Search results for "TYR"

showing 10 items of 2017 documents

Fate of Epdxides

1982

One of the most important reactions of epoxides appears to be the covalent binding to DNA which can lead to mutagenicity and is strongly suspected to be the primary lesion ultimately leading to initiation of cancer (Miller and Miller, 1974; Oesch, 1973; Jerina and Daly, 1974; Sims and Grover, 1974; Heidelberger, 1975; Gelboin et al., 1972). This review first describes structure-activity relationships for the mutagenicity of some epoxides and then outlines some findings on the metabolic control of the concentration of such epoxides by a number of enzymes.

chemistry.chemical_classificationfungifood and beveragesCovalent bindingPolycyclic aromatic hydrocarbonCancerPrimary lesionmedicine.diseasechemistry.chemical_compoundEnzymechemistryBiochemistryStyrene oxidemedicineEpoxide hydrolaseDNA
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Muskelrelaxantien, 4. Mitt. Monoacylbutyroguanamine

1986

Die Umsetzung von Butyroguanamin (1) mit den Carbonsaureanhydriden 2a−f bei 80–120° fuhrt zu den Monoacylbutyroguanaminen 3a−f, deren Struktur durch IR-, 1H-NMR- und MS-Spektren untermauert wird. Unter den hier beschriebenen Verbindungen weisen insbesondere 3e muskelrelaxierende und antidiabetische und 3a trichomonazide und antivirale Wirksamkeit auf, wahrend mit 3b−d herbizide Wirkungen beobachtet werden. Muscle Relaxants, IV: Monoacylbutyroguanamines Reaction of butyroguanamine (1) with the carboxylic acid anhydrides 2a−f at 80–120°C leads to the monoacylbutyroguanamines 3a−f, the structure of which is supported by IR, 1H-NMR, and mass spectra. Among the compounds described here, particul…

chemistry.chemical_classificationmedicine.drug_classCarboxylic acidPharmaceutical ScienceMuscle relaxantCarboxamideBiological activityButyroguanamineNuclear magnetic resonance spectroscopyMedicinal chemistryAcylationchemistryDrug DiscoverymedicineMass spectrumArchiv der Pharmazie
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Bulk morphologies of polystyrene-block-polybutadiene-block-poly(tert-butyl methacrylate) triblock terpolymers

2015

Abstract The self-assembly of block copolymers in the bulk phase enables the formation of complex nanostructures with sub 100 nm periodicities and long-range order, both relevant for nanotechnology applications. Here, we map the bulk phase behavior of polystyrene-block-polybutadiene-block-poly(tert-butyl methacrylate) (SBT) triblock terpolymers on a series of narrowly distributed polymers with widely different block volume fractions, ϕS, ϕB and ϕT. In dependence of ϕ, we find the lamella–lamella, core-shell cylinder, cylinder-in-lamella and core-shell gyroid morphology, but also a rarely observed cylinder-in-lamella phase. The bulk morphologies are thoroughly characterized by transmission e…

chemistry.chemical_classificationta214Materials scienceta114Polymers and PlasticsSmall-angle X-ray scatteringta221Organic Chemistryblock copolymerPolymerMethacrylateCrystallographychemistry.chemical_compoundPolybutadienesmall-angle x-ray scattering (SAXS)Chemical engineeringchemistryPhase (matter)morphologytransmission electron microscopy (TEM)Materials ChemistryCopolymerPolystyreneta218GyroidPolymer
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Fast Response Heating Module for Temperature Programmed GC Analysis in Microreaction Systems

2000

For monitoring the reactant and product concentrations of a gas phase microreactor for ethylene oxide synthesis the development of a miniaturised device for fast GC analysis suitable for operation in conjunction with the microreactor is advantageous. Therefore, a method employing short (0.2 – 0.4 m) packed capillary columns was developed. Highly crosslinked polystyrene microspheres proved to be the most suitable adsorbent enabling a high separation efficiency. For fast temperature programming design concepts for an efficient heating module capable to be used with short capillary columns were developed. In principle, planar as well as cylindrical designs are suitable for integration of a res…

chemistry.chemical_compoundAdsorptionPlanarMaterials scienceChemical engineeringEthylene oxidechemistryCapillary columnCapillary actionPolystyrene microsphereMicroreactorJoule heating
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ChemInform Abstract: Hydrophobically Directed Aldol Reactions: Polystyrene-Supported L-Proline as a Recyclable Catalyst for Direct Asymmetric Aldol R…

