Search results for "amine"

showing 10 items of 7299 documents

New Insight to the Chemistry of Polyaza[n]paracyclophanes. A 15N NMR Study

2001

AldehydesMagnetic Resonance SpectroscopyNitrogen IsotopesChemistryOrganic ChemistryTitrimetryHydrogen-Ion ConcentrationEthers CyclicMetalsCationsAlkanesPolyaminesOrganic chemistryChemistry (relationship)The Journal of Organic Chemistry
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Mathematical Fuzzy Logic in the Emerging Fields of Engineering, Finance, and Computer Sciences

2022

With more than 50 years of literature, fuzzy logic has gradually progressed from an emerging field to a developed research domain, incorporating the sub-domain of mathematical fuzzy logic (MFL) [...]

Algebra and Number TheorymatematiikkaLogicsyväoppiminentietojenkäsittelytieteetpääkirjoituksettekoälylaskennallinen tiederahoitusalateknologiaGeometry and Topologysoveltaminenongelmanratkaisusumea logiikkaMathematical PhysicsAnalysis
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Perusjoukon kokonaissumman estimointi Coxin regressiolla ja logistisella regressiolla : sovellus rakennusten aloitustilastoon

2012

AlipeittoLogistinen regressiomallirakentaminenregressioanalyysiHorvitz-Thompson-estimaattoritilastotCoxin regressiomalli
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H2-Antihistaminika, 15. Mitt.1) 1,n-Bis(2-imidazolyl)alkane

1983

Es wurden 1,n-Bis(2-imidazolyl)alkane mit Histamin-H2 funktionellen Seitenketten an C-4 der Imidazolringe dargestellt und auf H2-antihistaminische Aktivitat untersucht. H2-Antihistaminics, XV: 1,n-Bis(2-imidazolyl)alkanes 1,n-Bis(2-imidazolyl)alkanes with histamine H2-functional side-chains at C-4 of the imidazole rings were prepared and tested for H2-antihistaminic activity.

Alkanechemistry.chemical_classificationchemistry.chemical_compoundchemistryStereochemistryDrug DiscoveryPharmaceutical ScienceImidazoleHistamineArchiv der Pharmazie
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A Combination of Visible-Light Organophotoredox Catalysis and Asymmetric Organocatalysis for the Enantioselective Mannich Reaction of Dihydroquinoxal…

2019

[EN] An enantioselective photooxidative Mannich reaction of dihydroquinoxalinones with ketones by the merger of organophotoredox and asymmetric organocatalysis is described. This protocol features very mild reaction conditions using simple and cheap catalysts (Eosin Y and (S)-Proline) for the synthesis of chiral quinoxaline derivatives with good to high yields (up to 94%) and excellent enantioselectivities (up to 99% ee).

AlkylationActivation010402 general chemistry01 natural sciencesBiochemistryCatalysisReaccions químiqueschemistry.chemical_compoundQuinoxalineCatàlisiComplexesTertiary-AminesAcidOrganic chemistryPhysical and Theoretical ChemistryEosin YFunctionalizationMannich reactionReaction conditions010405 organic chemistryOrganic ChemistryEnantioselective synthesisMethodology0104 chemical sciencesPhotoredox catalysisEfficientchemistryOrganocatalysisFISICA APLICADAHydrogenationQuímica orgànicaVisible spectrum
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A Highly Active System for the Metal-Free Aerobic Photocyanation of Tertiary Amines with Visible Light: Application to the Synthesis of Tetraponerine…

2015

A highly efficient metal-free catalytic system for the aerobic photocyanation of tertiary amines with visible light is reported. The use of air as terminal oxidant offers an improved safety profile compared with pure oxygen, the used compact fluorescent lamp (CFL) light sources are highly economical, and no halogenated solvents are required. This system not only proves to be effective for a wide variety of trialkylamines, pharmaceuticals, and alkaloids but remarkably also allows the lowest catalyst loading (0.00001 mol% or 0.1 ppm) ever reported for an organic dye. Bruylants reactions and C-alkylation/decyanations were performed on the obtained α-aminonitriles to demonstrate the postfunctio…

AlkylationLightMolecular Structure010405 organic chemistryChemistryOrganic ChemistryTotal synthesisActive systemsGeneral ChemistryAlkylationIsoquinolines010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysisAlkaloidsMetal freeMetalsPhotocatalysisOrganic chemistryMoleculeAminesOxidation-ReductionVisible spectrumChemistry - A European Journal
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Current therapeutical strategies for allergic rhinitis

