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  • Chemical Engineering  (92)
  • Organic Chemistry  (55)
  • GENERAL
  • 1990-1994  (110)
  • 1960-1964
  • 1955-1959  (51)
  • 1925-1929
  • 1991  (110)
  • 1955  (51)
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  • 1990-1994  (110)
  • 1960-1964
  • 1955-1959  (51)
  • 1925-1929
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 1895-1899 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 1900-1903 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 3 (1991), S. 412-417 
    ISSN: 0899-0042
    Keywords: pirprofen enantiomers ; human serum albumin ; binding ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interaction of pirprofen enantiomers with human serum albumin (HSA) was investigated by means of high-performance liquid chromatography (HPLC), circular dichroism (CD), and 1H NMR spectroscopy. HPLC experiments indicated that both pirprofen enantiomers were bound to one class of high-affinity binding sites (n(+) = 1.91 ± 0.13, K(+) = (4.09 ± 0.64) × 105 M-1, n(-) = 2.07 ± 0.13, K(-) = (6.56 ± 1.35) × 105 M-1) together with nonspecific binding (n′K′(+) = (1.51 ± 0.21) × 104 M-1, n′K′(-) = (0.88 ± 0.13) × 104 M-1). Slight stereoselectivity in specific binding was demonstrated by the difference in product n(+)K(+) = (0.77 ± 0.08) × 106 M-1 vs. n(-)K(-) = (1.30 ± 0.21) × 106 M-1, i.e., the ratio n(-)K(-)/n(+)K(+) = 1.7. CD measurements showed changes in the binding sites located on the aromatic amino acid side chains (a small positive band at 315 nm and a pronounced negative extrinsic Cotton effect in the region 250-280 nm). The protein remains, however, in its predominantly alpha-helical conformation. The 1H NMR difference spectra confirmed that both pirprofen enantiomers interacted with HSA specifically, most probably with site II on the albumin molecule.
    Additional Material: 3 Ill.
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  • 4
    ISSN: 0899-0042
    Keywords: ketoprofen ; stereoisomers ; plasma binding ; binding linearity and competition ; ketoprofen glucuronides ; 2-arylpropanoic acids ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The protein binding of ketoprofen enantiomers was investigated in human plasma at physiological pH and temperature by ultrafiltration. 14C-labelled (RS)-ketoprofen was synthesized and purified by high-performance liquid chromatography and utilized as a means of quantifying the unbound species. In vitro studies were conducted with plasma obtained from six healthy volunteers. The plasma was spiked with (R)-ketoprofen alone, (S)-ketoprofen alone, and (RS)-ketoprofen in the enantiomeric concentration range of 1.0 to 19.0 μg/ml. The plasma protein binding of ketoprofen was nonenantioselective. At a racemic drug concentration of 2.0 μg/ml the mean (± SD) percentage unbound of (R)-ketoprofen was 0.80 (± 0.15)%. The corresponding value for (S)-ketoprofen, 0.78 (± 0.18)%, was not statistically different (P 〉 0.05). At this racemic drug concentration (2.0 μg/ml) the percentage unbound of each enantiomer was unaffected (P 〉 0.05) by the presence of the glucuronoconjugates of ketoprofen (10 μg/ml) in plasma. At clinically relevant concentrations, the plasma binding of ketoprofen did not exhibit enantioselectivity or concentration dependence nor was the binding of either enantiomer influenced by its optical antipode (P 〉 0.05).
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 592-595 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Reinforced plastics based on poly(cyclohexanedimethylene terephthalate) (PCT) are excellent for electrical and electronic applications, particularly in the manufacture of electrical connectors. PCT offers a high heat deflection temperature, low cost, and relative ease of processing. For the injection molding process, stability of the melt is an important consideration, especially for materials with high melting points such as PCT. The combination of the polyester resin with flame retardant additives, processing aids, and thermal stabilizers results in a number of competing reactions which can change the molecular weight and molecular-weight distribution (MWD) of the base polymer in the composite. Typical analytical techniques such as melt or dilute solution viscosity do not give adequate means of monitoring these changes so as to allow the polymer chemist to determine the effects of various additives on MWD. Size-exclusion chromatography (SEC), by virtue of providing information on the entire MWD, was found suitable to study molecular-weight changes in the melt due to both branching and chain cleavage, even when both phenomena occur simultaneously. Changes in the MWD over time at processing temperatures can be used to determine kinetic parameters and have been used to optimize PCT additive formulations for best processability and mechanical property retention.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 1665-1669 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The Differential Scanning Calorimetry (DSC) trace for a commercial phenolic resole resin shows two distinct peaks. Assuming that these represent two independent cure reactions results in a kinetic model of the form: \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{{dx}}{{dt}} = p\kappa _1 \left({1 - x_1} \right)^{n_1} + \left({1 - p} \right)\kappa _2 \left({1 - x_2} \right)^{n_2} $$\end{document} with κi = κio exp(-Bi/T).The Arrhenius parameters were estimated from a plot of ln(β/Tp2) versus 1/Tp. The parameters, p, n1, and n2 were obtained by writing the DSC response predicted by the equation above in terms of a function which contains temperature as the only variable. \documentclass{article}\pagestyle{empty}\begin{document}$$ \dot q = q_{tot} \left[{p\kappa _1 \left({1 - \theta _1 /r_1} \right)^{r_1 - 1} + \left({1 - p} \right)\kappa _2 \left({1 - \theta _2 /2} \right)^{r_2 - 1}} \right] $$\end{document} with \documentclass{article}\pagestyle{empty}\begin{document}$ \theta _i = \left({1/\beta} \right)\int_{T_0}^T {\kappa _i dT \le r_i} $\end{document} dT ≤ ri and ri = 1/(1-ni).Fitting this equation to the DSC response measured at a scan rate of 4°C/min obtains p ≈ 0.66; n1 ≈ 0.55; n2 ≈ 2.2; B1 ≈ 8285; B2 ≈ 7480; κ1 ≈ 1. 12 × 108 s-1; κ2 ≈ 0.99 × 106 S-1.
    Additional Material: 3 Ill.
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  • 7
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus dem Kulturfiltrat von Streptomyces narbonensis n. sp. wurde ein neues lipophiles kristallines basisches Antibioticum C28H47O7N, das Narbomycin, isoliert.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 38 (1955), S. 1445-1448 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus Kulturfiltrat und Mycel eines Streptomyces viridochromogenes oder Streptomyces olivochromogenes nahestehenden Streptomyceten wurde neben Actidion eine neutrale, farblose, kristalline Verbindung C30H48O9, das Nonactin, isoliert, die chemisch wenig reaktiv ist und gegenüber den untersuchten Mikroorganismen unwirksam oder nur schwach wirksam war.
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 38 (1955), S. 1202-1209 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus dem Kulturfiltrat von Streptomyces eurythermus n. sp. konnte ein neues lipophiles kristallines basisches Antibioticum C50±1H89±2O18N, das Angolamycin, isoliert werden.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 333 (1991), S. 139-143 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of 4-Chloromethyl-1,3-dioxolanes with Sulfur and Nitrogen Containing Nucleophiles.
    Additional Material: 2 Tab.
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