Search results for " Synthesis"

showing 10 items of 1625 documents

On the Rearrangement in Dioxane/Water of (Z)-Arylhydrazones of 5-Amino-3-benzoyl-1,2,4-oxadiazole into (2-Aryl-5-phenyl-2H-1,2,3-triazol-4-yl)ureas: …

2006

We have recently evidenced an interesting differential behavior in the reactivity in dioxane/water between the (Z)-2,4-dinitrophenylhydrazone (1a) and the (Z)-phenylhydrazone (1b) of 5-amino-3-benzoyl-1,2,4- oxadiazole. The former rearranges into the relevant triazole 2a only at pS+ > 4.5 while undergoing hydrolysis at high proton concentration (pS+ < 3.5); on the contrary, the latter rearranges into 2b in the whole pS+ range examined (0.1 e pS+ e 14.9). Thus, for a deeper understanding of these differences we have now collected kinetic data on the rearrangement in dioxane/water of a series of 3- or 4-substituted (Z)-phenylhydrazones (1c-l) of 5-amino-3-benzoyl-1,2,4-oxadiazole in a wide ra…

OxadiazolesMolecular StructureStereochemistryArylOrganic ChemistryHydrazonesTriazoleSubstituentWaterOxadiazolemononuclear rearrangement of heterocycles acid catalysis base catalysisTriazolesChemical synthesisMedicinal chemistryCatalysisDioxanesKineticschemistry.chemical_compoundAcid catalysischemistryThermodynamicsAmine gas treatingReactivity (chemistry)
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Stereoselective synthesis and application of tridentate aminodiols derived from (+)-pulegone

2016

Abstract A library of tridentate aminodiols, derived from naturally occurring (R)-(+)-pulegone, was synthesized and applied as chiral catalysts in the addition of diethylzinc to benzaldehyde. The reduction of pulegone furnished pulegol, which was transformed into allylic trichloroacetamide via Overman rearrangement of the corresponding trichloroacetimidate. The protected enamine was subjected to dihydroxylation with OsO4/NMO system resulting in a 1:1 mixture of (1R,2R,4R)- and (1S,2S,4R)-aminodiol diastereomers. After the removal of the trichloroacetyl protecting groups, the obtained primary aminodiols were transformed into secondary ones. The regioselectivity of the ring closure of the N-b…

OxazolidineAllylic rearrangement010405 organic chemistryOrganic ChemistryRegioselectivityDiethylzinc010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesEnamineOverman rearrangementInorganic ChemistryBenzaldehydechemistry.chemical_compoundchemistryDihydroxylationOrganic chemistryPhysical and Theoretical Chemistryta116stereoselective synthesistridentate aminodiolsTetrahedron : Asymmetry
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Organocatalytic enantioselective synthesis of 2,5,5-trisubstituted piperidines bearing a quaternary stereocenter. Vinyl sulfonamide as a new amine pr…

2020

An organocatalytic desymmetrizing intramolecular aza-Michael reaction with vinyl sulfonamides as nucleophilic nitrogen source has been devised for the synthesis of a new family of 2,5,5-trisubstituted piperidines bearing a quaternary sterocenter. The process takes place with excellent levels of enantioselectivity and moderate to good diastereoselectivity. The vinyl sulfonamide moiety can be removed by means of an ozonolysis reaction.

OzonolysisChemistryMetals and AlloysEnantioselective synthesisGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterNucleophileIntramolecular forceMaterials ChemistryCeramics and CompositesMoietyOrganic chemistryAmine gas treatingProtecting groupChemical Communications
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Synthesis of (±)-(E)-2,6-dimethyl-6-hydroxyocta-2,7-dienoic acid and the corresponding amide (“acacialactam”)

1994

Abstract The total synthesis of the title compounds in racemic form is described. Linalool was used as the starting material and transformed into the target molecules in 6 steps. The synthetic amide displays spectral properties identical to those reported for the natural compound acacialactam, indicating that the structure proposed for the latter compound is not correct.

