Search results for "Moiety"

showing 10 items of 621 documents

Solution versus Fluorous versus Solid-Phase Synthesis of 2,5-Disubstituted 1,3-Azoles. Preliminary Antibacterial Activity Studies

2009

A small library of compounds with an oxa(thia)zole scaffold and structural diversity in both positions 2 and 5 has been synthesized. Double acylation of a protected glycine affords intermediate α-amido-β-ketoesters, which in turn can be dehydrated to afford 1,3-oxazoles or reacted with Lawesson’s reagent to furnish 1,3-thiazoles. This procedure was designed with its adaptation to fluorous techniques in mind. Thus, when a protected glycine with a fluorous tag in the ester moiety is used as a starting material, the synthesis can be easily completed without column chromatography purification of intermediate compounds with good to excellent yields, thus affording a suitable entry to the prepara…

AzolesStaphylococcus aureusANTIBACTERIAL ACTIVITYDrug Evaluation PreclinicalMicrobial Sensitivity TestsChemical synthesisSmall Molecule LibrariesAcylationchemistry.chemical_compoundSolid-phase synthesisColumn chromatographyAZOLESOrganic chemistryMoietyAntibacterial agentChemistryOrganic ChemistryCiencias QuímicasFLUOROUSCombinatorial chemistryAnti-Bacterial AgentsSolutionsQuímica OrgánicaMolecular ProbesSOLID-PHASELawesson's reagentAntibacterial activityCIENCIAS NATURALES Y EXACTAS
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Naphthyridine Derivatives as a Model System for Potential Lithium-Sulfur Energy-Storage Applications

2015

Naphthyridines have been identified as structural elements in sulfurized polyacrylonitrile, which is a common electrode material in lithium–sulfur batteries. Some dibenzonaphthyridine derivatives with a fused dithiolo moiety were prepared as model compounds for battery studies. These heterocyclic systems were prepared via the corresponding diphenyldicarbamide intermediate. Followed by naphthyridione formation, stepwise installation of the dithiolane subunit occurred in a straightforward manner. In the solid state, the heteroaromatic system is completely planar and was thoroughly characterized. Initial battery cycling tests indicated a potential use of such structural motifs in sulfur–lithiu…

Battery (electricity)Organic ChemistryPolyacrylonitrilechemistry.chemical_elementElectrochemistryCombinatorial chemistrySulfurEnergy storageDithiolanechemistry.chemical_compoundchemistryMoietyOrganic chemistryLithiumPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Crystal structure of 5-(5,6-dihydrobenzo[4,5]imidazo[1,2-c]quinazolin-6-yl)-2-methoxyphenol

2015

In the molecule of the title compound, C21H17N3O2, the 5,6-dihydrobenzimidazo[1,2-c]quinazoline moiety is disordered over two orientations about a pseudo-mirror plane, with a refined occupancy ratio of 0.863 (2):0.137 (2). The dihedral angles formed by the benzimidazole ring system and the benzene ring of the quinazoline group are 14.28 (5) and 4.7 (3)° for the major and minor disorder components, respectively. An intramolecular O—H...O hydrogen bond is present. In the crystal, molecules are linked by O—H...N hydrogen bonds, forming chains running parallel to [10-1].

Benzimidazolecrystal structurecyclizationCrystallographyHydrogen bondGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsRing (chemistry)BioinformaticsMedicinal chemistryData Reportschemistry.chemical_compoundchemistryQD901-999QuinazolineMoietyGeneral Materials Scienceimidazole derivativeBenzeneActa Crystallographica Section E: Crystallographic Communications
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1H and 13C NMR investigation of the fluxional behavior of η6-(bicyclo[6.1.0]Nona-2,4,6-triene)hexacarbonyldiiron- (FeFe)

1977

Abstract The variable temperature 1 H and 13 C NMR spectra of (C 9 H 10 )Fe 2 (CO) 6 have been recorded. The molecule is fluxional. The high temperature spectra indicate an apparent plane of symmetry bisecting the bound organic ligand, whereas the low temperature limiting spectra are entirely consistent with the asymmetric skew-type structure found in the crystal. Thus the molecule is also properly described in solution as μ-(2-σ,6,7-η:35-η-bicyclo[6.1.0]nonatriene)hexacarbonyldiiron(FeFe). Based on the observed line shape changes of the carbonyl resonances between −140 and −110°C, it is shown that the twitching and not the gliding process is responsible for the relative movement of the F…

Bicyclic moleculeChemistryStereochemistryLigandChemical shiftOrganic ChemistryCarbon-13 NMRRing (chemistry)BiochemistrySpectral lineInorganic ChemistryCrystallographyMaterials ChemistryMoietyMoleculePhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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How far the substituent effects in disubstituted cyclohexa-1,3-diene derivatives differ from those in bicyclo[2.2.2]octane and benzene?

2018

Substituents effects in cyclic diene derivatives are studied using quantum chemical modeling and compared to the corresponding effects in aromatic (benzene) and fully saturated (bicyclo[2.2.2]octane) compounds. In particular, electronic properties of the fixed group Y in a series of 3- and 4-X-substituted cyclohexa-1,3-diene-Y derivatives (where Y = NO2, COOH, COO− OH, O−, NH2, and X = NMe2, NH2, OH, OMe, Me, H, F, Cl, CF3, CN, CHO, COMe, CONH2, COOH, NO2, NO) are examined using the B3LYP/6-311++G(d,p) method. For this purpose, quantum chemistry models of the substituent effect: cSAR (charge of the substituent active region) and SESE (substituent effect stabilization energy) as well as trad…

Bicyclic moleculeDienesubstituent effects010405 organic chemistrymolecular modelingSubstituent010402 general chemistryCondensed Matter PhysicsResonance (chemistry)electronic structure01 natural sciencesQuantum chemistryMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundchemistrysubstituent effect stabilization energyMoietyPhysical and Theoretical ChemistryBenzenecharge of the substituent active regionOctaneStructural Chemistry
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Synthesis and biological evaluation of new bicyclic fluorinated uracils through ring-closing metathesis.

