Search results for "química orgánica"

showing 10 items of 87 documents

Metal-atom impact on the self-assembly of cup-and-ball metalloporphyrin–fullerene conjugates

2014

International audience; A fullerene ammonium derivative has been combined with different metalloporphyrin–crown ether receptors to generate very stable supramolecules. The combination of fullerene–porphyrin and ammonium–crown ether interactions leads to a strong chelate effect as evidenced by a high effective molarity (3.16 M). The different parameters influencing the stability of the supramolecular ensembles, in particular the nature of the metal in the porphyrin moiety, have been rationalized with the help of theoretical calculations thus providing new insights into fullerene–porphyrin interactions.

FullereneMolecular model010405 organic chemistrySupramolecular chemistryQuímica orgánicaEtherGeneral ChemistryGeneral Medicine010402 general chemistryPorphyrin01 natural sciencesCatalysis0104 chemical sciencesMetalchemistry.chemical_compoundchemistryComputational chemistryvisual_artEffective molarityvisual_art.visual_art_mediumMoietyOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistry
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Bis(imidazolium) salts derived from amino acids as receptors and transport agents for chloride anions

2015

The binding properties of bis(imidazolium) hosts 1a–c derived from amino acids towards different anions have been studied by 1H NMR titration experiments in 95 : 05 CD3CN : H2O at 303 K, ESI-MS and theoretical calculations. Among this family, the salt 1c showed a strong and high selectivity for chloride anions. Transmembrane chloride transport activity has also been studied for the three bis(imidazolium) based transporters in POPC liposome models, and compound 1a was identified as an active chloride/nitrate exchanger.

General Chemical EngineeringChemistry OrganicSalt (chemistry)Medicinal chemistryChlorideCompostos orgànics Síntesichemistry.chemical_compoundmedicineLife ScienceOrganic chemistryPOPCVLAGchemistry.chemical_classificationLiposomeamino acidsOrganic Chemistrychloride anionsQuímica orgánicaGeneral ChemistryOrganische ChemieTransmembrane proteinAmino acidchemistryProton NMRbis(imidazolium)TitrationAminoàcidsmedicine.drug
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Lipase-catalysed preparation of acyl derivatives of the germacranolide cnicin

2009

Several acyl derivatives of cnicin were obtained through lipase-catalysed acylation and alcoholysis reactions. In most reactions lipases showed a regioselective behaviour affording only one product. Longer chain acyl derivatives were prepared at lower temperature than the used in lipase-catalysed reactions, to preclude side products formation. The enzymatic approach let to prepare a family of novel acetyl and fatty acid derivatives of cnicin which are not obtainable following traditional organic synthetic procedures. Fil: Monsalve, Leandro Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis…

GermacranolideTriacylglycerol lipaseBioengineeringBiochemistryCnicinCatalysisEnzyme catalysisAcylationchemistry.chemical_compoundOrganic chemistryLipasechemistry.chemical_classificationbiologyENZYME CATALYSISChemistryProcess Chemistry and TechnologyCiencias QuímicasRegioselectivityALCOHOLYSISCNICINACYLATIONSESQUITERPENOIDSEnzymeQuímica Orgánicabiology.proteinCIENCIAS NATURALES Y EXACTAS
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A Bipyridine‐Palladium Derivative as General Pre‐Catalyst for Cross‐Coupling Reactions in Deep Eutectic Solvents

2019

A versatile and DES‐compatible bipyridine palladium complex has been developed as a general pre‐catalyst for different cross‐coupling reactions (Hiyama, Suzuki‐Miyaura, Heck‐Mizoroki and Sonogashira) in deep eutectic solvents. Hydrogen bond capacity of the ligand allows to keep the excellent level of results previously obtained in classical organic solvents. Palladium pre‐catalyst showed a high catalytic activity for many cross‐coupling reactions, demonstrating a great versatility and applicability. Also, this methodology employs sustainable solvents as a reaction medium and highlights the potential of DES as alternative solvents in organometallic catalysis. The catalyst and DES were easily…