2018

Allergic rhinitis is a common condition with increasing prevalence and is associated with several comorbid disorders such as bronchial asthma and atopic dermatitis. If allergen avoidance is not possible, allergen-specific immunotherapy is the only causal treatment option.This review focuses on current treatments and the future outlook for allergic rhinitis. Pharmacotherapy includes mast cell stabilizers, antihistamines, glucocorticosteroids (GCSs), leukotriene receptor antagonists, and nasal decongestants. Nasal GCSs are currently regarded as the most effective treatment and are considered first-line therapy together with non-sedating antihistamines. The new formulation MP29-02 combines the…

Allergen immunotherapyRhinitis allergicTreatment outcomeHistamine Antagonistsmacromolecular substancesmedicine.disease_cause03 medical and health sciences0302 clinical medicineAllergenimmune system diseasesmedicineHumansPharmacology (medical)AsthmaPharmacologybusiness.industryHistamine antagonistsGeneral MedicineAtopic dermatitisrespiratory systemmedicine.diseaseRhinitis Allergicrespiratory tract diseasesbody regionsTreatment OutcomeDesensitization Immunologic030220 oncology & carcinogenesisImmunologybusiness030217 neurology & neurosurgeryExpert Opinion on Pharmacotherapy
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Mast cells in allergic asthma and beyond.

2010

Mast cells have been regarded for a long time as effector cells in IgE mediated type I reactions and in host defence against parasites. However, they are resident in all environmental exposed tissues and express a wide variety of receptors, suggesting that these cells can also function as sentinels in innate immune responses. Indeed, studies have demonstrated an important role of mast cells during the induction of life-saving antibacterial responses. Furthermore, recent findings have shown that mast cells promote and modulate the development of adaptive immune responses, making them an important hinge of innate and acquired immunity. In addition, mast cells and several mast cell-produced me…

AllergyLeukotrienesmast cellsReview ArticleImmunoglobulin EModels BiologicalClassical complement pathwaychemistry.chemical_compoundMiceImmune systemAnti-Infective AgentsThymic Stromal LymphopoietinmedicineHypersensitivityAnimalsHumansmediatorsInnate immune systembiologyTumor Necrosis Factor-alphaGeneral MedicineImmunoglobulin Emedicine.diseaseAcquired immune systemallergyAsthmachemistryImmune SystemImmunologybiology.proteinProstaglandinsCytokinesTumor necrosis factor alphaHistamineHistamineYonsei medical journal
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Design, Synthesis, and Biological Evaluation of Novel Fluorinated Ethanolamines

2011

The preparation of novel fluorinated allylamines and their use as key fragments for the stereoselective synthesis of hydroxyethyl secondary amine (HEA)-type peptidomimetics is described. Our strategy employs chiral sulfinyl imines as synthesis intermediates, by treatment of hemiaminal precursors with two equivalents of vinylmagnesium bromide. The subsequent oxidation of the allylic amines to the corresponding epoxides was achieved by treatment with methyl(trifluoromethyl)dioxirane. Finally, epoxide ring opening with a range of nitrogen nucleophiles provided a library of HEA-derived peptidomimetics with a phenyldifluoromethylene moiety. The biological evaluation of these derivatives revealed…

Allylic rearrangementHalogenationPhthalic AcidsSulfonium CompoundsEpoxideCatalysisNocardiaantimicrobialsMycobacteriumchemistry.chemical_compoundDioxiraneNucleophileAnti-Infective AgentsfluorineMoietyOrganic chemistryAspartic Acid EndopeptidasesHumansEthanolamineTrifluoromethylMolecular StructureAntimicrobialsOrganic ChemistryEthanolaminesStereoisomerismBACE1FluorineGeneral ChemistrychemistryEthanolaminespeptidomimeticsHemiaminalethanolaminesEpoxy CompoundsIminesPeptidomimeticsAmyloid Precursor Protein Secretases
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Novel Approach for Asymmetric Synthesis of Fluorinated β-Amino Sulfones and Allylic Amines

2003

[reaction: see text] Enantiomerically pure gamma-fluoroalkyl beta-amino sulfones are readily synthesized in three steps starting from fluorinated imidoyl chlorides and arylmethyl sulfones. A complementary two-step sequence starting from chiral fluorinated beta-amino sulfoxides has also been developed. To illustrate the application of this procedure, a new method for the synthesis of alpha-fluoroalkyl allylic amines in optically pure form involving a Julia methylenation-desulfonylation reaction is presented.

Allylic rearrangementHydrocarbons FluorinatedChemistryorganic chemicalsOrganic ChemistryEnantioselective synthesisStereoisomerismGeneral MedicineCombinatorial chemistryBiochemistryAllyl CompoundsOrganic chemistrySulfonesAminesPhysical and Theoretical ChemistryOrganic Letters
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