Search results for "Benzaldehyde"

showing 10 items of 112 documents

Zur verzögernden wirkung aromatischer aldehyde auf die radikalische polymerisation von vinylverbindungen

1972

Die Einwirkung einer Reihe aromatischer Aldehyde auf die mit α.α-′Azobisisobuttersaurenitril gestarteten Polymerisationen von Styrol und Methacrylsauremethylester wurde untersucht (a) durch Vergleich der Polymerausbeuten; (b) durch quantitative Analyse der UV-Spektren der gereinigten Polymeren und (c) durch Vergleich ihrer Mn- und Mn-Werte. Bei der Styrolpolymerisation zeigen 4-Phenyl-benzaldehyd und Indol-3-aldehyd keine Einwirkung. 4-Phenylazo-benzaldehyd, Benzaldehyd, Anthracen-9-aldehyd und m-(2.4-Dinitrophenoxy)-benzaldehyd verzogern die Polymerisation. Bis auf Benzaldehyd wird hierbei ihr kovalenter Einbau in das Polystyrol nachgewiesen. Fur 4-Phenylazo-benzaldehyd konnte eine scheinb…

chemistry.chemical_classificationBenzaldehydechemistry.chemical_compoundchemistryPolymerizationPolymer chemistryPolymerPolystyreneMethyl methacrylateAldehydeStyreneDie Makromolekulare Chemie
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4-(2-Adamantyl)thiosemicarbazone

1984

Aus der Umsetzung von 4-(2-Adamantyl)thiosemicarbazid (1) mit den Carbonylverbindungen 2a-d gehen die 4-(2-Adamantyl)thiosemicarbazone 3a-d hervor. Die Startkomponente 1 ist aus 2-Aminoadamantan (4) uber das (2-Adamantyl)-isothiocyanat (5) zuganglich. Verbindung 5 und Vertreter des Strukturtyps 3 vermogen antivirale, antimykotische und antipyretische Wirkung auszuuben. Antiviral Agents, XXIV: 4-(2-Adamantyl)thiosemicarbazones Reactions of 4-(2-adamantyl)thiosemicarbazide (1) with the carbonyl compounds 2a-d yield the 4-(2-adamantyl)thiosemicarbazones 3a-d. The starting material 1 is accessible from 2-aminoadamantane (4) via 2-adamantyl isothiocyanate (5). Compound 5 and representatives of t…

chemistry.chemical_classificationBenzaldehydechemistry.chemical_compoundchemistryStereochemistryAdamantaneDrug DiscoveryIsothiocyanatePharmaceutical ScienceStructure typeSemicarbazoneAldehydeArchiv der Pharmazie
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Model studies on a diastereoselective synthesis of the C(33)–C(37) fragment of Amphotericin B

2003

Abstract A new, short and highly diastereoselective synthetic route aiming at the C(33)–C(37) fragment of Amphotericin B has been developed. Studies with a model aldehyde (benzaldehyde) have given very promising results: the desired stereochemistry of all four stereocenters of the target molecule has been achieved with high diastereoselection. The stereochemistry of three key intermediates and the target segment has been confirmed by X-ray crystallography.

chemistry.chemical_classificationChemistryStereochemistryFragment (computer graphics)Organic ChemistryEnantioselective synthesisBiochemistryAldehydeStereocenterBenzaldehydechemistry.chemical_compoundAldol reactionAmphotericin BDrug DiscoverymedicineMoleculemedicine.drugTetrahedron
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Catalytic condensation of aromatic aldehydes with acetone on activated Mg-Al mixed oxides

2004

Abstract The factors affecting the aldol condensation of some model aromatic aldehydes (benzaldehyde, the three isomers of F-benzaldehyde and 2-naphthaldeyde) with acetone have been investigated using heterogeneous catalysts obtained by the calcination of hydrotalcite-type (HT) precursors at 773 K for 8 h, followed by rehydration at room temperature for 7 h under a flow of N 2 saturated with water vapour. At 273 K the main product was the β-hydroxy-ketone, while at 318 K it mainly dehydrated to the corresponding trans -arylideneacetone, with small amounts ( cis -arylideneacetone, 1,3-diarylideneacetone and 4-hydroxy-4-methyl-2-pentanone. High reaction times favoured the formation of trans -…

chemistry.chemical_classificationHydrotalciteProcess Chemistry and TechnologyInorganic chemistryGeneral ChemistryAldehydeCatalysislaw.inventionCatalysisBenzaldehydechemistry.chemical_compoundchemistrylawAcetoneCalcinationAldol condensationAtomic ratioNuclear chemistry
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Electrochemical carboxylation of aldehydes and ketones with sacrificial aluminum anodes.

