Search results for "LOAD"

showing 10 items of 1967 documents

Effect of endodontic treatment on fatigue resistance of fiber posts bonding

2003

Objectives: The aim of this study is to evaluate the effect of the endodontic treatment on the fatigue resistance of endodontic post adhesive interfaces. Materials and methods: 50 single-rooted human teeth have been severed at the cement-enamel junction and randomly assigned to 5 groups receiving different endodontic treatments as follows: 1) distilled water + gutta-percha (control); 2) NaOCl 5% + gutta-percha and Pulp Canal Sealer EWT (Kerr); 3) NaOCl 5% + gutta-percha and Top Seal (Dentsply-Maillefer); 4) NaOCl 5% and EDTA 10% (alternatively) + gutta-percha and Pulp Canal Sealer EWT; 5) NaOCl 5% and EDTA 10% (alternatively) + gutta-percha and Top Seal. Subsequently, Light-Post DT #2 quart…

Cyclic loading fiber post bonding
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Incremental Delamination Processes under Cyclic Loading

2012

Cyclic loadinigSettore ICAR/08 - Scienza Delle Costruzionidelamination
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Variational methods for the steady state response of elastic–plastic solids subjected to cyclic loads

2003

Abstract Solids (or structures) of elastic–plastic internal variable material models and subjected to cyclic loads are considered. A minimum net resistant power theorem, direct consequence of the classical maximum intrinsic dissipation theorem of plasticity theory, is envisioned which describes the material behavior by determining the plastic flow mechanism (if any) corresponding to a given stress/hardening state. A maximum principle is provided which characterizes the optimal initial stress/hardening state of a cyclically loaded structure as the one such that the plastic strain and kinematic internal variable increments produced over a cycle are kinematically admissible. A steady cycle min…

Cyclic stressApplied MathematicsMechanical EngineeringRatchetMathematical analysisPlasticityDissipationCondensed Matter PhysicsShakedownMaximum principleMechanics of MaterialsModeling and SimulationHardening (metallurgy)Limit loadGeneral Materials ScienceMathematicsInternational Journal of Solids and Structures
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1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity, through 1,3-Dipolar Cycloadditions

2014

1,3-Dipolar cycloaddition reactions can be considered a powerful synthetic tool in the building of heterocyclic rings, with applications in different fields. In this review we focus on the synthesis of biologically active compounds possessing the 1,2,3-triazole core through 1,3-dipolar cycloaddition reactions. The 1,2,3-triazole skeleton can be present as a single disubstituted ring, as a linker between two molecules, or embedded in a polyheterocycle. The cycloaddition reactions are usually catalysed by copper or ruthenium. Domino reactions can be achieved through dipolarophile anion formation, generally followed by cyclisation. The variety of attainable heterocyclic structures gives an ill…

Cycloaddition / Nitrogen heterocycles / Domino reactions / Homogeneous catalysis / Enzyme catalysis / Biological activity / Medicinal chemistrySettore CHIM/03 - Chimica Generale E InorganicaCycloaddition Nitrogen heterocycles Domino reactions Homogeneous catalysis Enzyme catalysis Biological activity Medicinal chemistrySettore CHIM/08 - Chimica Farmaceutica
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Metal-Free Diastereo- and Enantioselective Dearomative Formal [3 + 2] Cycloaddition of 2-Nitrobenzofurans and Isocyanoacetate Esters

2022

The diastereo- and enantioselective dearomative formal [3 + 2] cycloaddition of 2-nitrobenzofurans and α-aryl-α-isocyanoacetate esters provides tricyclic compounds bearing the 3a,8b-dihydro-1H-benzofuro[2,3-c]pyrrole framework with three consecutive stereogenic centers. The reaction was enabled by a cupreine-ether organocatalyst. The reaction products were obtained with almost full diastereoselectivity and with excellent enantiomeric excesses for a number of substituted 2-nitrobenzofurans and isocyanoacetates.

Cycloaddition ReactionCatàlisiCompostos orgànicsOrganic ChemistryEstersStereoisomerismPhysical and Theoretical ChemistryBiochemistryCatalysisBenzofuransReaccions químiques
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Gold(I)-Catalyzed Intermolecular Cycloaddition of Allenamides with α,β-Unsaturated Hydrazones: Efficient Access to Highly Substituted Cyclobutanes

2014

α,β-Unsaturated N,N-dialkyl hydrazones undergo a mild [2 + 2] cycloaddition to allenamides when treated with a suitable gold catalyst. The method, which represents the first application of N,N-dialkyl hydrazones in gold catalysis, is compatible with a wide variety of substituents at the alkenyl moiety of the hydrazone component, proceeds with excellent levels of regio- and diastereoselectivity, and provides densely substituted cyclobutanes with good to excellent yields.

