Search results for "thiourea"

showing 10 items of 96 documents

Organocatalytic Enantioselective Synthesis of Pyrazoles Bearing a Quaternary Stereocenter

2016

An efficient one-pot asymmetric synthesis of pyrazoles bearing a chiral quaternary stereocenter has been developed. Quinine-derived thiourea catalyzed the enantioselective addition of pyrazolones to isatin-derived ketimines, providing the corresponding acetylated pyrazoles after in situ treatment with Ac2O/Et3N. The corresponding pyrazoles were afforded in high yields and excellent enantioselectivities.

Isatin-derived ketimines010402 general chemistry01 natural sciencesBiochemistryCatalysisStereocenterchemistry.chemical_compoundCatàlisiCompostos orgànicsAsymmetric catalysisOrganic chemistryOrganocatalysis010405 organic chemistryChemistryEstereoquímicaOrganic ChemistryEnantioselective synthesisGeneral ChemistryQuaternary stereocenters0104 chemical sciencesThioureaFISICA APLICADAOrganocatalysisPyrazolesPyrazolonesQuímica orgànica
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Effects of K(ATP) channel modulators on acetylcholine release from guinea-pig isolated atria and small intestine.

2002

The effects of K(ATP) channel blockers (glibenclamide, HMR 1883, HMR 1372) and openers (cromakalim, pinacidil, diazoxide) on the electrically-evoked (5 Hz) release of [(3)H]acetylcholine were studied in isolated guinea-pig atria and myenteric plexus-longitudinal muscle preparations which had been preincubated with [(3)H]choline. Atria: Cromakalim (0.3 microM and 1 microM), pinacidil (10 microM) and diazoxide (30 microM) significantly reduced the stimulation-evoked release of [(3)H]acetylcholine. The inhibition produced by cromakalim and pinacidil was prevented by 1 microM of either HMR 1883, HMR 1372 or glibenclamide. The blockers alone significantly increased the release at concentrations …

MaleCromakalimPotassium ChannelsGuinea PigsNeuromuscular JunctionMyenteric PlexusPharmacologyIn Vitro Techniqueschemistry.chemical_compoundGlyburideIntestine SmallmedicineDiazoxidePotassium Channel BlockersAnimalsChannel blockerHeart AtriaPharmacologySulfonamidesPinacidilDiazoxideThioureaPotassium channel blockerMuscle SmoothGeneral Medicinemusculoskeletal systemAtrial FunctionMyocardial ContractionHMR 1883Potassium channelAcetylcholinechemistryAnesthesiaPinacidilcardiovascular systemFemaleCromakalimAcetylcholinemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Responses to histamine and selective H2-receptor agonists in lung parenchymal strips from normal and sensitized guinea-pigs.

1989

Histamine produces concentration-dependent contractions of lung parenchyma strips obtained from normal and sensitized guinea-pigs. The responsiveness of the sensitized lung strips to histamine was significantly increased compared to normal tissues. Clemizole (0.1 microM) was equally effective as an H1-antagonist in normal (dose-ratio 9.12) and sensitized (dose-ratio 9.77) tissues. The concentration-response curves to histamine were displaced to the left by cimetidine (0.1 microM to 0.1 mM) with similar dose-ratios in normal and sensitized tissues. Cimetidine enhanced maximal responses to histamine only in normal lung strips. The effects of submaximal equieffective concentrations of histamin…

Malemedicine.medical_specialtyImmunologyGuinea PigsToxicologyGuanidineschemistry.chemical_compoundImpromidineHistamine H2 receptorDimapritInternal medicineParenchymamedicineAnimalsPharmacology (medical)Receptors Histamine H2CimetidineLungPharmacologyLungDose-Response Relationship Drugbusiness.industryMethylhistaminesImidazolesIsoproterenolThioureaMuscle SmoothImpromidineDimapritClemizolemedicine.anatomical_structureEndocrinologychemistryBenzimidazolesbusinessCimetidineHistaminemedicine.drugHistamineMuscle ContractionAgents and actions
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Structural and Optical Study of Ga3+ Substitution in CuInS2 Nanoparticles Synthesized by a One-Pot Facile Method

2014

A one-pot method was used to synthesize CuInxGa1–xS2 nanoparticles by substituting In3+ with Ga3+. The samples with composition of gallium ranging from 0% to 100% were synthesized by solving copper chloride, indium trichloride, gallium acetylacetonate, and thiourea as precursors in 1-octadecene, oleylamine, and oleic acid as noncoordinating, coordinating, and capping agent solvents, respectively. Depending on the chemical composition and synthesis conditions, the morphology of the as-synthesized nanoparticles obtained was trigonal, semitrigonal, hexagonal, and quasi-spherical. X-ray photoelectron spectroscopy and X-ray diffraction confirmed that Ga3+ substituted In3+ without any segregation…

