Search results for "Isocyanate"

showing 10 items of 47 documents

Carbon monoxide activation by a molecular aluminium imide: C-O bond cleavage and C-C bond formation

2020

Anionic molecular imide complexes of aluminium are accessible via a rational synthetic approach involving the reactions of organo azides with a potassium aluminyl reagent. In the case of K2 [(NON)Al(NDipp)]2 (NON=4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethyl-xanthene; Dipp=2,6-diisopropylphenyl) structural characterization by X-ray crystallography reveals a short Al-N distance, which is thought primarily to be due to the low coordinate nature of the nitrogen centre. The Al-N unit is highly polar, and capable of the activation of relatively inert chemical bonds, such as those found in dihydrogen and carbon monoxide. In the case of CO, uptake of two molecules of the substrate…

010405 organic chemistrySubstrate (chemistry)General Chemistry010402 general chemistry01 natural sciencesIsocyanateCatalysis3. Good health0104 chemical scienceschemistry.chemical_compoundchemistryChemical bondReagentPolymer chemistryMoleculeImideBond cleavageCarbon monoxide
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HC-SCR of NOx over Ag/alumina: a combination of heterogeneous and homogeneous radical reactions?

2005

Matrix isolation combined with EPR and FT-IR technique at low temperature has been used to study the gas phase species involved in HC-SCR over a highly active Ag/alumina catalyst. A combination of heterogeneous and homogeneous (radical) reactions is proposed to take place over a Ag/alumina catalyst during HC-SCR. Radicals of low molecular weight were trapped in a growing argon matrix behind the Ag/alumina catalyst. In the same matrix, cyanogen isocyanate was detected and is suggested to be a key intermediate for the formation of amines and ammonia via the hydrolysis of isocyanate species.

ChemistryCyanogenRadicalCatalyst supportInorganic chemistryMatrix isolationGeneral ChemistryHeterogeneous catalysisIsocyanateCatalysisCatalysischemistry.chemical_compoundOrganic chemistryNOxCatalysis Today
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Synthese von 2-Acyloxy- und 2-Alkyloxy-3-ketoglycalen und ihren Bromaddukten

1983

Die an den Hydroxygruppen acetyl-, pivaloyl- und methylgeschutzten 2-Hydroxy-3-ketoglycale 5a, 5b bzw. 11 werden durch Oxidation der entsprechenden 1-O-Acylglucopyranosen 3a, 3b bzw. 9 an der freien 3-Hydroxygruppe mit Dimethylsulfoxid/Acetanhydrid oder Chlorsulfonylisocyanat hergestellt und charakterisiert. Nur beim Acetylderivat 3a verlaufen die Oxidation und die Eliminierung des 1-Acetyloxysubstituenten in einem Schritt. Beim Pivaloylderivat 3b und beim Methylderivat 9 mus die Eliminierung aus der 3-Ulose 4 bzw. 10 mit Diazabicycloundecen (DBU) vervollstandigt werden. – Die geschutzten Hex-1-enopyran-3-ulosen 5a, 5b und 11 addieren Brom stereoselektiv unter Bildung der D-ribo-konfigurier…

Chlorosulfonyl isocyanateAnomerBromineDimethyl sulfoxideStereochemistryOrganic ChemistrySubstituentchemistry.chemical_elementAdductchemistry.chemical_compoundAcetic anhydridechemistryAcetyl derivativePhysical and Theoretical ChemistryLiebigs Annalen der Chemie
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Diversity-Oriented Synthesis of Highly Functionalized Alicycles across Dipolar Cycloaddition/Metathesis Reaction

2021

AbstractThis Account gives an insight into the selective functionalization of some readily available commercial cyclodienes across simple chemical transformations into functionalized small-molecular scaffolds. The syntheses involved selective cycloadditions, followed by ring-opening metathesis (ROM) of the resulting azetidin-2-one derivatives or isoxazoline frameworks and selective cross metathesis (CM) by discrimination of the C=C bonds on the alkenylated heterocycles. The CM protocols have been described when investigated under various conditions with the purpose on exploring chemodifferentiation of the olefin bonds and a study on the access of the corresponding functionalized β-lactam or…