CyclobutanesLetterHydrazoneStereoisomerismBiochemistryMedicinal chemistryCatalysisCatalysisCombinatorial Chemistry TechniquesMoleculeOrganic chemistryMoietyPhysical and Theoretical ChemistryCycloadditionchemistry.chemical_classificationCycloaddition ReactionMolecular StructureOrganic ChemistryIntermolecular forceHydrazonesStereoisomerismAllenamidesCycloaddition3. Good healthAlkadienes:Investigación::23 Química [Materias]chemistryGoldCyclobutanes
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The domino reaction between 4,6-dinitrobenzofuroxan and cyclopentadiene. Insights on the nature of the molecular mechanism

2004

Abstract The molecular mechanism of the domino reaction between 4,6-dinitrobenzofuroxan, 1 , and cyclopentadiene, Cp, to give the adduct 11 is examined through density functional theory (DFT) calculations at B3LYP/6-31G* level. This domino reaction comprises two consecutive formally [4+2] cycloadditions. The first one is a two-center addition initialized by the nucleophilic attack of Cp to the more electrophilic center of 1 . The subsequent cyclization can take place along two competitive channels associated to the formation of a second C–C bond yielding the formally [2+4] cycloadduct 9 , or a C–O bond yielding the formally [4+2] cycloadduct 10 . The second cycloaddition is a stepwise proce…

CyclopentadieneChemistryCondensed Matter PhysicsBiochemistryPolarizable continuum modelDominoCycloadditionchemistry.chemical_compoundCascade reactionNucleophileComputational chemistryReactivity (chemistry)Physical and Theoretical ChemistrySolvent effectsJournal of Molecular Structure: THEOCHEM
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A PM3 study of the molecular mechanism for the cycloaddition between cyclopentadiene and protonated pyridine-imine derivatives

2001

Abstract The molecular mechanism of the cycloaddition reaction between cyclopentadiene (CP) and three pyridine-imine derivatives has been studied by means of PM3 semiempirical method. The role of the protonation, endo/exo and π-facial stereoselectivity are analyzed and discussed. In neutral conditions the cycloaddition between CP and the pyridine-imine takes place along a concerted mechanism. Protonation on both nitrogen atoms brings out that the reaction pathway takes with a very low barrier along a stepwise mechanism. PM3 results are capable to find the key factors governing this chemical reaction and to explain the experimental outcome.

CyclopentadieneConcerted reactionImineProtonationCondensed Matter PhysicsPhotochemistryBiochemistryChemical reactionCycloadditionchemistry.chemical_compoundchemistryComputational chemistryPyridineStereoselectivityPhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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Real-world experience with the all-oral, interferon-free regimen of ombitasvir/paritaprevir/ritonavir and dasabuvir for the treatment of chronic hepa…

2017

Summary Real-world studies are relevant to complement clinical trials on novel antiviral therapies against chronic hepatitis C; however, clinical practice data are currently limited. This study investigated effectiveness and safety of ombitasvir/paritaprevir/ritonavir (OBV/PTV/r)±dasabuvir (DSV)±ribavirin (RBV) for treatment of HCV genotype (GT) 1 and GT4 infection in a large real-world cohort. The German Hepatitis C Registry is an observational cohort study prospectively collecting clinical practice data on direct-acting antiviral therapies. Patients with GT1/4 infection treated with OBV/PTV/r±DSV±RBV were analysed. Effectiveness was assessed by sustained virologic response in 558 patients…

CyclopropanesLiver CirrhosisMaleHepacivirusSeverity of Illness IndexCohort Studieschemistry.chemical_compound0302 clinical medicine2-NaphthylamineGermanyMedicineAnilides030212 general & internal medicineSulfonamidesDasabuvirValineHepatitis CMiddle AgedViral LoadInfectious DiseasesTreatment Outcome030211 gastroenterology & hepatologyDrug Therapy CombinationFemalemedicine.drugAdultmedicine.medical_specialtyMacrocyclic CompoundsGenotypeProlineLactams Macrocyclic03 medical and health sciencesVirologyOmbitasvir/paritaprevir/ritonavirInternal medicineHumansUracilAgedRitonavirHepatologybusiness.industryHepatitis C Chronicmedicine.diseaseVirologyOmbitasvirDiscontinuationRegimenchemistryParitaprevirRitonavirCarbamatesbusinessJournal of viral hepatitis
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Real-world effectiveness of ombitasvir/paritaprevir/ritonavir±dasabuvir±ribavirin in patients with hepatitis C virus genotype 1 or 4 infection: A met…

2017

The direct-acting antiviral regimen of ombitasvir (OBV)/paritaprevir (PTV)/ritonavir (r) ± dasabuvir (DSV) ± ribavirin (RBV) demonstrated high rates of sustained viral response at post-treatment week 12 (SVR12) in clinical trials for treatment of hepatitis C virus (HCV) genotypes (GT) 1 and 4. To confirm the effectiveness of this regimen in the real world, we conducted meta-analyses of published literature on 30 April 2016. Freeman-Tukey transformation determined the SVR rate within GTs 1a, 1b, and 4, as well as specific SVR rates by cirrhosis or prior treatment experience status. Rates of virologic relapse, hepatic decompensation, drug discontinuation, and serious adverse events were also …

CyclopropanesLiver CirrhosisSustained Virologic ResponseHCV genotypes 1 and 4ComorbidityHepacivirusmedicine.disease_causeGastroenterologymeta-analysichemistry.chemical_compound0302 clinical medicineAnilides030212 general & internal medicineSulfonamidesDasabuvirValineHepatitis CViral LoadHepatitis Creal-world effectiveneInfectious DiseasesTreatment Outcome2D; 3D; HCV genotypes 1 and 4; hepatitis C; meta-analysis; real-world effectiveness; Hepatology; Infectious Diseases; Virology030211 gastroenterology & hepatologyDrug Therapy Combinationmedicine.drug3Dmedicine.medical_specialtyMacrocyclic CompoundsGenotypeProlineHepatitis C virusLactams MacrocyclicInfectious DiseaseAntiviral Agents03 medical and health sciencesInternal medicineVirologyRibavirinmedicineHumans2DRitonavirHepatologybusiness.industryRibavirinmedicine.diseaseOmbitasvirRegimenchemistryParitaprevirImmunologyRitonavirCarbamatesbusinessJournal of viral hepatitis
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