Search results for "Diene"

showing 10 items of 623 documents

Randomized placebo-controlled trial comparing fluticasone aqueous nasal spray in mono-therapy, fluticasone plus cetirizine, fluticasone plus monteluk…

2004

BACKGROUND: Corticosteroids are considered to be particularly effective in reducing nasal congestion and are therefore recommended as first-line treatment in allergic rhinitis patients with moderate to severe and/or persistent symptoms. OBJECTIVE: We compared the clinical efficacy of fluticasone propionate aqueous nasal spray (FPANS) 200 microg given once daily, administered in mono-therapy or combined therapy with a H1 receptor antagonist (cetirizine, CTZ) or with a leukotriene antagonist (montelukast, MSK), and the combined therapy of CTZ plus MSK in the treatment of patients affected by allergic rhinitis to Parietaria during natural pollen exposure. In addition, we examined the effect of…

CyclopropanesMaleAllergySettore MED/09 - Medicina Internamedicine.medical_treatmentseasonal allergic rhinitisAcetatesGastroenterologyImmunology and AllergyMedicineChildFluticasonepollen seasonRandomized placebo-controlled trialBlood Proteinsrespiratory systemEosinophil Granule ProteinsMiddle AgedCetirizineAnesthesiamontelukastHistamine H1 AntagonistsQuinolineseosinophil cationic proteinDrug Therapy CombinationFemaleeosinophilsmedicine.symptommedicine.drugAdultmedicine.medical_specialtyAdolescentImmunologyNasal congestionSulfidesPlaceboFluticasone propionateDrug Administration ScheduleRibonucleasesDouble-Blind MethodInternal medicineHumansRandomized placebo-controlled trial; fluticasone; cetirizine; montelukast; seasonal allergic rhinitisGlucocorticoidsMontelukastAdministration IntranasalAnalysis of Variancerhinorrheafluticasone propionatebusiness.industrynasal lavageRhinitis Allergic Seasonalmedicine.diseaseCetirizineAndrostadienesParietariaNasal sprayFluticasoneLeukotriene AntagonistsNasal administrationbusinessClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
researchProduct

Darba drošības indeksācijas pilnveidošana kā preventīvo pasākumu efektivitātes paaugstināšanas faktors Valsts ugunsdzēsības un glābšanas dienesta Rīg…

2020

“Darba drošības indeksācijas pilnveidošana kā preventīvo pasākumu efektivitātes paaugstināšanas faktors valsts ugunsdzēsības un glābšanas dienesta Rīgas reģiona pārvaldē”. Darba autors: Andis Prūsis. Darba zinātniskais vadītājs: Valsts ugunsdzēsības un glābšanas dienesta Civilās aizsardzības pārvaldes Resursu pārvaldīšanas nodaļas vecākais inspektors, Mg. darba aizsardzībā Uldis Ķevers. Darba izklāsts uz 85 lapām, ietver 10 attēlus, 48 tabulas, 23 pielikumus un 23 informatīvos avotus. Pētījums sastāv no 4 daļām. Pirmajā daļā ir apkopota un analizēta informācija par darba aizsardzības likumdošanu Eiropā un Latvijā, Valsts ugunsdzēsības un glābšanas dienesta struktūru, sastopamajiem darba vid…

Darba vides riskiRisku novērtēšanaValsts ugunsdzēsības un glābšanas dienestsDarba vides aizsardzība un ekspertīzeObligātās veselības pārbaudes
researchProduct

The molecular dynamics of thermoreversible networks as studied by broadband dielectric spectroscopy

1995

Polybutadienes modified by a small number of 4-phenyl-1,2,4-triazoline-3,5-dione form thermoreversible networks via hydrogen bonding between the polar stickers. The molecular dynamics of systems with different contents of polar stickers are investigated by broadband dielectric spectroscopy in the frequency regime of 10−1–109 Hz. Unmodified polybutadiene shows two relaxation processes, the α-relaxation which is correlated to the dynamic glass transition of the polybutadiene, and a β-relaxation corresponding to a local relaxation of polybutadiene segments. In the polar functionalized systems, besides these two relaxations, an additional relaxation process (called α*) is observed, which occurs…