Chlorosulfonyl isocyanateOlefin fiberNitrile010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryOrganofluorine chemistryMetathesis01 natural sciencesCombinatorial chemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundSalt metathesis reactionCycloalkeneSynlett
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Regio- and stereoselective synthesis of the enantiomers of monoterpene-based β-amino acid derivatives

2007

Abstract The regio- and stereospecific addition of chlorosulfonyl isocyanate to cis-δ-pinene enantiomers has furnished monoterpene-fused β-lactams. The observed regioselectivity can be explained by ab initio DFT modeling of transition state structures. In contrast with the less reactive α-pinane-fused β-lactam 4, the resulting β-lactams 5 and 13 containing an amino group connected to a secondary carbon possess similar reactivity to the cycloalkane-fused analogues and can be easily converted to the β-amino acid and its protected derivatives. The base-catalyzed isomerization of the cis-amino ester afforded the corresponding trans-amino ester in moderate yield.

Chlorosulfonyl isocyanatechemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryRegioselectivityCatalysisAmino acidInorganic Chemistrychemistry.chemical_compoundStereospecificityReactivity (chemistry)StereoselectivityPhysical and Theoretical ChemistryEnantiomerIsomerizationTetrahedron: Asymmetry
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Enantiomer separation by chiral-phase liquid chromatography of urethane derivatives of natural diacylglycerols previously fractionated by reversed-ph…

1991

Abstract Enantiomers of diacylglycerols such as 3,5-dinitrophenyl isocyanate (urethane) derivatives previously fractionated by reversed-phase high-performance liquid chromatography (HPLC) were separated by HPLC on a chiral phase column [N-( R )-1-(α-naphthyl)ethylamino-carbonyl-( S )-valine chemically bound to γ-aminopropylsilanized silica]. In addition to the separation of commercial monoacid-diacylglycerol isomers, separation of diacid-diacylglycerol isomers obtained from peanut oil and cottonseed oil triacylglycerols by chemical hydrolysis is reported. Hexane-ethylene dichloride-ethanol mixtures were used for elution of the diacylglycerol derivative isomers, which were detected by their …

Degree of unsaturationChromatographyChemistryElutionOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryIsocyanateHigh-performance liquid chromatographyAnalytical ChemistryHydrolysischemistry.chemical_compoundOrganic chemistryRacemic mixtureEnantiomerJournal of Chromatography A
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Reactions of Aminobis(phenolate)‐Supported Dioxidotungsten(VI) and Dioxidomolybdenum(VI) Complexes

2006

The dioxidotungsten(VI) and -molybdenum(VI) complexes [WO2(O2NOMe)] (1), [MoO2(O2NOMe)] (2) and [{MoO2(O2NMe)}2] (3) [O2NOMe methoxyethylamino-N,N-bis(2-methylene-4,6-dimethylphenolate) dianion, O2NMe = methylamino-N,N-bis(2-methylene-4,6-dimethylphenolate) dianion] can react with chloride sources (Me3SiCl, SOCl2) to form resultant monooxido dichloro compounds [WOCl2(O2NOMe)] (4), [MoOCl2(O2NOMe)] (5) and [MoOCl2(O2NMe)] (6), respectively. The reaction of tungsten complex yields of the mixture of cis-4 and trans-4, which can be separated and characterized. The reactions of analogous molybdenum complexes with Me3SiCl yield trans isomers of 5 and 6 as individual products. Reaction of dioxidot…

DenticityChemistryLigandchemistry.chemical_elementChlorideIsocyanateMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMolybdenumYield (chemistry)medicineOrganic chemistryIsopropylCis–trans isomerismmedicine.drugEuropean Journal of Inorganic Chemistry
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Zum metabolismus von dialkyldithiocarbamaten

