Search results for "Ethylene"

showing 10 items of 2589 documents

ChemInform Abstract: Enantioselective Syntheses of Dopaminergic (R)- and (S)-Benzyltetrahydroisoquinolines.

2010

Optically pure (1S,R)- and (1R,S)-benzyltetrahydroisoquinolines (BTHIQs), 12a,b as the major diastereomers, were prepared by stereoselective reduction of the isoquinolinium salt possessing (R)- and (S)-phenylglycinol as the chiral auxiliary, respectively. The absolute configurations of (1S,R)-13a hydrochloride (O-debenzoylated derivative from 12a) and (1R,S)-12b diastereomers were unambiguously determined by single-crystal X-ray analysis. Reductive removal of the chiral auxiliary group, subsequent N-propylation, and cleavage of the methylenedioxy group furnished the optically active catecholamines (1S)-16a and (1R)-16b in good overall yield. We have separately prepared for the first time pa…

Chiral auxiliarychemistry.chemical_compoundchemistryHydrochlorideStereochemistryDopaminergicEnantioselective synthesisDiastereomerStereoselectivityGeneral MedicineEnantiomerMethylenedioxyChemInform
researchProduct

CCDC 724636: Experimental Crystal Structure Determination

2010

Related Article: Fei Cheng, J.M.Dyke, F.Ferrante, A.L.Hector, W.Levason, G.Reid, M.Webster, Wenjian Zhang|2010|Dalton Trans.|39|847|doi:10.1039/b911016j

Chloro-(NNN'N''N''-pentamethyldiethylenetriamine-NN'N'')-germanium(ii) trichlorogermanate(ii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

Supramolecular PEG-co-oligo(p-benzamide)s prepared on a peptide synthesizer.

2007

An automated synthesis protocol has been developed for the preparation of oligo(p-benzamide)s on solid support using a commercial peptide synthesizer employing a variation of standard Fmoc chemistry. Bis(trichloromethyl carbonate) in NMP was used to activate the aromatic carboxylic acids for acylation of secondary aromatic amines on solid support. N-Protected hepta(p-benzamide) was automatically prepared on solid support and manually converted to a solid supported block co-oligomer by attaching a poly(ethylene glycol) chain. Cleavage from the support could be achieved with minimal loss of the p-methoxybenzyl N-protective group. While the N-protected block co-oligomer was molecularly dissolv…

ChloroformMagnetic Resonance SpectroscopyProtein ConformationSupramolecular chemistryBiocompatible MaterialsGeneral ChemistryNuclear magnetic resonance spectroscopyBiochemistryTolueneCatalysisPolyethylene GlycolsGel permeation chromatographyAcylationchemistry.chemical_compoundColloid and Surface ChemistrychemistryMicroscopy Electron TransmissionModels ChemicalPolymer chemistryBenzamidesChromatography GelBenzamidePeptidesEthylene glycolJournal of the American Chemical Society
researchProduct

Responses of citrus plants to ozone: leaf biochemistry, antioxidant mechanisms and lipid peroxidation.

2006

The effects of ozone upon 3-year-old trees of Clementina mandarin (Citrus clementina Hort. ex Tan.) cv. Marisol exposed for 12 months to ambient (10 nl l(-1)) and high (30 and 65 nl l(-1)) concentrations in open top chambers (OTCs) were investigated. The data showed that in leaves, ozone reduced total chlorophylls, carotenoid and carbohydrate concentration. and increased 1-aminocyclopropane-1-carboxylic acid (ACC) content and ethylene production. In treated plants, the ascorbate leaf pool was decreased, while lipid peroxidation and Solute leakaGe were significantly higher than in ozone-free controls. The data indicated that ozone triggered protective mechanisms against oxidative stress in c…

ChlorophyllCitrusAntioxidantOzoneEthylenePhysiologymedicine.medical_treatmentAmino Acids CyclicPlant ScienceAscorbic Acidmedicine.disease_causeAntioxidantsLipid peroxidationchemistry.chemical_compoundOzoneGeneticsmedicineCarotenoidchemistry.chemical_classificationAir Pollutantsbiologyfood and beveragesEthylenesbiology.organism_classificationCarotenoidsPlant LeavesRutaceaechemistryBiochemistryChlorophyllCarbohydrate MetabolismLipid PeroxidationOxidative stressPlant physiology and biochemistry : PPB
researchProduct

Determination of antifreeze substances in the airport runoff waters by solid-phase microextraction and gas chromatography–mass spectrometry method

2016

Abstract A new method has been developed for the determination of antifreeze agents such as ethylene glycol (EG), propylene glycol (PG), and diethylene glycol (DEG) in the samples of airport runoff water. The method is based on headspace solid–phase microextraction (HS–SPME) of target analytes, which is coupled with gas chromatography–mass spectrometry (GC–MS). Until now, there was a lack of appropriate methodology for collecting reliable data about the concentration levels of these toxic de/anti-icing substances in the new type of environmental samples such as the airport runoff water. The evaluation of green extraction technique, i.e., HS–SPME resulted in establishing the optimal extracti…

Chromatography010401 analytical chemistryExtraction (chemistry)StormwaterDiethylene glycol010501 environmental sciencesMass spectrometrySolid-phase microextraction01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental chemistryAntifreezeGas chromatography–mass spectrometryEthylene glycolSpectroscopy0105 earth and related environmental sciencesMicrochemical Journal
researchProduct

High-resolution pyrolysis–gas chromatography with a movable reaction zone

1997

Abstract A new device was constructed for pyrolysis–gas chromatography and it was laboratory tested. The device enables the thermal degradation of polymers inside a capillary pre-column and transfer of the reaction zone into a column oven. The pyrolysis procedure described protects the thermally sensitive compounds prior to pyrolysis, prevents the process of irreversible condensation of high-boiling pyrolysis products during the chromatographic process and eliminates extracolumn effects on the peak broadening.

