Search results for "pine"

showing 10 items of 2022 documents

Methacrylate monolithic columns functionalized with epinephrine for capillary electrochromatography applications.

2013

Epinephrine-bonded polymeric monoliths for capillary electrochromatography (CEC) were developed by nucleophilic substitution reaction of epoxide groups of poly(glycidyl-methacrylate-co-ethylenedimethacrylate) (poly(GMA-co-EDMA)) monoliths using epinephrine as nucleophilic reagent. The ring opening reaction under dynamic conditions was optimized. Successful chemical modification of the monolith surface was ascertained by in situ Raman spectroscopy characterization. In addition, the amount of epinephrine groups that was bound to the monolith surface was evaluated by oxidation of the catechol groups with Ce(IV), followed by spectrophotometric measurement of unreacted Ce(IV). About 9% of all th…

chemistry.chemical_classificationCapillary electrochromatographygeographygeography.geographical_feature_categoryChromatographyEpinephrineOrganic ChemistryEpoxideChemical modificationGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryCapillary ElectrochromatographyReagentNucleophilic substitutionSurface modificationMethacrylatesMonolithAlkylJournal of chromatography. A
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Theoretical study of the OH addition to the β-pinene

2004

The initial step of the mechanism of the OH + β-pinene gas-phase reaction was investigated by means of ab initio calculations. Four different possibilities for the OH addition to the double bond are discussed, corresponding to the addition on each C atom of the double bond, and for each one, either the syn or anti OH attack to the two methyl groups on the (bi)cyclic molecule. Energy barriers calculated at the QCISD(T)/6-31G(d) level of theory on UMP2/6-31G(d) optimised structures, show that there are preferred orientations for the OH addition under atmospheric conditions of temperature and pressure.

chemistry.chemical_classificationCrystallographyPinenechemistry.chemical_compoundTemperature and pressurechemistryDouble bondAb initio quantum chemistry methodsComputational chemistryAtomGeneral Physics and AstronomyMoleculePhysical and Theoretical ChemistryChemical Physics Letters
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Preparation and Structures of Isoindolone- or Pyrimidone-Condensed Heterocycles Containing a Hydroxy Group on a Cyclohexane or Norbornane Moiety

2009

With DL-valinol, 3-amino-1-propanol and o-aminothiophenol, aroyl(bi/tri)cyclic lactones 1 and 2 were cy- clized to isoindole- 4-6, 8, 9, pyrimidinone- 10 or thiazepine- 7 condensed heterocycles. The ketal lactone 3 furnished the benzthiazoloisoindole 9 and mixtures of epimeric hydroxyphthalazinoquinazolinones 11 and 12. The structures were es- tablished by means of 1 H and 13 C NMR spectroscopy and in some cases by X-ray crystallography.

chemistry.chemical_classificationCyclohexaneOrganic ChemistryCarbon-13 NMRBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryThiazepineMoietyPyrimidoneNorbornaneIsoindoleLactoneLetters in Organic Chemistry
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Synthesis and biological evaluation of the new ring system benzo[f]pyrimido[1,2-d][1,2,3]triazolo[1,5-a][1,4]diazepine and its cycloalkane and cycloa…

2021

Derivatives of the new ring system benzo[f]pyrimido[1,2-d][1,2,3]triazolo[1,5-a][1,4]diazepinone and its cycloalkane and cycloalkene condensed analogues have been conveniently synthesized through a three-step reaction sequence. An atom-economical, one-pot, three-step cascade process engaging five reactive centers (amide, amine, carbonyl, azide, and alkyne) has been performed for the synthesis of alicyclic derivatives of quinazolinotriazolobenzodiazepine using cyclohexane, cyclohexene, and norbornene β-amino amides. The stereochemistry and relative configurations of the synthesized compounds were determined by 1D and 2D NMR spectroscopy and X-ray crystallography. The reaction was also perfor…

chemistry.chemical_classificationGeneral Chemical EngineeringCyclohexeneAlkyneGeneral ChemistryMedicinal chemistrychemistry.chemical_compoundCycloalkaneDiazepinechemistryAmideAzideCycloalkeneNorborneneRSC Advances
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The effect of pH on polymorph formation of the pharmaceutically active compound tianeptine.

2012

The anti-depressant pharmaceutical tianeptine has been investigated to determine the dynamics of polymorph formation under various pH conditions. By varying the pH two crystalline polymorphs were isolated. The molecular and crystal structures have been determined to identify the two polymorphs. One polymorph is an amino carboxylic acid and the other polymorph is a zwitterion. In the solid state the tianeptine moieties are bonded through hydrogen bonds. The zwitterion was found to be less stable and transformed to the acid form. During this investigation an amorphous form was identified.

chemistry.chemical_classificationHydrogen bondChemistryThiazepinesCarboxylic acidPharmaceutical ScienceCrystal structureAntidepressive Agents TricyclicHydrogen-Ion Concentrationlaw.inventionAmorphous solidCrystallographychemistry.chemical_compoundX-Ray DiffractionlawActive compoundZwitterionSpectroscopy Fourier Transform InfraredmedicineTianeptineCrystallizationCrystallizationPowder Diffractionmedicine.drugInternational journal of pharmaceutics
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Activities of Two Peptidases in Resting and Germinating Seeds of Scots Pine, Pinus sylvestris

