drug and proximal thymine, that is, the DNA nucleobase most prone to suffer triplet damages.

Photosensitizing AgentsDNA PhotosensitizationDNA damageChemistryDNAMolecular Dynamics SimulationPhotochemistryMolecular mechanicsQM/MM3. Good healthThymineNucleobaseQM/MM[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryBenzophenoneschemistry.chemical_compoundMolecular dynamicsBenzophenoneEnergy TransferBenzophenoneQuantum TheoryGeneral Materials SciencePhysical and Theoretical ChemistryDNA
researchProduct

Protective effect of apocynin in a mouse model of chemically-induced colitis.

2013

Apocynin, a constituent of Picrorhiza kurroa, successfully inhibits NADPH oxidase and shows promise as an anti-inflammatory drug. Now, we report anti-inflammatory effects of apocynin in an experimental colitis model induced by dextran sulfate sodium as well as the effects on the mediators involved in this process. Apocynin reduced the colitis induced in mice by administration of 5 % dextran sulfate sodium during 7 days. Mice were fed a control diet or a diet supplemented with 2 % of apocynin or 2 % of rutin. Sulfasalazine (50 mg/kg, p. o.) was used as a positive control. Treatment with apocynin and rutin ameliorated the course of colonic inflammation with results similar to those of the ref…

Picrorhiza kurroaRutinAnti-Inflammatory AgentsPharmaceutical ScienceNitric Oxide Synthase Type IIPharmacologyInflammatory bowel diseaseAnalytical Chemistrychemistry.chemical_compoundRutinMiceDrug DiscoveryPicrorhizaNADPH oxidasebiologyDextran SulfateColitisBiochemistrycardiovascular systemMolecular Medicinecirculatory and respiratory physiologymedicine.druginorganic chemicalsSTAT3 Transcription FactorColonNitric OxideDinoprostoneNitric oxideSulfasalazinemedicineAnimalscardiovascular diseasesColitisPharmacologyCyclooxygenase 2 Inhibitorsbusiness.industryPlant ExtractsOrganic ChemistryTranscription Factor RelAAcetophenonesmedicine.diseaseSulfasalazineDisease Models AnimalchemistryComplementary and alternative medicineCyclooxygenase 2Apocyninbiology.proteinbusinessPhytotherapyPlanta medica
researchProduct

Generation of 6,7-Dihydro-5H-1,3,4-thiadiazolo[3,2-a]pyridines — Unexpected Products in the Reaction of 5-Ethylthio-1,3,4-thiadiazole-2-amine and 3-(…

1998

PropiophenonesChemistryOrganic ChemistryAmine gas treatingPhysical and Theoretical ChemistryMedicinal chemistryEuropean Journal of Organic Chemistry
researchProduct

Synthesis of 6,12-Disubstituted Methanodibenzo[

2019

The preparation of unprecedented 6,12-disubstituted methanodibenzo[b,f][1,5]dioxocins from pyrrolidine catalyzed self-condensation of 2′-hydroxyacetophenones is herein described. This method provides easy access to this highly bridged complex core, resulting in construction of two C–O and two C–C bonds, a methylene bridge and two quaternary centers in a single step. The intricate methanodibenzo[b,f][1,5]dioxocin compounds were obtained in up to moderate yields after optimization of the reaction conditions concerning solvent, reaction times and the use of additives. Several halide substituted methanodibenzo[b,f][1,5]dioxocins could be prepared from correspondent 2′-hydroxyacetophenones.

Pyrrolidinesself-condensationMolecular StructureenamineAcetophenonesStereoisomerism15-dioxocin2′-hydroxyacetophenoneCatalysisArticleMolecules (Basel, Switzerland)
researchProduct

Efficient flow injection and sequential injection methods for spectrophotometric determination of oxybenzone in sunscreens based on reaction with Ni(…

2001

Spectrophotometric determination of a widely used UV-filter, such as oxybenzone, is proposed. The method is based on the complexation reaction between oxybenzone and Ni(II) in ammoniacal medium. The stoichiometry of the reaction, established by the Job method, was 1:1. Reaction conditions were studied and the experimental parameters were optimized, for both flow injection (FI) and sequential injection (SI) determinations, with comparative purposes. Sunscreen formulations containing oxybenzone were analyzed by the proposed methods and results compared with those obtained by HPLC. Data show that both FI and SI procedures provide accurate and precise results. The ruggedness, sensitivity and LO…

Reaction conditionsChromatographymedicine.diagnostic_testColor reactionAnalytical chemistryBiochemistryHigh-performance liquid chromatographySensitivity and Specificitychemistry.chemical_compoundSequential injectionBenzophenoneschemistryAmmoniaNickelSpectrophotometrySpectrophotometrymedicineIndicators and ReagentsOxybenzoneQuantitative analysis (chemistry)Sunscreening AgentsStoichiometryChromatography High Pressure LiquidFresenius' journal of analytical chemistry
researchProduct

La Bibliothèque de l'abbaye de Senones des origines à la Révolution

1994

International audience

Senones[ SHS.HIST ] Humanities and Social Sciences/History[SHS.HIST] Humanities and Social Sciences/Historyabbaye[SHS.HIST]Humanities and Social Sciences/HistoryComputingMilieux_MISCELLANEOUSVosgesbibliothèque
researchProduct