Materials scienceBand gapInorganic chemistrychemistry.chemical_elementNanoparticleSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergychemistryX-ray photoelectron spectroscopyThioureaOleylaminePhysical and Theoretical ChemistryGalliumCopper chlorideGallium acetylacetonateNuclear chemistryThe Journal of Physical Chemistry C
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Structural and optical properties of Fe and Zn substituted CuInS2 nanoparticles synthesized by a one-pot facile method

2015

We substitute indium present in the CuInS2 ternary compound by iron and zinc using a facile one-pot synthesis method. The quaternary compound of CuIn1−xMxS2 (M = Fe and Zn) was synthesized by dissolving CuCl, InCl3, FeCl3, Zn(ac)2 and SC(NH2)2 as precursors in 1-octadecene, oleylamine and oleic acid as non-coordinating, coordinating and capping agent solvents, respectively. Oleic acid, oleylamine and thiourea were used respectively as a hard Lewis base, borderline Lewis base (in comparison with oleic acid) and soft Lewis base to form appropriate complexes. The complex formation, structure, and optical properties of CuIn1−xMxS2 (M = Fe and Zn) nanoparticles were studied by Fourier transform …

Materials scienceInorganic chemistrychemistry.chemical_elementGeneral ChemistryZincchemistry.chemical_compoundchemistryThioureaX-ray photoelectron spectroscopyTernary compoundOleylamineMaterials ChemistryLewis acids and basesFourier transform infrared spectroscopySpectroscopyJournal of Materials Chemistry C
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Enhanced bistability by guest inclusion in Fe(ii) spin crossover porous coordination polymers

2012

Inclusion of thiourea guest molecules in the tridimensional spin crossover porous coordination polymers {[Fe(pyrazine)[M(CN)(4)]} (M = Pd, Pt) leads to novel clathrates exhibiting unprecedented large thermal hysteresis loops of ca. 60 K wide centered near room temperature.

Materials sciencePyrazineStereochemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHysteresischemistry.chemical_compoundCrystallographychemistryThioureaSpin crossoverMaterials ChemistryCeramics and CompositesMoleculePlatinumThermal analysisPalladiumChemical Communications
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Enantioselective Mannich reaction of β-keto esters with aromatic and aliphatic imines using a cooperatively assisted bifunctional catalyst

2014

An efficient urea-enhanced thiourea catalyst enables the enantioselective Mannich reaction between β-keto esters and N-Boc-protected imines under mild conditions and minimal catalyst loading (1–3 mol %). Aliphatic and aromatic substituents are tolerated on both reaction partners, affording the products in good enantiomeric purity. The corresponding β-amino ketones can readily be accessed via decarboxylation without loss of enantiomeric purity.

Molecular StructureChemistryDecarboxylationOrganic ChemistryEnantioselective synthesisThioureaEstersStereoisomerismKetonesBiochemistryDecarboxylationCatalysisCatalysisBifunctional catalystchemistry.chemical_compoundThioureaOrganic chemistryUreaIminesPhysical and Theoretical ChemistryEnantiomerMannich reactionta116Organic Letters
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Stereoselective Synthesis and Cytoselective Toxicity of Monoterpene-Fused 2-Imino-1,3-thiazines

2014

Starting from pinane-, apopinane- and carane-based 1,3-amino alcohols obtained from monoterpene-based β-amino acids, a library of monoterpene-fused 2-imino-1,3-thiazines as main products and 2-thioxo-1,3-oxazines as side-products were prepared via two- or three-step syntheses. When thiourea adducts prepared from 1,3-amino alcohols and aryl isothiocyanates were reacted with CDI under mild conditions, O-imidazolylcarbonyl intermediates were isolated which could be transformed to the desired 1,3-thiazines under microwave conditions. 1,3-Thiazines and 2-thioxo-1,3-oxazine side-products could also be prepared in one-step reactions through the application of CDI and microwave irradiation. The rin…

MonoterpeneMolecular ConformationThiazinesPharmaceutical ScienceStereoisomerismArticleAnalytical ChemistryAdductHeLalcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryantiproliferativeCell Line TumorDrug DiscoveryOrganic chemistryHumansPhysical and Theoretical Chemistryta116Cell ProliferationbiologystereoselectiveArylOrganic Chemistry13-thiazineStereoisomerismbiology.organism_classificationCycloalkanechemistryThiourea13-amino alcoholChemistry (miscellaneous)MonoterpenesMolecular MedicineStereoselectivityCDImonoterpeneMolecules
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Synthesis of Pyrrolo-Condensed Derivatives with Potential Antiviral Activity

2014

NITROPHENYL-1H-PYRROLO[23-c]PYRIDINE DERIVATIVESAntiviral ActivitySettore CHIM/08 - Chimica FarmaceuticaBromopyridinethyilthioureaisoindolo[21-a]quinoxaline
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CCDC 1469018: Experimental Crystal Structure Determination

2016

Related Article: Filip Topić and Kari Rissanen|2016|J.Am.Chem.Soc.|138|6610|doi:10.1021/jacs.6b02854

Space GroupCrystallography(18-Crown-6) 1-methylthiourea 11223344-octafluoro-14-diiodobutaneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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