1975

Extracts prepared from resting seeds of Scots pine, Pinus sylvestris L., rapidly hydrolysed two peptides, Leu–Tyr and Ala–Gly, at pH 8.6 and 7.8, respectively. In gel chromatography on Sephadex G-100 the two activities were eluted as separate peaks, which indicates that they are due to two different peptidases. The seeds were allowed to germinate at 20°C, the activities of the two enzymes were assayed separately on extracts from the endosperm and seedling tissues at different stages of germination, and compared with corresponding changes in dry weight and total nitrogen. Both enzyme activities were relatively high in the endosperm of resting seeds, and they increased about 2- and 3-fold dur…

chemistry.chemical_classificationHydrolyzed proteinbiologyPhysiologyScots pinefood and beveragesCell BiologyPlant ScienceGeneral Medicinebiology.organism_classificationEndospermEnzymeDry weightchemistryGerminationSephadexSeedlingBotanyGeneticsPhysiologia Plantarum
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First reactions of dialkoxycarbenium tetrafluoroborates with pyrroles, 5H-dibenz[b,f]azepines, and electron-rich arenes

2009

Pyrrole (2a) and 2,5-dimethylpyrrole (2b) react with the dialkoxycarbenium tetrafluoroborates 1a-1c under kinetic control to yield the corresponding acylpyrrole derivatives. 5H-Dibenz[b,f]azepine (9a) and the 10,11-dihydro derivative 9b react only with the most electrophilic of the series of electrophiles tested, namely, diethoxycarbenium tetrafluoroborate (1a), to furnish the corresponding formyl derivatives. Similarly, in arene chemistry, the highly electron-rich N,N-dimethylaniline (13a) and 1,3,5-trimethoxybenzene (13b) are formylated by reaction with 1a.

chemistry.chemical_classificationKetoneTetrafluoroborateTertiary amineOrganic ChemistryRegioselectivityMedicinal chemistryFormylationchemistry.chemical_compoundchemistryElectrophileOrganic chemistryAzepinePyrroleJournal of Heterocyclic Chemistry
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Fast and continuous synthesis of nanostructured iron spinel in supercritical water: influence of cations and citrates

2014

International audience; Spinel iron oxide nanoparticles were obtained under supercritical water conditions in a continuous and fast (less than 10s) way by modifying the initial stoichiometric Fe II /Fe III molar ratio from (1/2) to (3/0), without base solution, and using citrates directly with iron precursors. This result opens the way of an economical and environmentally benign approach to synthesize superparamagnetic iron oxide nanoparticles (SPIONs) in important yields.

chemistry.chemical_classificationMaterials scienceBase (chemistry)Superparamagnetic iron oxide nanoparticlesGeneral Chemical EngineeringSpinelInorganic chemistry02 engineering and technologyGeneral Chemistryengineering.material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences7. Clean energySupercritical fluid0104 chemical scienceschemistry.chemical_compoundchemistryMolar ratioengineeringIron oxide cycle[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics0210 nano-technologyStoichiometryIron oxide nanoparticles
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Tyramine action on motoneuron excitability and adaptable tyramine/octopamine ratios adjust Drosophila locomotion to nutritional state

2019

Adrenergic signaling profoundly modulates animal behavior. For example, the invertebrate counterpart of norepinephrine, octopamine, and its biological precursor and functional antagonist, tyramine, adjust motor behavior to different nutritional states. In Drosophila larvae, food deprivation increases locomotor speed via octopamine-mediated structural plasticity of neuromuscular synapses, whereas tyramine reduces locomotor speed, but the underlying cellular and molecular mechanisms remain unknown. We show that tyramine is released into the CNS to reduce motoneuron intrinsic excitability and responses to excitatory cholinergic input, both by tyraminehonoka receptor activation and by downstrea…

chemistry.chemical_classificationMultidisciplinaryCalcium channelTyramineNorepinephrinechemistry.chemical_compoundmedicine.anatomical_structurechemistryNeuromodulationBiogenic aminemedicineExcitatory postsynaptic potentialCholinergicOctopamine (neurotransmitter)Neurosciencemedicine.drugProceedings of the National Academy of Sciences
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Studies on the synthesis of heterocyclic compounds. Part VIII. A facile synthesis of new pyrazolo[3,4-b]benzazepine-4,9-diones

1982

2-Carbomethoxybenzoyl chloride reacted with some 5-methylamino-l-phenyl-3-R-pyrazoles to yield N-methyl-l-phenyl-3-R-pyrazol-5-yl)-2-carbomethoxybenzamides. These products were readily transformed into the corresponding acid, which in turn, refluxed in phosphorus oxychloride afforded the tricyclic system, l-phenyl-3-R-pyrazolo[3,4-b]benzazepine-4,9-dione.

chemistry.chemical_classificationPhosphorusOrganic Chemistrychemistry.chemical_elementChlorideBenzazepineTurn (biochemistry)chemistry.chemical_compoundchemistryYield (chemistry)medicineOrganic chemistrymedicine.drugTricyclicJournal of Heterocyclic Chemistry
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