Green chemistry010405 organic chemistryHydrogen bondchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCoupling reaction0104 chemical sciencesCatalysisHydrogen bondsLigand designchemistry.chemical_compoundBipyridineQuímica OrgánicachemistryGreen chemistryPolymer chemistryCross-couplingDerivative (chemistry)PalladiumEutectic systemPalladium
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Intra- and extra-cellular DNA damage by harmine and 9-methyl-harmine

2014

It is known that b-carbolines are able to produce photosensitized damage in cell-free DNA, but there is little information on their effects on cellular DNA. Therefore, we have analyzed the DNA damage produced by harmine and 9-methyl-harmine under UVA irradiation in V79 cells, together with the associated generation of micronuclei and photocytotoxicity. The results indicate that the most frequent photoproducts generated in the cellular DNA are modified purines such as 8-oxo-7,8-dihydroguanine. Only relatively few single-strand breaks were observed. CPDs were absent, although they were generated in cell-free DNA irradiated under the same conditions. The overall extent of DNA damage in the cel…

Guanineb-carbolinesUltraviolet RaysDNA damageBiophysicsFree radical damage to DNACHO CellsMicronucleiBiologyPhototoxicitychemistry.chemical_compoundCricetulusHarmineCyclobutane pyrimidine photodimersCricetinaeAnimalsRadiology Nuclear Medicine and imagingPurine metabolismRadiationRadiological and Ultrasound TechnologyCell growthOtras Ciencias QuímicasCiencias QuímicasDNAHydrogen-Ion ConcentrationHarmineQuímica OrgánicaBiochemistrychemistryMicronucleus testBiophysicsPhotosensitizationPhototoxicityCIENCIAS NATURALES Y EXACTASDNADNA DamageJournal of Photochemistry and Photobiology B: Biology
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Pyridylcarbene formation by thermal decomposition of 7-bromo-3-methyl-[1,2,3]triazolo[1,5-a]pyridine under pressure

2007

7-Bromo-3-methyl-[1,2,3]triazolo[1,5-a]pyridine 1 at 1.7 atm and 100ºC decompose to form a pyridylcarbene intermediate by nitrogen expulsion. The carbene stabilization give 2-bromo-6- vinylpyridine 2, 1-(6-bromopyridin-2-yl)ethanol 3, 1-(6-Bromopyridin-2-yl)ethanone 4, 2- bromo-6-[2-(6-bromopyridin-2-yl)-2-methyl-trans-cyclopropyl]pyridine 5, and 2-bromo-6-[2-(6- bromopyridin-2-yl)-2-methyl-cis-cyclopropyl]pyridine 6. Abarca Gonzalez, Belen, Belen.Abarca@uv.es ; Ballesteros Campos, Rafael, Rafael.Ballesteros@uv.es

High pressure reactionEthanolPyridylcarbeneUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Organic ChemistryThermal decompositionchemistry.chemical_element:QUÍMICA [UNESCO]Medicinal chemistryNitrogenlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrychemistryTriazolopyridines decompositionPyridinePyridylcarbene ; High pressure reaction ; Triazolopyridines decompositionOrganic chemistryUNESCO::QUÍMICA::Química orgánicaCarbeneArkivoc
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An efficient synthesis of new fluorinated uracil derivatives.

2003

A series of potentially biologically active fluorinated uracil derivatives has been prepared in three steps from oxazolines and fluorinated nitriles with good chemical yields. Fustero Lardies, Santos, Santos.Fustero@uv.es ; Sanz Cervera, Juan Francisco, Juan.F.Sanz@uv.es ; Asensio Martinez, Amparo, Amparo.Asensio@uv.es

Hydrocarbons FluorinatedSynthesis ; Fluorinated uracil derivatives ; Oxazolines ; Biologically activeAntimetabolitesUNESCO::QUÍMICABiologically active:QUÍMICA::Química orgánica [UNESCO]UracilGeneral MedicineOxazolines:QUÍMICA [UNESCO]Combinatorial chemistryFluorinated uracil derivativesSynthesischemistry.chemical_compoundchemistryNitrilesUNESCO::QUÍMICA::Química orgánicaUracilOxazolesChemical communications (Cambridge, England)
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Experimental and theoretical studies on polar Diels–Alder reactions of 1-nitronaphathalene developed in ionic liquids

