Search results for "MIDI"

showing 10 items of 1431 documents

A new strategy for the synthesis of fluorinated 3,4-dihydropyrimidinones

2009

A new family of 3,4-dihydropyrimidinones (DHPMs) bearing fluorinated substituents at C6 have been prepared from gem-difluorinated nitriles, alkyl 3-butenoates and iso(thio)cyanates. This novel Biginelli-type process relies on the gamma-addition of the ester-derived enolate to fluorinated nitriles. A tandem nucleophilic addition aza-Michael reaction sequence completes the synthetic process. (C) 2009 Elsevier B.V. All rights reserved.

chemistry.chemical_classificationNucleophilic additionFluorinated nitrilesTandemChemistryOrganic ChemistryThio-BiochemistryInorganic ChemistryReaction sequenceMulticomponent reactionsEnvironmental ChemistryOrganic chemistryFluorinated dihydropyrimidinonesPhysical and Theoretical ChemistryAlkylIntramolecular aza-Michael reaction
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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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Natural gas hydrates vs. induced dysfunctions in the hydrocarbon extraction process

2021

Cantoned fluids in porous-permeable or fractured media of reservoirs have acquired during the geological time special properties. The fluids from the reservoir could be or not a mixture of reservoir water, liquid hydrocarbons and gaseous hydrocarbons. Considering if inside of a reservoir there are two types of substances like natural gas and reservoir water which may be in the form of vaporous than the condition of saturation of gases with water vaporous is fulfilled. This process is taking place due to thermodynamic equilibrium resulting the so-called gas humidity. This state corroborated with a certain chemical composition plus favourable values of pressure and temperature may be decisive…

chemistry.chemical_classificationPetroleum engineeringThermodynamic equilibriumbusiness.industryClathrate hydrateHumidityEngineering (General). Civil engineering (General)HydrocarbonchemistryNatural gasExtraction (military)TA1-2040Saturation (chemistry)businessChemical compositionMATEC Web of Conferences
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Straightforward synthesis of bioconjugatable azo dyes. Part 1: Black Hole Quencher-​1 (BHQ-​1) scaffold

2014

Abstract Azo dyes are currently used to quench the fluorescence of energy donors in bioassays through Forster resonance energy transfer (FRET) phenomenon. Common examples of such dark quenchers are DABCYL and the three members of Black Hole Quencher® (BHQ) family. Yet, only carboxylic acid and phosphoramidite derivatives of such azo dyes are presently commercially available. This Letter presents a straightforward synthesis method to novel bioconjugatable quenchers derived from BHQ-1 scaffold and equipped with a reactive group being either azido, terminal alkyne, or maleimide. The potential utility of the ‘clickable’ azido and thiol-reactive derivatives was notably demonstrated through the p…

chemistry.chemical_classificationPhosphoramiditeBioconjugation[CHIM.ORGA]Chemical Sciences/Organic chemistryCarboxylic acidOrganic ChemistryAlkyneBlack Hole Quencher-1[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.THER]Chemical Sciences/Medicinal ChemistryPhotochemistry7. Clean energyBiochemistryFluorescence[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundFörster resonance energy transferchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryDrug DiscoveryMaleimideComputingMilieux_MISCELLANEOUS[CHIM.CHEM]Chemical Sciences/Cheminformatics
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Spermidine and morphogenesis in single cell cultures of Sideritis angustifolia lag.

1990

Abstract Single cells from hypocotyl-derived callus of Sideritis angustifolia were evaluated for morphogenesis when cultured in either solidifier or liquid Murashige and Skoog medium supplemented with various concentrations of spermidine, naphthaeneacetic acid (NAA), benzyladenine (BA) and dicyclohexylamine (DCHA). Spermidine (Spd) did not replace the hormonal requirements for cell division and callus formation, but affected growth induced by NAA or BA. This polyamine increased the plating efficiency of cells cultured in the presence of NAA (0.05, 0.54 and 5.40 μM) or BA (0.40, 4.40 and 8.80 μM). In contrast, Spd reduced growth induced by 10.80 μM NAA, optimal auxin concentration for callus…

chemistry.chemical_classificationPlating efficiencyCallus formationfungiPlant ScienceGeneral MedicineBiologySpermidinechemistry.chemical_compoundMurashige and Skoog mediumchemistryBiochemistryAuxinCallusmental disordersCytokininGeneticsPolyamineAgronomy and Crop SciencePlant Science
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Nucleotide, Nucleoside, Purine, Pyrimidine, Pteridine