1986

Abstract The electrocarboxylation of aldehydes to the corresponding α-hydroxyacids was described as impossible with conventional electrochemical systems. It is reported here that it is possible to realize it in diaphragmless cells making of sacrificial aluminum anodes. The method can be used also for the electrocarboxylation of ketones with good yields.

chemistry.chemical_classificationKetoneOrganic ChemistryInorganic chemistryElectrochemistryBiochemistryAldehydeAnodeBenzaldehydechemistry.chemical_compoundchemistryCarboxylationDrug DiscoveryElectrodeAcetophenoneTetrahedron Letters
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Photoelectrocatalytic selective oxidation of 4-methoxybenzyl alcohol in water by TiO2 supported on titanium anodes

2013

The photoelectrocatalytic partial oxidation of 4-methoxybenzyl alcohol in aqueous solution irradiated by near-UV light was carried out in a three-electrode batch reactor. TiO2 films were either deposited by dip-coating of a TiO2 sol onto a Ti foil and subsequent calcination or generated on Ti plates by thermal oxidation in air at 400-700 degrees C. The effects of the anode preparation method and bias potential values on conversion and selectivity to the corresponding aldehyde were investigated. The photoelectrocatalytic results were compared with the photocatalytic and electrocatalytic ones. The results indicated that no reaction occurred during the electrocatalytic experiments, whereas the…

chemistry.chemical_classificationPhotoelectrocatalysis Titanium TiO2/Ti 4-Methoxybenzaldehyde Aromatic alcohols Green synthesisProcess Chemistry and TechnologyInorganic chemistryAlcoholAldehydeCatalysislaw.inventionchemistry.chemical_compoundchemistrylawBenzyl alcoholSaturated calomel electrodePhotocatalysisCalcinationReactivity (chemistry)Partial oxidationGeneral Environmental Science
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Polymeric nitrones, 1. Synthesis and modification of polymeric nitrones derived from polymerizable aldehydes

1999

The model compound N,C-diphenylnitrone[N-(benzylidene)aniline-N-oxide] (3) was prepared by condensation of benzaldehyde with phenylhydroxylamine to study its thermal stability. X-ray diffraction analysis of a single crystal established the conformation of the nitrone group. A new monomer 4-(methacryloyloxy)benzaldehyde-phenylnitrone (8) was also prepared and could not be polymerized with 2,2′-azobisisobutyronitrile (AIBN) as initiator at 70°C. Under these conditions the nitrone reacted exclusively in an intermolecular 1,3-dipolar cycloaddition to give oligomeric tetrahydro-1,2-oxazoline derivates. The kinetics of the cycloaddition was investigated. Additionally, different (meth)acryl- and s…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationCondensed Matter PhysicsCondensation reactionAldehydeCycloadditionNitroneBenzaldehydechemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryPhenylhydroxylamineMacromolecular Chemistry and Physics
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Phosphido- and Amidozirconocene Cation-Based Frustrated Lewis Pair Chemistry

2015

Methyl abstraction from neutral [Cp2ZrMe(ERR')] complexes 1 (E = N, P; R, R' = alkyl, aryl) with either B(C6F5)3 or [Ph3C][B(C6F5)4] results in the formation of [Cp2Zr(ERR')][X] complexes 2 (X(-) = MeB(C6F5)3(-), B(C6F5)4(-)). The X-ray structure of amido complexes [Cp2Zr(NPh2)][MeB(C6F5)3] (2d) and [Cp2Zr(N(t)BuAr)][B(C6F5)4] (2e', Ar = 3,5-C6H3(CH3)2) is reported, showing a sterically dependent Zr/N-π interaction. Complexes 2 catalyze the hydrogenation of electron-rich olefins and alkynes under mild conditions (room temperature, 1.5 bar H2). Complex 2e binds CO2, giving [Cp2Zr(CO2)(N(t)BuAr)]2[MeB(C6F5)3]2 (3e). Amido complex 2d reacts with benzaldehyde yielding [Cp2Zr(OCH2Ph)((OC)PhNPh2)…

chemistry.chemical_classificationSteric effectsStereochemistryArylGeneral ChemistryBiochemistryMedicinal chemistryCatalysisFrustrated Lewis pairBenzaldehydechemistry.chemical_compoundColloid and Surface ChemistrychemistryDiphenylacetyleneAlkylJournal of the American Chemical Society
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Identification of the Iodination and Bromination Products of 3-Hydroxybenzaldehyde: Preparation of 5-Hydroxy-2-iodobenzaldehyde

2017

The monohalogenation products of 3-hydroxybenzaldehyde (1) are useful synthons for the preparation of more complex molecules.1–4 For example, the introduction of a halogen allows the use of a Suzuk...

chemistry.chemical_compound010405 organic chemistryChemistryOrganic ChemistryHalogenSynthonHalogenationOrganic chemistry3-Hydroxybenzaldehyde010402 general chemistry01 natural sciences0104 chemical sciencesOrganic Preparations and Procedures International
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The role of H2O in the photocatalytic oxidation of toluene in vapour phase on anatase TiO2 catalyst

1999

Abstract Photocatalytic oxidation of toluene has been carried out in a gas–solid regime by using polycrystalline anatase TiO2 in a fixed-bed continuous reactor. Air containing toluene and water vapours in various molar ratios was fed to the photoreactor irradiated by a medium pressure Hg lamp. Toluene was mainly photo-oxidised to benzaldehyde, and small amount of benzene, benzyl alcohol and traces of benzoic acid and phenol were also detected. In the presence of water, no decrease of photoreactivity was observed at steady-state conditions. By removing water vapour from the feed, the conversion of toluene to benzaldehyde was almost completely inhibited, and an irreversible deactivation of th…

inorganic chemicalsInorganic chemistryGeneral ChemistryHeterogeneous catalysisPhotochemistryTolueneCatalysisCatalysisBenzaldehydechemistry.chemical_compoundchemistryBenzyl alcoholPhotocatalysisBenzeneBenzoic acidCatalysis Today
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