ChromatographyCapillary actionOrganic ChemistryCondensationAnalytical chemistryGeneral MedicinePolyethyleneBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundThermal degradation of polymerschemistrylawScientific methodFlame ionization detectorGas chromatographyPyrolysisJournal of Chromatography A
researchProduct

Thermal degradation of novolac resins by pyrolysis-gas chromatography with a movable reaction zone

1999

Abstract A previously described, a pyrolysis device with a movable reaction zone was used in the present work for thermal degradation of novolac resins. The products of thermal reactions were analysed by pyrolysis–GC. Owing to the heating of reaction zone to the maximal temperature of the chromatographic column, the high boiling pyrolysis products could be analysed. Bisphenols and trisphenols with aromatic rings coupled by methylene bridges and its methyl derivatives have been found among the compounds. The structure of the heavy pyrolysis products has been confirmed using GC–MS.

ChromatographyChemistryOrganic ChemistryAromaticityGeneral MedicineMass spectrometryBiochemistryAnalytical Chemistrychemistry.chemical_compoundBoilingDegradation (geology)Gas chromatographyMethylenePyrolysisElectron ionizationJournal of Chromatography A
researchProduct

Microporous hypercrosslinked polystyrene Styrosorb as a restricted access packing in sample clean-up for high performance liquid chromatography. Part…

1993

Styrosorb is a beaded microporous polystyrene with particle sizes between 2 and 4 μm. In spite of hypercrosslinkage the material was seen to swell in organic solvents. The native material is functionalized with Tris-groups at the outer surface of the particles. The average pore diameter was determined as 1.45±0.3 nm from size exclusion data using polystyrene and polyethylene standards in THF. The reversed phase behavior of the restricted access phase Styrosorb was investigated by injection of two test mixtures. Mixture I contained five aromatic amines, mixture II consisted of AmperozideR and four related compounds. The optimum range of mobile phase composition was assessed so that analytes …

ChromatographyElutionChemistryOrganic ChemistryClinical BiochemistrySize-exclusion chromatographyMicroporous materialPolyethyleneBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundPhase (matter)ParticlePolystyreneChromatographia
researchProduct

Chromium(VI) oxide oxidation of non-ethoxylated and ethoxylated alcohols for determination by electrospray ionization mass spectrometry

2010

A new derivatization procedure to increase the sensitivity of electrospray ionization mass spectrometry (ESI-MS) to non-ethoxylated and ethoxylated alcohols was investigated. The analytes were oxidized with chromium(VI) oxide and the resulting carboxylic and ethoxy-carboxylic acids were isolated by extraction with ethyl acetate; the extracts were alkalinized and infused into the ESI-MS system working in the negative-ion mode. The yields of the combined oxidation-extraction were ca. 100% for non-ethoxylated fatty alcohols dissolved in acetone and they decreased moderately in samples containing increasing amounts of water (e.g., a 75% yield was obtained with 50% water). Ethoxylated alcohols w…

ChromatographyEthylene oxideCetyl alcoholElectrospray ionizationOrganic ChemistryExtraction (chemistry)Ethyl acetateAnalytical Chemistrychemistry.chemical_compoundchemistryStearic acidDerivatizationSpectroscopyStearyl alcoholRapid Communications in Mass Spectrometry
researchProduct

Alkaline haematin D-575, a new tool for the determination of haemoglobin as an alternative to the cyanhaemiglobin method. I. description of the method

1984

A new method for the rapid and accurate measurement of haemoglobin has been developed as an alternative to the conventional cyanhaemiglobin method. This method is based on the conversion of all haeme, haemoglobin, and haemiglobin species into a stable end product by an alkaline solution of a non-ionic detergent ('AHD reagent'). The reaction product, designated as alkaline haematin D-575, is extremely stable and shows a characteristic absorption peak at 575 nm. As compared to the cyanhaemiglobin method, the determination of haemoglobin by alkaline haematin D-575 offers several advantages such as (1) extreme stability of the AHD reagent and the conversion product, (2) decreased conversion tim…

ChromatographyHemeproteinOctoxynolChemistryStereochemistrySmokingBiochemistry (medical)Clinical BiochemistryHemeGeneral MedicineHydrogen-Ion ConcentrationBiochemistryHaematinPolyethylene GlycolsReaction productPhotometryHemoglobinschemistry.chemical_compoundBasic solutionReagentHeminHumansHemoglobinClinica Chimica Acta
researchProduct