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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 2 (1990), S. 275-279 
    ISSN: 0899-0042
    Keywords: nucleotide analogue ; antiviral ; chiral separation ; complexation ; ion-pairing ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An acylonucleotide analogue, 1-[3-hydroxy-2-(phosphonyl-methoxy)propyl]cytosine (HPMPC), has shown activity against herpes simplex Type I and Type II viruses. An HPLC separation of the R- and S-enantiomers of HPMPC by ligand exchange using a mobile phase containing phenylalanine as the chiral modifier and copper(II) as the metal ion is reported.
    Additional Material: 4 Ill.
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  • 2
    ISSN: 0886-9383
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 5 (1991), S. 545-545 
    ISSN: 0886-9383
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 5 (1991), S. 263-268 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The use of collisional-activation dissociation (CAD) in the electrospray region was evaluated for generating structural information on several pesticides and antibiotics. The collision energy used to generate the CAD spectra could be varied easily by changing the capillary/skimmer potential difference, imparting fromOeV to above 16 eV internal energy to the near thermal ions generated by electrospray, The internal energy distribution for low-energy collisions (capillary/skimmer potential difference of 20 V) closely matches the curves generated by a triple-quadrupole mass spectrometer. Furthermore, the CAD spectra for selected compounds generated by electrospray in the transport region at a capillary/skimmer potential differences of 30-50 V closly resembled those obtained from the [M + H]+ ion by a triple quadrupole using 30eV collision energy. The CAD of ions in the transport region resulted in 70% to 80% daughter-ion yields and minimal loss in overall ion current compared to the ion current for protonated or cationized parent molecules. The major daughter ions for 10 pg of Aldicarb and penicillin G could be detected (signal-to-noise ratio〉5) under full-scan CAD conditions.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 102 (1969), S. 1892-1903 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enoläther mit mindestens einem Wasserstoffatom in Allylstellung tauschen dieses mit N-Brom-succinimid (NBS) in CCl4 in einem ionischen Additions-Eliminierungs-Mechanismus gegen Brom aus (im Gegensatz zur bekannten radikalischen Reaktion bei Olefinen). Gründe für die Addition bzw. Eliminierung werden anhand zahlreicher Beispiele diskutiert. Die Thermolyse der Addukte liefert in Abhängigkeit von der Struktur des Ausgangsenoläthers Bromenoläther, α-Brom- oder α.β-ungesättigte Carbonylverbindungen.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 38 (1990), S. 133-143 
    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: Molecular mechanics calculations have been used to study the external noncovalent complexes formed between DNA and the strong carcinogen, aflatoxin B1. Three different sequences of hexameric duplexes were used for the DNA. Both the aflatoxin B1 parent molecule and its ultimate carcinogenic form, a carbocation, were modeled. The results are compared with recent experimental data on sequence specificity of the covalent attachment of aflatoxin to sites on the nucleotide bases. The comparison is discussed in light of a recently proposed hypothesis suggesting that the locus of carbocation formation is in acidic domains near the surface of the macroion and this determines the site of covalent adduct formation.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 44 (1992), S. 1-14 
    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: Kinetic studies of the hydrolysis of benzo[a]pyrene diol epoxides have shown that hydrolysis proceeds through an acid-catalyzed SN1 mechanism and that the rate-determining step is the formation of a benzylic carbocation. The formation of this carbocation indicates that the diol epoxide can react with nucleophilic sites on DNA as an alkylating agent. Previous work has indicated that the kinetic data could be accurately fit to kobsd = kH [H+] + k0, in which kH [H+] is the pseudo first-order rate constant for acid-catalyzed hydrolysis and k0 is the rate constant for spontaneous hydrolysis. The observation made in several laboratories, that DNA catalyzes the hydrolysis of carcinogenic diol epoxides, is of direct interest in light of our recent calculation indicating that the local environment of DNA has a high concentration of hydrogen ions. The significance of acidic domains around nucleic acids is primarily in the ability of the protons to catalyze reactions. We have hypothesized that the high concentration of hydrogen ions at the DNA surface is responsible for the catalysis and that the generation of benzylic carbocations at the DNA surface can result in either nontoxic tetraols or in mutagenic nucleotide adducts, depending on the nucleophile with which the carbocation reacts. The calculations presented here are concerned with qualitatively understanding the rate constants in terms of the mechanisms of the acid-catalyzed and the spontaneous (H2O-catalyzed) hydrolyses. © 1992 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 48 (1993), S. 213-230 
