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  • Artikel  (99)
  • Wiley-Blackwell  (99)
  • 1990-1994  (99)
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  • Artikel  (99)
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  • 1
    ISSN: 1042-7163
    Schlagwort(e): Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: We have prepared two new tetracyclic phenylboronic esters 4 and 5 derived from myo-inositol and from 1,2-O-isopropylidene-myo-inositol, respectively. The structures of these compounds were established from NMR and IR spectra, elemental analyses, and an X-ray diffraction study in the case of 4. Compound 4 is a tetracyclic derivative of the less stable conformer of inositol (five axial hydroxy groups and one equatorial) with two dioxaboroline rings at opposite faces of the six-membered ring, one formed between the boron atom and the axial hydroxyl groups at C-3 and C-5 and the other between the boron atom and the hydroxyl groups at C-4 and C-6, and a dioxaborolidine ring bridging C-1 and C-2 at axial and equatorial positions. A similar structure was found for 5 with the difference that bridging C-1 and C-2 there is a dioxolane ring. The boron atoms are planar with their attached atoms, stabilized by retrocoordination between the boron and oxygen and carbon atoms, respectively. The two phenyl rings that are in the same face of the molecule are essentially parallel, with a dihedral angle between planes of 28.26 ± 0.79°.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 0951-4198
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: The main fragmentation pathway of vinyl triflates in mass spectra involves the loss of CF3SO2·, followed by the loss of olefin and/or CO. The loss of TfOH takes place with fragmentation of a vinylic C—H bond. TfOH2+ ions are formed via regiospecific double hydrogen transfer from five- and six-membered cyclic triflates.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 237-238 
    ISSN: 0030-493X
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    ISSN: 0049-8246
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Physik
    Notizen: This work suggests a theoretical approach for the description of a primary x-ray beam by means of the K fluorescence which it excites on a set of thin targets made of pure elements. Physical quantities, defined as weighted integrals over hv of the photon spectral distribution, are obtained directly as weighted integrals of the Kα yields over the variable Ez (the ionization energy of the K shell of the element with atomic number Z), without needing any explicit reconstruction of the spectral distribution. The set of Kα yields produced by an x-ray beam as a function of Ez is a functional description of the exciting beam. Theoretically, such a description is suited to x-ray fluorescence analysis.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 161 (1994), S. 129-141 
    ISSN: 0021-9541
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: NIH-3T3 cells transfected with yeast H+-ATPases (RN1A cells) are tumorigenic (Perona and Serrano, 1988, Nature, 334: 438). We have previously shown that RN1a cells maintain a chronically high intracellular pH (pHin) under physiological conditions. We have alsoshown that RN1a cells are serum-independent for growth, maintain a higher intracellular Ca2+(in), and glycolyze more rapidly than their non-transformed counterparts (Gillies et al., Proc. Natl. Acad. Sci., 1990, 87: 7414; Gillies et al., Cell. Physiol. Biochem., 1992, 2: 159). The present study was aimed to understand the interrelationships between glycolysis, pHin, and [Ca2+]in in RN1a cells and their non-transformed counterparts, NIH-3T3 cells. Our data show that the higher rate of glycolysis observed in RN1a cell is due to the presence of low affinity glucose transporters. Consequently, the higher rate of glycolysis is exacerbated at high glucose concentration in RN1a cells. Moreover, the maximal velocity (Vmax) for glucose utilization is up to sixfold higher in RN1a cells than in the NIH-3T3 cells, suggesting that the number of glucose transporters is higher in RN1a than NIH-3T3 cells. Glucose addition to NIH-3T3 cells results in modest decreases in both pHin and [Ca2+]in. In contrast, RN1a cells respond to glucose with a large decrease in pHin, followed by a large decrease in [Ca2+]in. The decrease in [Ca2+]in observed upon glucose addition is likely due to activation of Ca2+-ATPase by glycolysis, since the Ca2+ decrease is abolished by the Ca2+ ATPase inhibitors thapsigargin and cyclopiazonic acid. Glucose addition to ATP-depleted cells results in a decrease in [Ca2+]in, suggesting that ATP furnished by glycolysis is utilized by this pump. © 1994 Wiley-Liss, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    ISSN: 0021-9541
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: The role of intracellular pH (pHin) in the regulation of cell growth in both normal and transformed cells is a topic of considerable controversy. In an effort to study this relationship NIH 3T3 cells were stably transfected with the gene for the yeast H+-ATPase, constitutively elevating their pHin. The resulting cell line, RN1a, has a transformed phenotype: The cells are serum independent for growth, clone in soft agar, and form tumors in nude mice. In the present study, we further characterize this system in order to understand how transfection with this proton pump leads to serum-independent growth, using defined media to investigate the effects of specific growth factors on the transfected and parental NIH 3T3 cells. While both cell lines show similar growth increases in response to platelet-derived growth factor (PDGF)-BB and epidermal growth factor (EGF), they respond differently to insulin, insulin-like growth factor-I (IGF-I) and PDGF-AA. RN1a cells exhibit increased growth at nanomolar concentrations of insulin but the parental cells had only a relatively minor response to insulin at 10 μM. Both cell lines showed some response to IGF-I in the nanomolar range but the response of RN1a cells was much larger. Differences in insulin and IGF-I receptor number alone could not explain these results. The two cell lines also respond differently to PDGF-AA. RN1a cells are relatively insensitive to stimulation by PDGF-AA and express fewer PDGF α receptors as shown by Northern blots and receptor-binding studies. We propose a unifying hypothesis in which the H+-ATPase activates a downstream element in the PDGF-AA signal transduction pathway that complements insulin and IGF-I signals, while leading to downregulation of the PDGF α receptor. © 1994 wiley-Liss, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    ISSN: 0749-1581
