Search results for "Aliphatic compound"

showing 10 items of 53 documents

Anthelminthika, III Synthese und 13C-NMR-spektroskopische eigenschaften von (fluor- und iodanilino)ethentricarbonitrilen)

1987

Zusammenfassung Die Umsetzung von Ethentetracarbonitril mit entsprechenden Halogenanilinen fuhrt zu Anilinoethentricarbonitrilen mit den folgenden Halogensubstitutionen: 2-Fluor-, 3-Fluor-, 4-Fluor-, 2,4-Difluor-, 3-Iod- und 4-Iod. Die dargestellten (Fluor- und Iodanilino)ethentricarbonitrile vermogen insbesondere anthelminthische, fungizide und herbizide Wirkungen auszuuben. Die Struktur der Endprodukte wird durch die IR-, 1 H-NMR-, 13 C-NMR- und Massenspektren charakterisiert.

Inorganic Chemistrychemistry.chemical_compoundNitrileChemistryOrganic ChemistryEnvironmental ChemistryAmine gas treatingNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryAliphatic compoundBiochemistryMedicinal chemistryJournal of Fluorine Chemistry
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Mass spectra of halogenated esters 5—Chloromethyl esters of aliphatic C2C12n-carboxylic acids and their monochlorinated derivatives

1984

A study has been made of the mass spectral fragmentation upon electron impact of aliphatic C2C12 chloromethyl esters and all their 66 monochlorinated derivatives. The fragmentation pathways of the parent chloromethyl esters were elucidated with the aid of the 1st FFR metastable ions. A McLafferty rearrangement gives the base peak in the C6C11 parent esters and in almost all the 4-chloro and ω-chloro isomers. The subsequent loss of HCl gives a very characteristic peak of the chloromethyl esters and their (3-ω)-chloro derivatives at m/z 72, [C3H4O2]+. The 2-chloro isomers have the corresponding chlorine-containing fragment ion at m/z 106/108. The mass spectra of 2-, 3-, 4-, 5- and ω-chloro is…

McLafferty rearrangementFragmentation (mass spectrometry)ChemistryMass spectrumMolecular MedicineOrganic chemistryAliphatic compoundInstrumentationBiochemistryMedicinal chemistrySpectroscopyElectron ionizationIonOrganic Mass Spectrometry
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Mass spectra of halogenated esters. 7. Methyl esters of 2-chloro C2C20n-alkanoic acids

1988

The mass spectral fragmentation of a homologous series of methyl esters of 2-chloro n-alkanoic acids ranging from acetic (C2) to eicosanoic (C20) acid on electron impact has been investigated. The fragmentation pathways were elucidated with the aid of the first field-free region metastable ions, the results being presented with one compound, i.e. with ionized methyl 2-chloro-octauoate. Owing to the Cl/H exchanges and to the formation of the non-chlorinated parent esters prior to the fragmentations the spectra show the peak pairs with and without the chlorine atom. The effects become more evident with increasing chain length; shown most visually by the abundance ratios of the McLafferty rear…

McLafferty rearrangementStereochemistryBiochemistryMedicinal chemistryIonHomologous serieschemistry.chemical_compoundchemistryFragmentation (mass spectrometry)IonizationMass spectrumMolecular MedicineAliphatic compoundInstrumentationSpectroscopyElectron ionizationOrganic Mass Spectrometry
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Self-Sorting Dimerization of Tetraurea Calix[4]arenes

2007

Calix[4]arenes substituted by four urea functions are self-complementary molecules that spontaneously combine in apolar solvents in the presence of an ammonium salt to form dimeric capsules held together by a belt of hydrogen bonds. In the presence of tetraethylammonium salts, the Et4N+ cation is included as a guest. The sorting between dimeric capsules formed in a mixture of calix[4]arenes directly depends on the steric crowding of the substituents grafted on the urea groups whether aromatic derivatives or aliphatic chains linking urea functions in mono-, di-, or tetraloop structures. Simple rules allow one to anticipate which capsules will be exclusively formed when calix[4]arenes are mix…

Models MolecularSteric effectsMagnetic Resonance SpectroscopyMolecular StructureHydrogen bondStereochemistryDimerOrganic ChemistryStereoisomerismNuclear magnetic resonance spectroscopyInclusion compoundchemistry.chemical_compoundPhenolschemistryPolymer chemistryCalixareneUreaMoleculeCalixarenesAliphatic compoundDimerizationThe Journal of Organic Chemistry
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Synthesis of (±)-(E)-2,6-dimethyl-6-hydroxyocta-2,7-dienoic acid and the corresponding amide (“acacialactam”)

1994

Abstract The total synthesis of the title compounds in racemic form is described. Linalool was used as the starting material and transformed into the target molecules in 6 steps. The synthetic amide displays spectral properties identical to those reported for the natural compound acacialactam, indicating that the structure proposed for the latter compound is not correct.

