Search results for "romi"

showing 10 items of 2291 documents

Regioselective Synthesis of 2-Imino-1,3-thiazolidin-4-ones by Treatment ofN-(Anthracen-9-yl)-N′-ethylthiourea with Bromoacetic Acid Derivatives

2002

The reaction between N-(anthracen-9-yl)-N′-ethylthiourea (1) and methyl bromoacetate yielded mainly 2-[(anthracen-9-yl)imino]-3-ethyl-1,3-thiazolidin-4-one (2), together with some of the regioisomeric 3-(anthracen-9-yl)-2-ethylimino-1,3-thiazolidin-4-one (3). The structures of the products were elucidated by NMR techniques and, for 3, X-ray crystallographic analysis. Treatment of 1 with bromoacetyl bromide again yielded 2 and 3, but with a reversed product distribution ratio, thus providing an interesting and unexpected regioselectivity, depending on the electrophile selected. The underlying cause of the observed regioselectivity is a result of different reaction pathways taken by the two e…

chemistry.chemical_compoundN-ethylthioureachemistryBromoacetic acidBromideStereochemistryOrganic ChemistryElectrophileRegioselectivityNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryProduct distributionEuropean Journal of Organic Chemistry
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Multi-Arm 1,2,3-Thiadiazole Systems

1997

Benzene derivatives 2a–c with 6, 4, and 3 side chains bearing terminal 1,2,3-thiadiazole rings, respectively, have been prepared. Alkaline cleavage of 2a–c led to the corresponding alkynethiolates 6a–c, which were trapped by electrophiles such as benzyl bromide or iodomethane. The method provides an alternative to the thermal or photochemical cleavage of 1,2,3-thiadiazoles to thioketenes, which react further with nucleophiles.

chemistry.chemical_compoundNucleophileBenzyl bromideChemistryOrganic ChemistryElectrophileBenzene derivativesSide chainGeneral ChemistryPhysical and Theoretical ChemistryCleavage (embryo)Medicinal chemistryLiebigs Annalen
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ChemInform Abstract: Elemental Bromine Production by TiO2Photocatalysis and/or Ozonation.

2016

Significant production of elemental bromine (Br2 ) was observed for the first time when treating bromide containing solutions at acidic pH, with TiO2 photocatalyst, ozone, or a combination thereof. Br2 selectivities up to approximately 85 % were obtained and the corresponding bromine mass balance values satisfied. The process is general and may be applied at a laboratory scale for green bromination reactions, or industrially as a cheap, safe, and environmentally sustainable alternative to the currently applied bromine production methods.

chemistry.chemical_compoundOzoneBrominechemistryBromideInorganic chemistryPhotocatalysisHalogenationchemistry.chemical_elementTio2 photocatalystGeneral MedicineLaboratory scaleChemInform
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Light Induced Modifications of Langmuir-Blodgett-Multilayer Assemblies Containing Amphotropic Azocopolymer

1994

Abstract Photochromic LB-multilayers of amphotropic copolymers having rod-like azobenzene moieties as side groups which exhibit thermotropic liquid crystalline behaviour in the bulk have been characterized by UV-VIS spectroscopy as well as by angular dependent and energy dispersive SAXS. Upon irradiation with UV-light the initial optical in-plane anisotropy and the vertical layered structure of LB-films can be destroyed. A new layered structure can be rebuilt on irradiation with visible light or by annealing. Using linearly polarized light for the irradiation an optical anisotropy (POA) has been induced or reversibly modified by a photoselection process.

chemistry.chemical_compoundPhotochromismAzobenzeneChemistryLiquid crystalPolymer chemistryIrradiationCondensed Matter PhysicsAnisotropyPhotochemistryThermotropic crystalLangmuir–Blodgett filmVisible spectrumMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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ChemInform Abstract: Diaryldistyrylpyrazines: Solvatochromic and Acidochromic Fluorophores.