2006

Two families of bicyclic fluorinated uracils have been prepared starting from a gem-difluorinated unsaturated nitrile, by means of a ring-closing metathesis reaction to form the new ring, which is fused at the C-5/C-6 or N-1/C-6 positions of the uracil moiety. The selective formation of olefin regioisomers in the metathesis process can be controlled according to the reaction conditions (catalyst, solvent, and temperature). The acaricidal activities of the resulting compounds have also been investigated.

Bicyclic moleculeNitrileMolecular StructureChemistryOrganic ChemistryGeneral MedicineFluorineRing (chemistry)MetathesisChemical synthesisCombinatorial chemistrychemistry.chemical_compoundRing-closing metathesisSalt metathesis reactionOrganic chemistryRing-opening metathesis polymerisationMoietyUracilAcyclic diene metathesisThe Journal of organic chemistry
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Synthesis of new, UV-photoactive dansyl derivatives for flow cytometric studies on bile acid uptake.

2009

Four new fluorescent derivatives of cholic acid have been synthesized; they incorporate a dansyl moiety at 3 alpha-, 3 beta-, 7 alpha- or 7 beta- positions. These cholic acid analogs are UV photoactive and also exhibit green fluorescence. In addition, they have been demonstrated to be suitable for studying the kinetics of bile acid transport by flow cytometry.

Bile acid transportmedicine.drug_classPhotochemistryUltraviolet RaysKineticsMolecular ConformationBiochemistryFluorescenceFlow cytometrychemistry.chemical_compoundfluids and secretionsmedicinepolycyclic compoundsMoietyAnimalsPhysical and Theoretical ChemistryDansyl CompoundsChromatographyBile acidmedicine.diagnostic_testOrganic ChemistryCholic acidCholic AcidsStereoisomerismFlow CytometryFluorescenceRatsKineticschemistryLiverOrganicbiomolecular chemistry
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Combined heterologies for monoclonal antibody-based immunoanalysis of fluxapyroxad

2018

Nowadays, instrumental methodologies and rapid bioanalytical techniques complement each other for the analysis of toxic chemical compounds. Fluxapyroxad was commercialized a few years ago as a fungicide and today it is being used worldwide to control a variety of pests. In the present study, the development of monoclonal antibody-based immunochemical methods for the analysis of this chemical in food samples was evaluated for the first time. Novel haptens were synthesized and protein bioconjugates were prepared. High-affinity and specific monoclonal antibodies to fluxapyroxad were generated from two haptens with alternative linker tethering sites. Haptens with linker site heterology and a st…

Bioanalysismedicine.drug_classEnzyme-Linked Immunosorbent AssayFood ContaminationFluxapyroxadMonoclonal antibody01 natural sciencesBiochemistryAnalytical ChemistryMice0404 agricultural biotechnologyLimit of DetectionElectrochemistrymedicineIc50 valuesAnimalsEnvironmental ChemistryMoietySpectroscopyChromatographymedicine.diagnostic_testChemistry010401 analytical chemistryAntibodies Monoclonal04 agricultural and veterinary sciencesAmides040401 food scienceFungicides Industrial0104 chemical sciencesFruitImmunoassayPyrazolesHaptensHaptenLinkerThe Analyst
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Biphenyl derivatives containing trimethylsilyl benzyl ether or oxime groups as probes for NO2 detection

2016

[EN] Four probes based in the use of a biphenyl moiety and functionalized with trimethylsilyl benzyl ether (P1 and P3) and oxime (P2 and P4) groups have been prepared and tested as optical probes for the detection of NO2. Reaction of NO2 with acetonitrile solutions of P2-P4 resulted in the formation of aldehydes 7 and 8 with a concomitant redshift of the absorption bands. Probe P2 displayed a bathochromic shift of 45 nm upon reaction with NO2 and was able to detect this poisonous gas at concentrations as low as 0.02 ppm. P2 was highly selective against NO2 and other gases (i.e. NO, CO2, H2S, SO2) and vapours of organic solvents (i.e. acetone, hexane, chloroform, acetonitrile or toluene) had…

BiphenylChloroformTrimethylsilyl010405 organic chemistryGeneral Chemical EngineeringQUIMICA INORGANICAGeneral Chemistry010402 general chemistryOxime01 natural sciencesMedicinal chemistryToluene0104 chemical scienceschemistry.chemical_compoundQUIMICA ORGANICAchemistryBathochromic shiftOrganic chemistryMoietyAcetonitrile
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4,4′-Substituted biphenyl coronands. Preparation of a new selective fluorescent sensor for mercury salts

2006

Six new 4,4′-substituted biphenyl coronands have been prepared. The ligands containing dimethylamino groups in the biphenyl moiety have been used in transition metal cations’ complexation and one of them (3) has demonstrated to be a selective fluorescent sensor for mercury. Stoichiometries of the formed complexes and complexation constants have been determined by titration experiments. In addition, the extractant ability of some ligands has also been studied. Finally, the electrochemical properties of some of these ligands are also described.

BiphenylOrganic ChemistryInorganic chemistrychemistry.chemical_elementElectrochemistryBiochemistryFluorescenceMercury (element)chemistry.chemical_compoundchemistryTransition metalDrug DiscoveryMoietyTitrationStoichiometryTetrahedron
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