OzonolysisOrganic ChemistrySpectral propertiesTotal synthesisBiochemistrychemistry.chemical_compoundLinaloolchemistryAmideDrug DiscoveryWittig reactionMoleculeOrganic chemistryAliphatic compoundTetrahedron Letters
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Photochemistry of Fluorinated Heterocyclic Compounds. An Expedient Route for the Synthesis of Fluorinated 1,3,4-Oxadiazoles and 1,2,4-Triazoles

2004

The photochemistry of some 3-N-alkylamino-5-perfluoroalkyl-1,2,4-oxadiazoles in the presence of nitrogen nucleophiles such as ammonia and primary and secondary aliphatic amines has been investigated. The primary photolytic intermediate from the cleavage of the ring O-N bond follows two distinct and competing pathways leading to (i). 5-perfluoroalkyl-1,3,4-oxadiazoles, through the ring contraction-ring expansion photoisomerization route favored by the presence of the base or (ii). 5-perfluoroalkyl-1,2,4-triazoles, through the intervention, as an internal nucleophile, of the exocyclic N-alkylamino moiety of the oxadiazole followed by the attack of the external nitrogen nucleophile and subsequ…

RING-PHOTOISOMERIZATIONPrimary (chemistry)PhotoisomerizationFLUORO HETEROCYCLESChemistryOrganic ChemistryOxadiazoleContext (language use)Settore CHIM/06 - Chimica OrganicaRing (chemistry)Photochemistrychemistry.chemical_compoundNucleophile124-OXADIAZOLE DERIVATIVESMoiety5-MEMBERED HETEROCYCLESAliphatic compoundPHOTOINDUCED MOLECULAR-REARRANGEMENTSThe Journal of Organic Chemistry
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Electroreduction of aliphatic chlorides at silver cathodes in water

2010

The effect of water on the reduction of aliphatic chlorides at silver cathodes was investigated by cyclovoltammetric experiments in acetonitrile, water and their mixture and focused electrolyses in water solutions. The addition of water to acetonitrile gives rise to the formation of new peaks and/or the displacement of pre-existent peaks at dramatically less negative potentials. In a water medium, silver shows a very large electrocatalytic effect towards the reduction of chlorinated aliphatic compounds belonging to the classes of chloromethanes, chloroethanes and chloroethenes, dramatically higher than that observed in aprotic solvents such as dimethylformamide (DMF) or acetonitrile (ACN). …

Reaction mechanismSilverAqueous solutionChemistryGeneral Chemical EngineeringElectrocatalysiInorganic chemistryDe-halogenationSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryElectrocatalystAnalytical Chemistrychemistry.chemical_compoundElectrochemistryDimethylformamideWater treatmentElectrochemical remediationAliphatic compoundAcetonitrileAliphatic chlorideJournal of Electroanalytical Chemistry
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Catalytic aminomercuration of olefins in a tandem aminomercuration-deoxymercuration; One-step synthesis of secondary n-arylallylamines from allylalco…

1990

Abstract Allyl alcohols react with primary aromatic amines and stoichiometric amounts of mercury(II) tetrafluoroborate to give mixtures of mono- and diallyl anilines. However, the use of the tandem aminomercuration-deoxymercuration promoted by catalytic mercury(II) tetrafluoroborate allows to perform regiospecifically the monoallylation reaction with very high yields. A mechanism is proposed to account for the observed results.

Reaction mechanismTetrafluoroborateOrganic ChemistryBiochemistryCatalysisAdductchemistry.chemical_compoundAnilinechemistryDrug DiscoveryOrganic chemistryAmine gas treatingAliphatic compoundAminationTetrahedron
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Synthesis of optically pure alkynols

1993

Abstract (R,S)-1-alkylprop-2-yn-1-ols have been separated by a 2-step procedure, esterification with N-p-tosyl-(L)-phenylalanine (or valine), recrystallisation of the diastereomeric esters from ethanol/hexane and saponification of the optically pure esters.

Recrystallization (geology)EthanolOrganic ChemistryDiastereomerCatalysisInorganic ChemistryHexanechemistry.chemical_compoundchemistryValineOrganic chemistryPhysical and Theoretical ChemistryAliphatic compoundSaponificationTetrahedron: Asymmetry
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Distribution of Volatile Organic Compounds in Sicilian groundwaters analysed by Head Space Solid Phase Micro Extraction coupled with Gas Chromatograp…

2008

This work presents the results of an assessment of the existence and concentration of 13 volatile organic compounds (VOCs) in groundwaters from 14 hydrological basins in Sicily (25,710 km2). On the basis of hydrological, hydrogeochemical and geological studies, 324 sampling points were selected. All groundwater sampled were collected twice, from October to December 2004 and from February to May 2005, and were analysed to determine the concentration and spatial distribution of the VOCs in the aquifers. The need to analyze a large number of samples in a short space of time so as to obtain quantitative analyses in trace concentration levels spurred us to create a new analytical method, both si…

Settore CHIM/10 - Chimica Degli AlimentiGroundwater pollution SPME VOCs Sicily Sum chlorinated aliphatic compounds Groundwater monitoring
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