Dielectric absorptionPolymers and PlasticsChemistryDissociation (chemistry)Dielectric spectroscopyReptationMolecular dynamicsDipoleColloid and Surface ChemistryPolybutadieneChemical physicsPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryGlass transitionColloid & Polymer Science
researchProduct

The catalytic effects of a thiazolium salt in the oxa-Diels–Alder reaction between benzaldehyde and Danishefsky's diene: a molecular electron density…

2021

The oxa-Diels–Alder (ODA) reaction of benzaldehyde with Danishefsky's diene in the presence of a [thiazolium][Cl] salt, as a model of an ionic liquid, has been studied within Molecular Electron Density Theory (MEDT) at the M06-2X/6-311G(d,p) computational level. The formation of two hydrogen bonds (HBs) between the thiazolium cation and the carbonyl oxygen of benzaldehyde modifies neither the electrophilic character of benzaldehyde nor its electronic structure substantially but accelerates the reaction considerably. This ODA reaction presents an activation energy of 4.5 kcal mol−1; the formation of the only observed dihydropyranone is strongly exothermic by −28.8 kcal mol−1. The presence of…

Diene010405 organic chemistryHydrogen bondOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesCatalysisBenzaldehydechemistry.chemical_compoundchemistryElectrophilePhysical and Theoretical ChemistryDanishefsky's dieneDiels–Alder reactionOrganic & Biomolecular Chemistry
researchProduct

New reactions and step economy: the total synthesis of (±)-salsolene oxide based on the type II transition metal-catalyzed intramolecular [4+4] cyclo…

2006

Studies on the viability of the type II nickel-catalyzed intramolecular [4+4] cycloaddition of bis-dienes show that it is influenced by both diene substitution and geometry. Both E- and Z-isomers of 19 and 20 react, albeit at markedly different rates, to afford cycloadducts, whereas only the Z-isomer of 9 (and not the E-isomer) reacts to give 8 and 25. Chemoselective elaboration of 8 to (±)-salsolene oxide (7) was used to confirm the cycloadduct structure while establishing a step economical route to the natural product.

DieneChemistryOrganic ChemistryOxideTotal synthesisBiochemistryMedicinal chemistryCycloadditionCatalysischemistry.chemical_compoundTransition metalIntramolecular forceDrug DiscoveryOrganic chemistryTetrahedron
researchProduct

Understanding the participation of 3-nitropyridine in polar Diels–Alder reactions. A DFT study

2015

The reactivity of 3-nitropyridine acting as an electrophilic dienophile in polar Diels-Alder (P-DA) reactions toward three different dienes of increased nucleophilicity has been theoretically studied using DFT methods at the MPWB1K/6-31G(d) level. It has been observed that this aromatic heterocyclic system suffers cycloaddition reactions yielding isoquinoline derivatives. The present DFT study establishes that while the P-DA reactions with isoprene and 1-methoxy-1,3-butadiene take place through a two-stage one-step mechanism, the use of the strong nucleophilic Danishefsky's diene changes the mechanism to a two-step one with formation of a zwitterionic intermediate. These P-DA reactions are …

DieneChemistryPARR FUNCTIONSCiencias QuímicasRegioselectivityREGIOSELECTIVITYCondensed Matter PhysicsBiochemistryCycloaddition3-NITROPYRIDINEchemistry.chemical_compoundQuímica OrgánicaNucleophileMOLECULAR MECHANISMSComputational chemistryDFT INDICESElectrophileOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryIsoquinolinePOLAR DIELS-ALDERCIENCIAS NATURALES Y EXACTASIsopreneComputational and Theoretical Chemistry
researchProduct

Mechanistic details of the domino reaction of nitronaphthalenes with the electron-rich dienes. A DFT study

2008

Abstract The reaction of 1-nitronaphthalene ( 1 ) with the Danishefsky diene ( 2 ) to give the dihydrophenanthrene derivative 11 has been theoretically studied using DFT methods. This reaction is a domino process that is initialized by a polar Diels–Alder reaction between 1 and 2 to give the formally [2 + 4] cycloadduct 3 . The subsequent concerted elimination of nitrous acid ( 4 ) from 3 yields 11 . Analysis of the global reactivity indices as well as the thermodynamic data for this domino process indicate that while the large electrophilic character of 1 together with the large nucleophilic character of 2 are responsible for the participation of these reagents in a polar Diels–Alder react…