2008

A simple synthetic methodology for the preparation of a polystyrene-supported L-proline material is reported, and this material has been used as catalyst in direct asymmetric aldol reactions between several ketones and arylaldehydes to furnish aldol products in high yields and stereoselectivities. Screening of solvents showed that these reactions take place only in the presence of water or methanol, at lower levels of conversion in the latter case. This solvent effect, coupled with the observed high stereoselectivities, has been explained in terms of the formation of a hydrophobic core in the inner surface of the resin, whereas the hydrophilic proline moiety lies at the resin/water interfac…

chemistry.chemical_compoundAldol reactionChemistryMoietyOrganic chemistryStereoselectivityGeneral MedicineProlinePolystyreneMethanolSolvent effectsCatalysisChemInform
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Theoretische analyse der bei einem zweiwegwachstumsmechanismus auftretenden molekulargewichtsverteilungen und ihre anwendung auf die anionische polym…

1967

Es werden mittels der Momentmethode die fur einen abbruchfreien Zweiwegwachstumsmechanismus zu erwartenden Molekulargewichtsverteilungen und ihr Zusammenhang mit dem kinetischen Ablauf theoretisch abgeleitet. Die ermittelten Bezichungen werden auf das Polymerisationssystem Styrol in Cumylmethylather mit Cumylnatrium als Initiator angewandt. Durch Einsetzen der vorher experimentell ermittelten kinetischen Daten in die theoretisch abgeleitete Gleichung werden die Molekulargewichtsverteilungen des untersuchten Systems berechnet und mit den experimentell ermittelten verglichen. Die gute Ubereinstimmung zwischen Theorie und Experiment stellt einen schlussigen Beweis fur das Vorliegen eines Zweiw…

chemistry.chemical_compoundAnionic addition polymerizationPolymerizationChemistryPolymer chemistryEtherStyreneDie Makromolekulare Chemie
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Herstellung, charakterisierung und lösungseigenschaften von einheitlichen styrol-α-methylstyrol block-copolymeren

1977

An improved anionic polymerization technique for the preparation of highly uniform styrene/α-methylstyrene linear two-block copolymers is described. Three sets of samples with molecular weights M were prepared under equal experimental conditions, namely polystyrenes (2 · 105 < M < 3 · 106), poly(α-methylstyrene)s (7 · 104 < M < 4 · 106), and block copolymers (2 · 105 < M < 2,5 · 106). Ultracentrifugation in a density-gradient does not show any chemical heterogeneities in the block copolymers. The molecular polydispersity U = Mw/Mn–1 is U = 0,03 or less as estimated from GPC-measurements. The high molecular and chemical homogeneity of the block copolymers and the optical similarity of the tw…

chemistry.chemical_compoundAnionic addition polymerizationVirial coefficientchemistryIntramolecular forceDispersityPolymer chemistryCopolymerGyrationTolueneStyreneDie Makromolekulare Chemie
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Some comments on the article of A. A. Korotkov and A. F. Podolsky: On the mechanism of the anionic polymerization of styrene with “living” polystyren…

1966

chemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryGeneral EngineeringPolystyreneMechanism (sociology)StyreneJournal of Polymer Science Part B: Polymer Letters
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Polymerisationskinetische und konduktometrische messungen an polystyrylionenpaaren in einem größeren temperaturbereich

1974

Messungen der Bruttogeschwindigkeitskonstante von Polystyryl-Natrium in 3-Methyltetrahydrofuran (3-Me-THF) in Abhangigkeit von der Konzentration der “lebenden” Kettenenden und der Natriumionen ergeben, das die Monomeraddition wie in anderen polaren Losungsmitteln nach einem Mehrwegmechanismus erfolgt. Der Ubergang vom Kontakt- zum solvatgetrennten Ionenpaar wird in einem Temperaturbereich von — 110 bis +85°CC mit Hilfe kinetischer Messungen im Stromungsrohr und durch Leitf ahigkeitsmessungen verfolgt. Analog zu entsprechenden Untersuchungen in Tetrahydrofuran kann dabei die Polymerisation uber jeweils eine Art von Ionenpaaren fast vollstandig isoliert beobachtet werden. Die thermodynamische…

chemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPolymerization kineticsKineticsPolymer chemistryConductanceAtmospheric temperature rangeTetrahydrofuranStyreneDie Makromolekulare Chemie
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Kinetik der anionischen Polymerisation von Styrol in Dioxan mit Polystyryl-Natrium als Reaktionträger

1971

Die Wachstumskonstante des Polystyryl-Natriums bei der Polymerisation von Styrol in Dioxan wird als Funktion der Konzentration der „lebenden” Enden und der Temperatur gemessen und mit den entsprechenden Werten in anderen Losungsmitteln verglichen. Es zeigt sich, das die Polymerisation in Dioxan ausschlieslich uber das Kontaktionenpaar verlauft. The propagation rate constants of the anionic polymerization of styrene in dioxane were measured as a function of the “living” end concentration and of the temperature. They were compared with corresponding values in other solvents. It is shown that only contact ion-pairs are involved in this polymerization.

chemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPropagation ratePolymer chemistryStyreneDie Makromolekulare Chemie
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