2013

The reactions between 1-nitronaphthalene 1 and two nucleophilic dienes, Danishefsky´s diene 2 and 1-trimethylsilyloxy-1,3-butadiene 3, to yield phenanthrenols 7 and 8 developed in protic and aprotic ionic liquids (ILs) with an imidazolium cation base permit to conclude that the reactions occur in better experimental conditions than in molecular solvents. The yields obtained with protic ILs are better than those observed with aprotic ILs. In this sense, the higher yields obtained with aprotic ILs, (working at 60ºC, 48 h) are comparable with the lower yields observed in protic ILs (60 ºC, 24 h). DFT calculations for the reaction of 1-nitronaphthalene 1 with diene 3, in the absence and in the …

IONIC LIQUIDTetrafluoroborateDieneGeneral Chemical EngineeringSolvationCiencias QuímicasGeneral ChemistryNitrosoPhotochemistryNITRONAPHTHALENESDFTDIELS-ALDERCatalysischemistry.chemical_compoundQuímica OrgánicachemistryNucleophileComputational chemistryIonic liquidSolvent effectsCIENCIAS NATURALES Y EXACTAS
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Indole-substituted 2,4-diamino-5,8-dihydropyrido[2,3-d]pyrimidines from one-pot process and evaluation of their ability to bind dopamine receptors

2018

A series of novel 7-indole substituted 2,4-diamino-5,8-dihydropyrido[2,3-d]pyrimidine analogous to the 2,4-diaminopteridine core were synthesized by the three-component one-pot cyclocondensation between 2,4,6-triaminopyrimidine, 3-(2-cyanoacetyl)indole and aromatic aldehydes. The reactions, which exhibited good performance, proceeded in EtOH using indium (III) chloride as catalyst under microwave irradiation, in short reaction times. On the basis of certain structural similarity of these compounds with known ligands of the D2 dopamine receptors (D2DR), the study of these compounds as possible ligands of dopamine D2 and D1 receptors was carried out. Three of them showed moderate affinity to …

Indole testPYRIDOPYRIMIDINE010405 organic chemistryChemistryStereochemistryOrganic ChemistryCiencias QuímicasTHREE-COMPONENT SYNTHESIS010402 general chemistryBIND DOPAMINE01 natural sciencesBiochemistry0104 chemical sciencesQuímica OrgánicaD1 AND D2 RECEPTORSDopamine receptorDrug DiscoveryMOLECULAR MODELINGCIENCIAS NATURALES Y EXACTASTetrahedron
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Diels-Alder reaction between indoles and cyclohexadienes photocatalyzed by a (thia)pyrylium salt

2007

"Thiapyrylium salt 1 is an efficient photocatalyst in the Diels-Alder reaction between indoles (InHs) and 1,3-cyclohexadienes (CHDs). For instance, irradiation of deaerated dichloromethane solutions containing 1 (1 mM), indole (20 mM) and cyclohexadiene (40 mM), in the presence of an acylating agent, led to the Diels-Alder cycloadduct in 62% yield (endo:exo ratio of 1.8:1). Taking into account the very high intersystem crossing yield (Φisc = 0.97) of thiapyrylium salt 1, involvement of its triplet excited state in this Diels-Alder reaction has been studied using steadystate and time-resolved experiments; the results are compared with those previously obtained for pyrylium salts, which exhib…

Indoles 1.3-cyclohexadienesUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Diels-Alder reaction ; Photocatalysis ; Thiapyrylium salts ; Indoles 1.3-cyclohexadienesUNESCO::QUÍMICA::Química orgánicaPhotocatalysisDiels-Alder reaction:QUÍMICA [UNESCO]Thiapyrylium salts
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