1952

Die Organe erwachsener Tiere enthalten zumeist mehr Ribonucleotide als Desoxyribonucleotide (Tabelle 159). Der Quotient RN : DRN ist in fetalen Geweben kleiner als in erwachsenen. J. Geschwind und C. H. Li fanden ihn in der fetalen Rattenleber zu 0,9, in der Leber neugeborener Ratten zu 1,9 und in der Leber 40 Tage alter Ratten zu 2,8.

chemistry.chemical_classificationPyrimidine analogueTransition (genetics)chemistryPurine/pyrimidinePyrimidine metabolismmedicinePurine nucleoside phosphorylaseNucleotideMolecular biologyNucleosidePteridinemedicine.drug
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A new synthesis of soluble poly(1,4-phenylenevinylene)s and poly(2,5-pyrimidinylenevinylene)s

1991

Abstract Alkoxy-substituted 4-methylbenzylideneanilines 2a-f and their pyrimidine analogues 2g,h show an efficient selfcondensation in the alkaline medium KOC(CH 3 ) 3 /DMF. The totally stereoselective reaction yields 3a-h which are transformed by acidic work-up to 4a-h . A narrow distribution of the molecular weight can be achieved.

chemistry.chemical_classificationPyrimidine analoguechemistryOrganic ChemistryDrug DiscoveryPolymer chemistryOrganic chemistryStereoselectivityPolymerSelf-condensationBiochemistryTetrahedron Letters
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Halo and Pseudohalo Cu(I)-Pyridinato Double Chains with Tunable Physical Properties

2015

The properties recently reported on the Cu(I)-iodide pyrimidine nonporous 1D-coordination polymer [CuI(ANP)] (ANP = 2-amino-5-nitropyridine) showing reversible physically and chemically driven electrical response have prompted us to carry a comparative study with the series of [CuX(ANP)] (X = Cl (1), X = Br (2), X = CN (4), and X = SCN (5)) in order to understand the potential influence of the halide and pseudohalide bridging ligands on the physical properties and their electrical response to vapors of these materials. The structural characterization of the series shows a common feature, the presence of -X-Cu(ANP)-X- (X = Cl, Br, I, SCN) double chain structure. Complex [Cu(ANP)(CN)] (4) pre…

chemistry.chemical_classificationPyrimidineHydrogen bondChemistrySupramolecular chemistryHalideNanotechnologySingle chainPolymerInorganic ChemistryDouble chainchemistry.chemical_compoundCrystallographyPhysical and Theoretical ChemistryLuminescenceInorganic Chemistry
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7-Amino-2-methylsulfanyl-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxylic acid as the dimethylformamide and water monosolvates at 293 K.

2010

The molecular structure of 7-amino-2-methylsulfanyl-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxylic acid is reported in two crystal environments, viz. as the dimethylformamide (DMF) monosolvate, C(7)H(7)N(5)O(2)S·C(3)H(7)NO, (I), and as the monohydrate, C(7)H(7)N(5)O(2)S·H(2)O, (II), both at 293 (2) K. The triazolo[1,5-a]pyrimidine molecule is of interest with respect to the possible biological activity of its coordination compounds. While the DMF solvate exhibits a layered structural arrangement through N...O hydrogen-bonding interactions, the monohydrate displays a network of intermolecular O...O and N...O hydrogen bonds assisted by cocrystallized water molecules and weak π-π stacking intera…

chemistry.chemical_classificationPyrimidineMolecular StructureHydrogen bondStereochemistryCarboxylic acidStackingCarboxylic AcidsWaterDimethylformamideHydrogen BondingGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyCoordination complexchemistry.chemical_compoundCrystallographyPyrimidineschemistrytriazolo- [15-a]pyrimidineSettore CHIM/03 - Chimica Generale E InorganicaSolventsDimethylformamideMoleculeActa crystallographica. Section C, Crystal structure communications
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Antimicrobial activity of methylene blue and toluidine blue O covalently bound to a modified silicone polymer surface

2009

Methylene Blue or Toluidine Blue O were covalently bound to an activated silicone polymer by means of an amide condensation reaction. UV-visible absorption spectra confirmed that the dye was surface bound. The new polymers with covalently attached dye display significant bactericidal activity against Escherichia coli and Staphylococcus epidermidis with a 99.999% reduction in viable bacteria after four minutes exposure to a low power laser.

chemistry.chemical_classificationRMAbsorption spectroscopybiologyGeneral ChemistryPolymerPhotochemistrybiology.organism_classificationCondensation reactionmedicine.disease_causeRSchemistry.chemical_compoundchemistryCovalent bondStaphylococcus epidermidisAmidePolymer chemistryMaterials ChemistrymedicineEscherichia coliMethylene blueJournal of Materials Chemistry
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