OzonolysisOrganic ChemistrySpectral propertiesTotal synthesisBiochemistrychemistry.chemical_compoundLinaloolchemistryAmideDrug DiscoveryWittig reactionMoleculeOrganic chemistryAliphatic compoundTetrahedron Letters
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Few-layer Black Phosphorous Catalyzes Radical Additions to Alkenes Faster than Low-valence Metals

2020

Abstract The substitution of catalytic metals by p‐block main elements has a tremendous impact not only in the fundamentals but also in the economic and ecological fingerprint of organic reactions. Here we show that few‐layer black phosphorous (FL‐BP), a recently discovered and now readily available 2D material, catalyzes different radical additions to alkenes with an initial turnover frequency (TOF0) up to two orders of magnitude higher than representative state‐of‐the‐art metal complex catalysts at room temperature. The corresponding electron‐rich BP intercalation compound (BPIC) KP6 shows a nearly twice TOF0 increase with respect to FL‐BP. This increase in catalytic activity respect to t…

P-block catalysisIronIntercalation (chemistry)Inorganic chemistryAlkenes010402 general chemistryblack phosphorus01 natural sciencesCatalysisCatalysislaw.inventionInorganic ChemistryMetalchemistry.chemical_compoundironCatàlisilawPhysical and Theoretical ChemistryMaterialsradical additionValence (chemistry)Full Paperalkenes010405 organic chemistryGraphenep-block catalysisOrganic ChemistryBlack phosphorusFull Papers2D materials0104 chemical sciencesRadical additionchemistryOrganic reactionvisual_artddc:540visual_art.visual_art_mediumOrganic synthesisCarbon monoxideCHEMCATCHEM
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On the nature of macroradicals formed upon radiolysis of aqueous poly(N-vinylpyrrolidone) solutions

2020

In this work we have explored the nature of macroradicals formed upon radiolysis of aqueous poly(N-vinylpyrrolidone) (PVP) solutions using pulse radiolysis, density functional theory (DFT) and literature data. On the basis of literature data on site-specific kinetics of hydrogen abstraction from simple amides and spectra corresponding to specific radical sites on the same amides we have assessed the distribution of H-atom abstraction by `OH radicals from different positions on the pyrrolidone ring and the polymer backbone. Pulse radiolysis experiments performed at different doses per pulse and different PVP concentrations demonstrate that the H-abstracting radiolysis products are not quanti…

PULSE-RADIOLYSISMaterials sciencePulse radiolysisCROSS-LINKINGNanogelsMICROGELSPOLY(ACRYLIC ACID) NANOGELSHYDROXYL RADICALSPhotochemistry01 natural sciences030218 nuclear medicine & medical imaging03 medical and health scienceschemistry.chemical_compoundDELIVERYNanogel0302 clinical medicine0103 physical sciencesMacroradicalRadiationAqueous solution010308 nuclear & particles physicsN-VinylpyrrolidonePulse (physics)ELECTRONSNETWORKSchemistryRadiolysispoly(N-vinyl pyrrolidone)Density functional theoryDensity functional theoryMacroradicalsSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePOLYMERSRADIATION-INDUCED SYNTHESIS
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SYNTHESIS OF PYRROLO[3,2-H]QUINOLINONES WITH GOOD PHOTOCHEMOTHERAPEUTIC ACTIVITY AND NO DNA DAMAGE

2010

In the search for new photochemotherapeutic agents, a series of derivatives of the ring system pyrrolo[3,2-h]quinoline--bioisosters of the angular furocoumarin angelicin--were synthesized through a four-step synthetic approach, in reasonable overall yields. Eight of the synthesized derivatives showed a remarkable phototoxicity against a panel of four human tumor cell lines and a great dose UV-A dependence, reaching IC₅₀ values at submicromolar level. The mode of cellular death photoinduced by pyrrolo[3,2-h]quinolines was evaluated through a series of flow cytometric analysis and other tests were performed to clarify their mechanism of action.