2014

Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photophysics is controlled by the styryl substitution, the diaryl substituents on the central pyrazine only having a small effect. Protonation occurs on the pyrazine and/or lateral amines or azines, thereby altering the absorption and emission properties. Hypso- and bathochromism as well as fluorescence quenching depend on the nature of the terminal substituent. This, and a significant positive solvatochromism of the fluorescence, allow optical sensing of t…

chemistry.chemical_compoundPyrazinechemistryPolarity (physics)Optical sensingSolvatochromismSubstituentProtonationGeneral MedicineAbsorption (chemistry)PhotochemistryFluorescenceChemInform
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Über Serotoninderivate mit cyclisierter Seitenkette, 1. Mitt. Darstellung der isomeren 3-(Piperidylmethyl)- und 3-(Piperidylmethyl)-5-hydroxyindole

1975

Es wird die Synthese der drei isomeren 3-(Pyridylmethyl)- und 3-(Piperidylmethyl)-5-hydroxyindole beschrieben. Die 3-(Pyridilmethyl)-5-benzyloxyindole wurden durch Kondensation von 5-Benzyloxyindolylmagnesiumbromid mit den drei isomeren Chlormethyl-pyridinbasen dargestellt. Katalytische Reduktion ihrer quartaren Salze fuhrte zu den entsprechenden Piperidinverbindungen. Die 5-Benzyloxyindole wurden durch hydrierende Debenzylierung in die 5-Hydroxyindolverbindungen ubergefuhrt. 3-(Pyridylmethyl)- and 3-(Piperidylmethyl)-5-hydroxyindoles The synthesis of the three isomeric 3-(pyridylmethyl)- and the 3-(piperidylmethyl)-5-hydroxyindoles is described. To obtain the 3-(pyridylmethyl)-3-benzyloxyi…

chemistry.chemical_compoundPyridinium CompoundsChemistryDrug DiscoveryPolymer chemistryMagnesium bromidePharmaceutical ScienceCatalysisArchiv der Pharmazie
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ChemInform Abstract: Synthesis and Self-Assembly of Novel Fluorous Cationic Amphiphiles with a 3,4-Dihydro-2(1H)-pyridone Spacer.

2011

Abstract The synthesis of fluorous (highly fluorinated) 3,4-dihydro-2(1 H )-pyridone-5-carboxylate cationic amphiphiles have been described, where the dihydropyridone serves as a spacer and either a pyridinium bromide or a triphenylphosphonium bromide form the polar cationic head group. The in water self-assembled aggregates have been observed by atomic force microscopy (AFM) and dynamic light scattering (DLS).

chemistry.chemical_compoundPyridinium bromideDynamic light scatteringAtomic force microscopyChemistryBromidePolymer chemistryAmphiphileCationic polymerizationGeneral MedicineSelf-assemblyChemInform
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Spectroscopic study of polynucleotides in cationic W/O microemulsions

2007

Water has an active and key role in determining the structure of DNA. Entrapment of DNA and of synthetic model polynucleotides in reverse micelles, where the water activity can easily be modulated, may be a useful way of assessing the influence of water on DNA characteristics; it may also offer useful ideas on the problem of how the giant DNA molecule can be confined in the limited space of cell nuclei. The quaternary microemulsion CTAB n-hexane|n-pentanol| water was used to entrap calf thymus DNA, and the model polynucleotides single-strand polyA, single-strand polyT and duplex polyAT. Ultraviolet spectros-copy, specifically the band at 260 nm, was used to compare the pairing of complement…

chemistry.chemical_compoundchemistryBase pairStereochemistryPolynucleotideHyperchromicityDenaturation (biochemistry)MicroemulsionCombinatorial chemistryMicelleDNAMacromolecule
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Oxidative halogenation of substituted pyrroles with cu(II). Part I. Bromination of some 3-acetylpyrroles

1990

3-Acetylpyrroles are brominated with copper(II) bromide. The reaction afforded almost quantitatively only nuclear monobromination. Evidence for the structures of final compounds was by mass spectrometry, 1 H-nuclear magnetic resonance, ir, and elemental analysis

chemistry.chemical_compoundchemistryBromideElemental analysisOrganic ChemistryPolymer chemistryHalogenationchemistry.chemical_elementOxidative phosphorylationMass spectrometryEnoneCopperJournal of Heterocyclic Chemistry
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Oxidative halogenation of substituted pyrroles with cu(II). Part II. Bromination of some ethyl 3-pyrrolecarboxylates and corresponding acids

1990

Ethyl 3-pyrrolecarboxylates and their corresponding acids are brominated with copper(II) bromide. The reaction afforded at 0°, with high-yield nuclear monobromination.

chemistry.chemical_compoundchemistryBromideOrganic ChemistryHalogenationOrganic chemistrychemistry.chemical_elementOxidative phosphorylationCopperJournal of Heterocyclic Chemistry
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