    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: Metropolis Monte Carlo and Poisson-Boltzmann calculations were done to quantitatively assess the conditions under which counterion condensation (CC) theory could be considered valid. The fundamental prediction of condensation theory, that the number of counterions bound to a polyelectrolyte molecule can be predicted by a single parameter describing the linear charge density of the charged system, was shown to be quantitatively correct for a range of conditions. To define the number of counterions bound, it was necessary to use an energy-based criterion by which ions that interact with the polyion with an energy less than -kT were considered bound. Using this criterion, Monte Carlo calculations on systems consisting of charged cylinders and a neutralizing number of counterions in a dielectric continuum showed that the number of bound counterions was quantitatively predictable by the CC relation (1-1/ξ) for systems with a linear charge density and dimensions approaching those of duplex or triplex DNA. Poisson-Boltzmann (PB) calculations on cylinders with different linear charge densities and radii have been done to assess the limits of the CC prediction that the number of counterions bound is a constant even as the bulk concentration of electrolyte in the surrounding is increased. As in the case of the MC calculations, the validity of the CC prediction is seen to increase with increasing linear charge density of the charged cylinder. The agreement between PB and CC is seen to be very good for highly charged cylinders. The results described here provide justification for the use of CC theory for interpreting experimental data on polyelectrolytes of the approximate dimensions and linear charge density of duplex or triplex DNA. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 56 (1995), S. 29-37 
    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: The aziridine analogues of the epoxide metabolites of carcinogenic polycyclic aromatic hydrocarbons have greater mutagenic potency than the epoxides. Like their well-studied analogues, the aziridines undergo a pH-dependent decomposition that leads to a reactive carbocation intermediate. In aqueous solution the nucleophile with which the carbocation generally reacts is water. The kinetics of this pH-dependent reaction have been experimentally characterized by others. Although the effect of DNA on this reaction has not been studied, we hypothesize that, like their epoxide analogues, the aziridine derivatives of polycyclic aromatic hydrocarbons undergo a DNA-catalyzed reaction leading through a carbocation to either a DNA-adduct or a hydrolysis product. Using Poisson-Boltzmann calculations in conjunction with Metropolis Monte Carlo simulations and energy-minimized conformations, we predict the DNA-dependence of the acidcatalyzed decomposition of the K-region aziridine, phenanthrene[9,10]imine. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 65 (1997), S. 1087-1093 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Recent work by the authors on the calculation of local solvent dielectric constants around polyelectrolytes using the Poisson-Boltzmann approach is analyzed in terms of the effect on surface potentials and counterion concentrations. Polyelectrolyte surface geometry, local electric fields, and counterion distributions contribute to the self-consistent prediction of local solvent dielectric constants. For an all-atom cell model of DNA with added monovalent salt varying from 0 to 0.5M, the Poisson-Boltzmann-determined electrostatic potential increases (negatively) by 50-100% upon the inclusion of local dielectric constants. This, in turn, implies that hydronium ion concentrations in the major and minor grooves increase by about 0.65 and 0.35 pH units, respectively. While counterion concentrations in the major groove change only slightly, those in the minor groove increase by 60-90%. It is also noted that while the local dielectric constant in the major groove monotonically increases away from the surface toward the bulk value of water the dielectric constant in the minor groove has a minimum about 2 Å from the surface due primarily to the local electric field. Certain other properties, such as ionic and dipole first passage times, are affected little by local dielectric constants (less than about 3%).   © 1997 John Wiley & Sons, Inc. Int J Quant Chem 65: 1087-1093, 1997
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