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  • 1
    Electronic Resource
    Electronic Resource
    Fe(III) complexes of d-glucose and d-fructose (1994)
    Springer
    BioMetals 7 (1994), S. 25-29 
    Details
    ISSN: 1572-8773
    Keywords: complexes ; Fe(III) ; fructose ; glucose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Fe(III)-saccharide complexes of d-glucose and d-fructose have been synthesized from methanol using stoichiometric quantities of sodium salts of the corresponding saccharides. Both the compounds were isolated in the solid state and characterized by various analytical, spectroscopic, magnetic and cyclic voltammetric methods. Both the complexes were found to be stable, in solution, in the pH range 2.5–12.0.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00205190
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  • 2
    Electronic Resource
    Electronic Resource
    Infrared spectroscopic study of C7 intramolecular hydrogen bonds in peptidesContribution No. 156 from the Solid State and Structural Chemistry Unit. (1983)
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 2091-2104 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ir-spectra in the N—H stretching region of Piv-Pro-NHMe and Boc-Pro-NHMe have been studied in carbon tetrachloride and chloroform solutions over a wide range of concentrations. Based on the concentration dependence of the N—H stretching bands, it has been shown that the characteristic N—H stretching band due to the C7 intramolecular hydrogen bond is around 3335 cm-1. Intermolecular hydrogen bonding also occurs to a small extent in these peptides, giving rise to a slight concentration dependence of the N—H stretching bands. The band around 3335 cm-1 need not necessarily be due to C7 hydrogen bonds alone as proposed by Tsuboi et al. or to intermolecular hydrogen bonding alone as proposed by Maxfield et al.; this conclusion is supported by studies on Boc-Leu-NHMe, which undergoes only intermolecular hydrogen bonding. We have shown that Z-Aib-Aib-OMe and Z-Aib-Ala-OMe form C7 intramolecular hydrogen bonds in addition to C5 intramolecular hydrogen bonds. The present studies also show that all the peptides studied exist in more than one conformation in solution.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360220908
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  • 3
    Electronic Resource
    Electronic Resource
    Molecular structure of t-butyloxycarbonyl-Leu-Aib-Pro-Val-Aib-methyl ester, a fragment of alamethicin and suzukacillin: A 310-helical pentapeptide (1982)
    New York : Wiley-Blackwell
    Biopolymers 21 (1982), S. 2461-2472 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pentapeptide Boc-Leu-Aib-Pro-Val-Aib-OMe, a fragment of alamethicin and suzukacillin, crystallizes in the space group P21, with a = 11.034 (2), b = 10.894 (2), c = 15.483 (2) Å, β = 104.80 (2)° and Z = 2. The crystal structure has been solved by direct methods and refined to an R value of 0.069. The peptide backbone folds into a right-handed 310-helical conformation, stabilized by two intramolecular 4 → 1 hydrogen bonds between the Leu(1) CO and Val(4) NH and Aib(2) CO and Aib(5) NH groups. The solid-state conformation is consistent with results of spectroscopic analysis in solution.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360211210
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