Search results for "imidazoline"

showing 3 items of 13 documents

Tandem Reactions of 1,2,4-Oxadiazoles with Allylamines

2011

A reaction of 3-chloro-1,2,4-oxadiazoles with allylamine and diallylamine has been investigated. 3,3a,4,5-Tetrahydroisoxazolo[3,4-d]pyrimidines are produced through a tandem ANRORC/[3 + 2]cycloaddition pathway consisting of the addition of allylamine to the 1,2,4-oxadiazole, followed by ring opening, nitrone formation, and finally cycloaddition. 3-N-Allylamino-1,2,4-oxadiazoles were also obtained as minor products through a classical SNAr. Conversely, a reaction with diallylamine produces 3-N,N-diallylamino-1,2,4-oxadiazole and imidazoline through tandem SNAr/aziridination and nucleophilic ring opening.

chemistry.chemical_classificationOxadiazolesMolecular StructureTandemChemistryOrganic ChemistryImidazoline receptorStereoisomerismSettore CHIM/06 - Chimica OrganicaRing (chemistry)BiochemistryMedicinal chemistryCycloadditionAllylamineAllylamineNitronechemistry.chemical_compoundANRORC Oxadiazoles cycloadditionsPyrimidinesNucleophileCyclizationNucleophilic aromatic substitutionPhysical and Theoretical Chemistry
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Firsts lysidinyl- and lysidinium-triphosphines Pd(II) complexes

2010

International audience; The preparation of first lysidinyl-triphosphine ligand (named Triphosline) is described in three steps which are first a Michael type addition of imidazolidine (or lysidine) to diethylvinylphosphonate, second a phosphonate reduction with LiAlH4 and third an anti-Markovnikov radical addition of the primary phosphine to diphenylvinylphosphine. The Triphosline behaves as a tridentate P-coordinating ligand in palladium(II) complexes. The dangling lysidine function is then cleanly and totally alkylated by methyl iodide to lead to a new kind of lysidinium-triphosphine complexes. Subsequent anion exchange with TlPF6 affords the first example of a chloride free lysidinium-tr…

imidazolinechemistry.chemical_elementpalladium complexesAlkylation010402 general chemistry01 natural sciencesimidazoleInorganic Chemistrychemistry.chemical_compoundImidazolidinetriphosphinePolymer chemistryMaterials ChemistryOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryLigand[ CHIM.COOR ] Chemical Sciences/Coordination chemistryPhosphonate0104 chemical scienceschemistryLysidinesynthesis of polyphosphinesPhosphinePalladiumMethyl iodidePolyhedron
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Identification of α2-adrenoceptors and non-adrenergic idazoxan binding sites in rabbit colon epithelial cells

1990

alpha 2-Adrenoceptors are possibly involved in the regulation of the hydroelectrolytic flux across the digestive mucosa. As no data are available concerning the existence of these receptors in colon epithelial cells, we aimed to investigate the existence of alpha 2-adrenoceptors in this tissue using tritiated antagonists. [3H]Yohimbine and [3H]rauwolscine were not usable to label colonic alpha 2-adrenoceptors because of their very high level of non-specific binding. In contrast, the methoxy derivative of idazoxan, [3H]RX821002, appeared a convenient radioligand for the purpose. [3H]RX821002 bound with high affinity (KD = 6.2 +/- 0.8 nM) to a single population of non-interacting sites (Bmax …

medicine.medical_specialtyColonRauwolscinePopulationAlpha (ethology)Imidazoline receptorIn Vitro TechniquesBinding CompetitiveEpitheliumDioxaneschemistry.chemical_compoundIdazoxanInternal medicinemedicineRadioligandAnimalsBinding siteReceptoreducationAdrenergic alpha-AntagonistsPharmacologyeducation.field_of_studyBinding SitesEpithelial CellsReceptors Adrenergic alphaMolecular biologyKineticsEndocrinologychemistryRabbitsIdazoxanmedicine.drugEuropean Journal of Pharmacology
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