    Schlagwort(e): 1H, 13C, 15N and 113Cd NMR ; Two-dimensional NMR ; CP/MAS NMR ; Hg and Cd complexes 4(1H) -Quinazolinone-2,3-dihydro-2-thioxo ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Cd(II) and Hg(II) complexes of 4(1H)-quinazolinone-2,3-dihydro-2-thioxo (1) and the free ligand were studied by 1D and 2D multinuclear magnetic resonance in solution and 13C cross polarization magic angle spinning NMR in the solid state. Compound 1 adopts only one of five possible tautomeric structures in solution, namely the thiouracyl-like structure. It was found that the metal atom is linked to two molecules of deprotonated 1 by N-1 and coordinated by the sulphur atom. The compounds retain the same structure in the solid state and in dimethyl sulphoxide solution.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 178 (1990), S. 1-16 
    ISSN: 0003-3146
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Die seit langem in der Literatur als “Indophenin-Reaktion” bekannte Umsetzung von Isatin mit Thiophen wurde systematisch untersucht und auf die Umsetzung mit Bithiophen erweitert. Die Reaktionsprodukte wurden isoliert und durch FT-IR, UV, 1H-NMR, 13C-NMR sowie GPC charakterisiert.Im Gegensatz zu den Literaturdaten wurden Reaktionsprodukte mit höheren Molgewichten und anderer Molmassenverteilung gefunden. Die Reaktionsbedingungen - Lösungsmittel, Temperatur und Konzentration - sind für den Reaktionsablauf und die entstehenden Produkte von entscheidender Bedeutung.Füur die oligomeren Reaktionsprodukte werden neue Strukturen vorgeschlagen, die in Übereinstimmung mit allen analytischen Daten sind. Anhand eines Formelschemas werden die Reaktionen des Isatins mit Thiophen (Bithiophen) erläutert.
    Notizen: A systematic study of the well-known indophenin reaction between isatin and thiophene was extended to embrace bithiophene. The products of the reactions were isolated and characterized by FT-IR, UV, 1H-NMR, 13C-NMR, and GPC. The values of the thus determined molar masses and molar mass distributions differed from the data given in the literature. The reaction conditions - solvent, temperature, and concentration - are of crucial importance for the course of the reaction and the products obtained.New structures suggested for the oligomeric reaction products agree with all the analytical data. The reactions between isatin and thiophene (bithiophene) are explained schematically.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The translational and rotational diffusion coefficients and the intrinsic viscosity of semiflexible, randomly broken, and wormilike chains have been obtained by Monte Carlo simulation in the context of the rigid-body treatment. Both approximate and rigorous rigid-body hydrodynamics are used, so that the error introduced by the approximate methods can be evaluated. A randomly broken chain and a wormilike chain having the same contour length and persistence length have the same radius of gyration but different values for any of the hydrodynamic properties. The two types of chains are compared in this regard. Considering that the cross section of the chain is represented by a cylinder better than by a string of spheres, we devise a cylindrical correction to be applied to the results simulated for chains of beads. Application is made to the analysis of experimental data for the translational and rotational coefficients of DNA fragments with up to 103 base pairs, obtaining the persistence length for each model. The values for the wormlike chain agree well with model-independent values obtained from radii of gyration and with other literature data at varying ionic strength. The randomly broken chain is equally able to reproduce the experimental length dependence of the properties, but the resulting persistence length may be too high.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    ISSN: 0009-2940
    Schlagwort(e): Dithiazinanes ; Dithiazoniaboratacyclohexane ; Amines: dimethylation and monodeuteriomethylation ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 5-Methyl-and 5-tert1-butyl-1,3,5-dithiazinane (1 and 7) react with BH3·THF, and Et2O·BF3 to yield the N1-coordinated adducts 2 - 4 (with BH3, BD3, and BF3, respectively). The conformations and spectroscopic properties of the adducts are discussed. The reactions of 1 and 7 with BY3·THF lead to the six-membered boron heterocycles 5,5-dimethyl-1,3-dithia-5-azonia-4-boratacyclohexane (5), 4,4-dideuterio-5-methyl-5[D1]methyl-1,3-dithia-5-azonia-4-boratacyclohexane (6), and 5-tert1-butyl-5-methyl-1,3-dithia-5-azonia-4-boratacy-clohexane (8). Compounds 2 and 5 are isolobal isomers. The reaction of BH3 or BD3 with 7 affords, after heating, tert1-butyldimethylamine - borane (9) and tert1-butyldi([D1]methyl)1-amine - trideuterioborane (11), respectively. The dithiazinane derivatives may be used in organic synthesis for the dimethylation of primary amines and the preparation of alkyldimethylamines with monodeuterated methyl groups.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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