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  • Wiley-Blackwell  (37)
  • Nature Publishing Group  (5)
  • American Association of Petroleum Geologists  (3)
  • 1980-1984  (39)
  • 1930-1934  (6)
  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 126 (1930), S. 761-761 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] MUNJISTHIN, a dihydroxyanthraquinone carboxylio acid occurring in Rubia tinctorum, Rubia sikkimensis, and Rubia munjistha, has been synthesised by us in the following way : 2 chloro-6-methoxy toluene (Ullmann and Pan-chaud; Annalen, 350, 108; 1906) is condensed with phthalic anhydride in ...
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 127 (1931), S. 166-166 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A MISTAKE in nomenclature has, through our inadvertence, crept into our communication on the “Synthesis of Munjisthin”, published in NATURE of Nov. 15, 1930, page 761, which we hasten to rectify. In line 6, par. 2, instead of " 2 - chloro - 3 methyl -4 methoxy ", read " 1 - chloro - 2 ...
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 125 (1930), S. 670-670 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] I HAVE read with deep interest the article by Prof. F. E. Fritsch under the title of “Research in Freshwater Biology and the Functions of a Freshwater Biological Station”, published in NATURE of Feb. 15 (vol. 125, p. 241). Work in this line is imperative in the Indian Empire. Algological ...
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 311 (1984), S. 477-480 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] We use 5'-fluorosulphonylbenzoyl[14C]adenosine(5'-Jp-FSO2bz[14C]A) to screen for kinase site-containing fragments in tryptic digests of the solubilized purified receptor10'11. This ATP analogue irreversibly modifies ATP-binding sites12'14, and inhibits phosphorylation of both the solubilized ...
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 133 (1934), S. 213-214 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] THERE is considerable difference of opinion regarding the possibility of the oxidation of nitrites by oxygen to nitrates. Berzelius reported that when aqueous solutions of alkali nitrites are boiled in air, they absorb oxygen with the formation of nitrates. G. Lunge and E. Frémy, J. ...
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 19 (1980), S. 1555-1566 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Possible conformations of lacto-N-tetraose, lacto-N-neotetraose, related disaccharides, and other milk oligosaccharides have been studied by an energy-minimization procedure using empirical potential functions. Lacto-N-tetraose favors a “curved” conformation, while lacto-N-neotetraose favors an approximately “straight” conformation. These two conformations differ mainly in the position of the terminal galactose residue with respect to the rest of the molecule. This difference explains the greater strength of lacto-N-neotetraose compared with lacto-N-tetraose in its ability to inhibit the cross-reaction of blood group P1 fractions with Type XIV pneumococcal antipolysaccharide. Although the favored conformation of lacto-N-tetraose (inactive) agrees with the model proposed by the earlier workers, that for lacto-N-neotetraose (active) differs. The favored conformations for the disaccharides galactose-β(1-4)-N-acetylglucosamine, galactose-β(1-3)-N-acetylglucosamine, and lactose are similar in overall shape, differing only in the nature and orientation of the side groups. This explains their nearly equal inhibitory activity. These theoretical models also explain the increased activity of lacto-N-fucopentaose I over that of lacto-N-tetraose and the relative activities of the substituted lactoses. The present studies suggest that it is the overall shape of the molecule which is important for activity, rather than the terminal β(1-4)-linked galactose residue alone.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 20 (1981), S. 99-121 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Possible conformations of two mannotetraoses and several milk oligosaccharides have been studied by an energy minimization procedure using semi-empirical potential functions. Changes in the terminal residue at the reducing end (cyclic to acyclic form) of these molecules do not affect the favored conformations of the remaining oligosaccharide moiety. However, differences in the overall shape of the native and reduced forms of the mannotetraose, mannose α(1-3) mannose α(1-2) mannose α(1-2) mannose are much less marked than between the native and reduced forms of lacto-N-tetraose. These differences are related to the effectiveness of the native forms as inhibitors of antibodies produced using synthetic antigens. Changes in the linkage of the residues at the nonreducing end of these molecules affect significantly the overall shape of these molecules. These differences also are related to their effectiveness as inhibitors. In the fucose-containing milk oligosaccharides the additional fucose residues only restrict the orientation of the backbone tetrasaccharide and do not push it into a totally new conformation. The fucose residues come on a surface of the molecule which is away from the region which may be important for binding. The present studies show that it is the overall shape of the molecule which is important in determining its inhibitory properties and give information as to how best to use the immune method for identification of unknown oligosaccharide sequences by specially prepared antibodies.
    Additional Material: 9 Ill.
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  • 8
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aqueous polymerization of MMA was kinetically studied using separately two complexes of sulfur dioxide as initiators, namely, quinoline-sulfur dioxide (Q-SO2) complex and tetrahydrofuran-sulfur dioxide (THF-SO2) complex. In each case the initiator exponent was 0,5 and the monomer exponent was 1,5. Kinetic data, inhibitory effect of hydroquinone, and incorporation of sulfoxy end groups in the polymers indicate a radical mechanism of polymerization with first order dependence on monomer for the rate of initiation while termination appears to take place bimolecularly.
    Additional Material: 5 Ill.
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  • 9
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was found that the Py-SO2 complex (4-140 mmol·1-1) initiates the photopolymerization of methyl methacrylate (MMA) in bulk at 40°C, the initiator exponent, kp2/kt, and the monomer exponent being 0,30, 1,27·10-2 1·mol-1·s-1, and 1,00, respectively. The radical generation is followed by an in-situ initiator-monomer complexation reaction. The kinetics of the photopolymerization of MMA were also studied using the (Py-SO2)-complex (0,01-0,35 mol·1-1) in redox combination with benzoyl peroxide (BZ2O2) (2 - 110 mmol·1-1) as initiator in the presence of variable concentrations of pyridine (1 - 7 mol·1-1). The initiation depends on the concentrations of all the reactants in the system, and the reaction order with respect to either component of the redox pair is equal to 0,5 or reasonably less than 0,5, depending on whether or not the initiating component in question is present in the system in excess compared to its counterpart in the redox combination. Variable monomer exponents, largely dependent on [BZ2O2], characterize the redox photopolymerization process. The monomer exponent value, unity at [BZ2O2] = 0, progressively decreases with increasing [BZ2O2] (non-ideal kinetics). The rate enhancing effect of the solvent pyridine is more prominent at higher [BZ2O2]. The kinetic nonidealities in each case were further analyzed and interpreted in terms of (a) primary radical termination and (b) degradative initiator transfer. Relative effects of the variation of the level of dilution with pyridine were also analyzed.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1629-1635 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Et2Zn in combination with POCl3 induces the cationic polymerization of isobutyl vinyl ether and N-vinyl carbazole at ambient temperature. The rate is directly proportional to [Et2Zn]. [POCl3] up to a mole ratio of unity of the components, and thereafter it decreases. At a fixed ratio of [Et2Zn]/[POCl3] the rate is second order in [Isobutyl vinyl ether]. Rate and [η] decrease in the presence of basic additives, pyridine, and water. Unlike the system Et3Al/POCl3, the present combination does not lead to any stereoregular poly(isobutyl vinyl ether) at ambient or lower temperatures. A cationic mechanism is proposed and an appropriate kinetic scheme is suggested.
    Additional Material: 4 Ill.
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