1974

Abstract Metabolism dialkyldithiocarbamates. I. Determination of amines using a reaction with isocyanates followed by gas chromatographic identification of the urea derivatives formed. N,N′-Di- and N,N′,N′-trisubstituted areas, formed by the reaction of amines with isocyanates, e.g. tert. -butyl isocyanate or 3-trifluoromethylphenyl isocyanate, are useful derivatives for the gas chromatographic analysis of primary and secondary amines. The separation is carried out at temperatures between 70 and 130° on liquid phases such as silicone OV-101 and silicone OV-17. With nitrogen and electron capture detectors the detection limit is 10 10 g. Trace analysis of simple primary and secondary amines i…

Detection limitchemistry.chemical_classificationPrimary (chemistry)Organic Chemistrychemistry.chemical_elementGeneral MedicineMetabolismBiochemistryNitrogenIsocyanateAnalytical Chemistrychemistry.chemical_compoundSiliconechemistryUreaOrganic chemistryDithiocarbamateJournal of Chromatography A
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Catalytic Asymmetric Formal [3+2] Cycloaddition of 2-Isocyanatomalonate Esters and Unsaturated Imines: Synthesis of Highly Substituted Chiral γ-Lacta…

2017

[EN] Unlike their isocyano and isothiocyanato analogues, isocyanato esters remain almost unexplored as formal 1,3-dipoles in asymmetric catalytic reactions. The first asymmetric formal [3+2] cycloaddition involving isocyanato esters and electrophilic alkenes is reported. Diisopropyl 2-isocyanatomalonate reacts with a,b-unsaturated N-(o-anisidyl) imines in the presence of a Mg(OTf)2¿BOX complex to give highly substituted chiral pyrrolidinones featuring a conjugate exocyclic double bond with excellent yields and enantiomeric excesses up to 99%. Several transformations of the resulting heterocycles, including the synthesis of a pyroglutamic acid derivative, have been carried out.

Double bondLactamsStereochemistryMolecular ConformationStereoisomerismEnantioselectivityAlkenes010402 general chemistryCrystallography X-Ray01 natural sciencesCatalysisCatàlisiCoordination ComplexesAsymmetric catalysisMagnesiumPyrrolidinoneschemistry.chemical_classificationNucleophilic additionCycloaddition Reaction010405 organic chemistryNitrogen heterocyclesOrganic ChemistryEnantioselective synthesisEstersStereoisomerismGeneral ChemistryCycloadditionMalonates0104 chemical scienceschemistryFISICA APLICADAElectrophileIminesEnantiomerNucleophilic additionQuímica orgànicaIsocyanatesChemistry (Weinheim an der Bergstrasse, Germany)
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Environmental Isocyanate-Induced Asthma: Morphologic and Pathogenetic Aspects of an Increasing Occupational Disease

2011

Occupational diseases affect more and more people every year. According to the International Labour Organization (ILO), in 2000 an estimated amount of at least 160 million people became ill as a result of occupational-related hazards or injuries. Globally, occupational deaths, diseases and injuries account for an estimated loss of 4% of the Gross Domestic Product. Important substances that are related to occupational diseases are isocyanates and their products. These substances, which are used in a lot of different industrial processes, are not only toxic and irritant, but also allergenic. Although the exposure to higher concentrations could be monitored and restricted by technical means, v…

Early signsHealth Toxicology and MutagenesisOccupational diseaselcsh:MedicineDiseaseReviewAir Pollutants OccupationalIsocyanate induced asthmaToxicologyRisk groupsEnvironmental healthOccupational ExposuremedicineGenetic predispositionHumansGenetic Predisposition to Diseasepathological findingsAsthma OccupationalVolume concentrationbusiness.industrylcsh:RPublic Health Environmental and Occupational Healthclinical findingsAllergensmedicine.diseaseoccupational diseaseisocyanatebusinessoccupational asthmaOccupational asthmagenetic predispositionIsocyanatesInternational Journal of Environmental Research and Public Health
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