Search results for "Thiazoline"

showing 4 items of 4 documents

Reaktionen von Benzothiet mit Iminen

1993

Reactions of Benzothiete with Imines A great variety of compounds 3a–w containing CN double bonds was studied in the reaction with benzothiete (1). H, alkyl, aryl, OR, SR and NR groups can be attached to the imino function. The azomethines 3a–f, the thiazolines 3g–i, the lactim 3n, the oximes 3r–t, the isoxazolinone 3u and the azine 3v show [8π + 2π] cycloaddition reactions yielding derivatives of 1,3-benzothiazine (4a–i, n, r–v). In the case of 4n, s, t secondary reactions occur, initiated by elimination processes. [8π + 2π] Cycloadditions account also for the reactions 3e 10, 11, 3o 18(I), and 3q 19; however, CC double bonds are representing the 2π component in these examples. The thiazol…

chemistry.chemical_classificationSteric effectsBicyclic moleculeDouble bondChemistryStereochemistryThiazolineOrganic ChemistryHydrazoneTautomerMedicinal chemistryCycloadditionAzinechemistry.chemical_compoundPhysical and Theoretical ChemistryLiebigs Annalen der Chemie
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Interaction of metal ions with D-glucobenzothiazoline: isolation and characterization of the resultant products

2002

Six different metal-ion complexes of D-glucobenzothiazoline were synthesized and characterized by analytical and spectral techniques. Formation of different types of species (ML and ML2) were observed with Cu2+, Ag+, Cd2+, Hg2+, and Zn2+ ions. Existence of an anomeric mixture in the case of the Cu2+ complex is identified from the EPR spectra, and the results were further supported by the simulated spectra. The structures were proposed based on different studies.

AnomerSilverStereochemistryMetal ions in aqueous solutionSynthesis (Chemical)BiochemistrySpectral lineAnalytical ChemistryD-glucobenzothiazolinelaw.inventionIonlawGlucobenzothiazolineBenzothiazolesElectron paramagnetic resonanceMercury (Metal)ChemistrySpectrum AnalysisOrganic ChemistrySpectrum AnalyzersElectron Spin Resonance SpectroscopyGeneral MedicineMercuryCharacterization (materials science)ThiazolesZincGlucoseMetalsPhysical chemistryStructure (Composition)CopperCadmiumIndraStra Global
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Avoidance and contextual learning induced by a kairomone, a pheromone and a common odorant in female CD1 mice

2015

Copyright © 2015 Fortes-Marco, Lanuza, Martínez-García and Agustín-Pavón.

Vomeronasal organPhysiologyPlace conditioningCD1Pheromoneslcsh:RC321-5712-heptanoneMicepheromoneAversionlcsh:Neurosciences. Biological psychiatry. NeuropsychiatryOriginal ResearchCommunicationbusiness.industryGeneral NeurosciencekairomoneContextual learning245-trimethylthiazolineIsoamyl acetateBiological significanceKairomoneSex pheromoneTMTPheromonePsychologybusinessVomeronasalNeuroscienceImmediate early geneKairomones
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CCDC 230604: Experimental Crystal Structure Determination

2004

Related Article: A.B.Gaspar, M.C.Munoz, J.A.Real|2004|Inorg.Chem.Commun.|7|815|doi:10.1016/j.inoche.2004.05.005

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[bis(mu~2~-Dicyanamide)-(mu~2~-44'-bipyridyl)-iron 22'-bithiazoline clathrate]Experimental 3D Coordinates
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