DieneCondensed Matter PhysicsPhotochemistryBiochemistrychemistry.chemical_compoundElimination reactionNucleophilechemistryCascade reactionComputational chemistryReagentElectrophileReactivity (chemistry)Physical and Theoretical ChemistryDerivative (chemistry)Journal of Molecular Structure: THEOCHEM
researchProduct

Selective, homogeneous hydrogenation of cycloheptatriene to cycloheptene catalyzed by (η4-cycloocta-1,5-diene)(η6-cyclohepta-1,3,5-triene)ruthenium(0)

1980

Abstract In the presence of small amounts of [Ru(η 4 -COD)](η 6 -C 8 H 10 )] (1), cycloheptatriene is hydrogenated to cycloheptene, under one atmosphere of hydrogen at room temperature in homogeneous phase. The formation of a small amount of cyclooctene and the existence of an induction period, which do not occur when [Ru(η 4 -COD)(η 6 -C 7 H 8 )] (2) is used as the catalyst, suggest that 2 is the real catalyst. The selectivity of this hydrogenation is 100% in n-hexane as solvent, 99.5% in THF, and low in ethanol. Conversion is quantitative in THF and ethanol, but not more than 65% in n-hexane. In the presence of 1 or 2, cycloheptene is rapidly hydrogenated to cycloheptane in THF and ethano…

DieneInduction periodOrganic Chemistrychemistry.chemical_elementCycloheptatrienePhotochemistryBiochemistryMedicinal chemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryCycloocteneMaterials ChemistryCycloheptenePhysical and Theoretical ChemistryCycloheptaneJournal of Organometallic Chemistry
researchProduct

Selective homogeneous hydrogenation of cycloocta-1,5, and cycloocta-1,3-diene to cyclooctene in the presence of (η4-cycloocta-1,5-diene)(η6-cycloocta…

1983

Cyclooctadiene isomers (1,3- and 1,5-COD) are selectively, homogenously hydrogenated to cyclooctene (C8H14) in tetrahydrofuran (THF) solution, under mild conditions of temperature (20 °C) and hydrogen pressure (1 atm), in the presence of catalytic amounts of (cycloocta-1,5-diene)(cycloocta-1,3,5,-triene)ruthenium(0), [Ru(η4-COD)(η6-C8H10)] (1). The rate of hydrogenation is higher when 1,3-COD is the substrate. Evidence for the isomerization 1,5-COD → 1,3-COD is reported. Similar studies carried out in several alcoholic solutions, although showing a decreased selectivity in the hydrogenation, confirm the isomerization 1,5-COD → 1,3-COD, and allow a discrimination between the isomerization an…

DieneNorbornadienechemistry.chemical_elementNoyori asymmetric hydrogenationPhotochemistryMedicinal chemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryCycloocteneMaterials ChemistryPhysical and Theoretical ChemistryIsomerizationCyclooctadieneInorganica Chimica Acta
researchProduct

Polar Diels–Alder reactions using electrophilic nitrobenzothiophenes. A combined experimental and DFT study

2015

Abstract The reactions between 2- and 3-nitrobenzothiophenes with three dienes of different nucleophilicity, 1-methoxy-3-trimethylsilyloxy-1,3-butadiene, 1-trimethylsilyloxy-1,3-butadiene and isoprene developed in anhydrous benzene and alternative under microwave irradiation with molecular solvents or in free solvent conditions, respectively, for produce dibenzothiophenes permit to conclude that both nitroheterocycles act as electrophile with the cited dienes. In the cases of the dienes 1-methoxy-3-trimethylsilyloxy-1,3-butadiene and 1-trimethylsilyloxy-1,3-butadiene which posses major nucleophilicity the observed product is the normal cycloaddition one. However when the diene is isoprene t…

DieneOrganic ChemistryCycloadditionAnalytical ChemistryInorganic ChemistrySolventchemistry.chemical_compoundchemistryNucleophileDibenzothiopheneElectrophileOrganic chemistryBenzeneSpectroscopyIsopreneJournal of Molecular Structure
researchProduct