PYRROLO[32-H]QUINOLINONESStereochemistryDNA damageClinical BiochemistryPharmaceutical SciencePhosphatidylserinesBiochemistryChemical synthesischemistry.chemical_compoundCell Line TumorFurocoumarinsDrug Discovery2-H]QUINOLINONESmedicineHumansPyrrolesPhotosensitizerMolecular BiologyMembrane Potential MitochondrialPhotosensitizing AgentsPYRROLO[3; 2-H]QUINOLINONES; ANGELICIN HETEROANALOGUES; PHOTOCHEMOTHERAPY; PHOTOTOXICITYFurocoumarinOrganic ChemistryBiological activitySettore CHIM/08 - Chimica FarmaceuticaPHOTOCHEMOTHERAPYPHOTOTOXICITYPYRROLO[3ANGELICIN HETEROANALOGUESMechanism of actionchemistryQuinolinesLactamMolecular Medicinemedicine.symptomReactive Oxygen SpeciesPhototoxicityDNA Damage
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Development of conservation methods for the restoration of paper materials

Paper, one of the most common materials of Cultural Heritage, undergoes serious deterioration caused by physical, chemical and biological factors. One of the main causes of deterioration is the acidic and/or oxidative environment. The studies of deterioration and conservation of paper have been increasing and require further development of methods and treatments that can stabilize and strengthen the paper. Various conservation treatments are being applied to model and to historical paper by using different chemicals methods. Their effectiveness for conservation and restoration are under study. Internal and external factors degrade the paper by promoting various reaction pathways. The two mo…

Papernanolimetert-butyl amine borane complexnanoparticles synthesisdeacidificationPaper; deacidification; reduction; nanolime; tert-butyl amine borane complex; nanoparticles synthesisreduction
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A qualitative meta-synthesis of patients' experiences of intra- and inter-hospital transitions

2013

Aim. To aggregate, interpret and synthesize findings from qualitative studies of patients’ experiences on being transferred/in transition from one hospital to another or from one ward to another. Background. Studies about patients’ experiences of transfer focused on concepts such as transfer stress, transfer anxiety, and translocation syndrome; however, a metasynthesis on experiences of transition across different patient populations was lacking. Design. The meta-synthesis approach was based on the guidelines by Sandelowski and Barroso. Data source. Six electronic databases were searched for articles published between the years 1999-2011, based on the target phenomenon: patients’ experience…

Patient TransferMeta synthesisEvidence-based practicebusiness.industrymedia_common.quotation_subjectIntervention studiesFeelingNursingAdaptation PsychologicalHumansMedicineAnxietyQuality (business)transition metasynthesismedicine.symptomNurse-Patient RelationsbusinessAttitude to HealthQualitative ResearchStress PsychologicalGeneral NursingQuality of Health Caremedia_commonQualitative researchClinical nursingJournal of Advanced Nursing
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Oxide or carbide nanoparticles synthesized by laser ablation of a bulk Hf target in liquids and their structural, optical, and dielectric properties

2016

International audience; Laser ablation of a bulk Hf target in deionized (DI) water, ethanol, or toluene was carried out for the production of nanoparticles' colloidal solutions. Due to the interaction of the ablation plasma plume species with the species which are produced by the liquid decomposition at the plume-liquid interface, hafnia (HfO2) nanoparticles are synthesized in DI water, hafnium carbide (HfC) nanoparticles in toluene, and a mixture of these in ethanol. The hafnia nanoparticles are in the monoclinic low temperature phase and in the tetragonal and fcc high temperature phases. Their size distribution follows log-normal function with a median diameter in the range of 4.3–5.3 nm.…

PermittivityMaterials scienceThin filmsInorganic chemistryAnalytical chemistryGeneral Physics and AstronomyNanoparticlePlasma sources02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyLaser ablation synthesis in solutionNanocompositesPulsed laser depositionCarbideAbsorption spectroscopy[CHIM]Chemical SciencesThin filmLaser ablationbiologyCrystal structure[SPI.MECA]Engineering Sciences [physics]/Mechanics [physics.med-ph]021001 nanoscience & nanotechnologyHafniabiology.organism_classificationLaser ablationX-ray diffraction0104 chemical sciencesDielectric propertiesNanoparticlesSet theory0210 nano-technologyJournal of Applied Physics
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