ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 0899-0042
    Keywords: gas chromatography ; modified β-cyclodextrin column ; chiral separation ; assay ; mexiletine ; hydroxylated metabolites ; urine ; conjugation/deconjugation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The enantiomers of mexiletine and four of its hydroxylated metabolites were directly separated by capillary gas chromatography using a heptakis(6-O-tert-butyl-dimethylsilyl-2,3-di-O-methyl)-β-cyclodextrin column. The method was applied to the analysis of urine samples from cancer patients who were treated with racemic mexiletine as part of a study of the use of mexiletine in the relief of neuropathic pain. Samples analyzed before and after deconjugation of the urine with β-glucuronidase/arylsulfatase showed a high stereoselectivity in the formation and conjugation of these compounds. © 1996 Wiley-Liss, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1992 (1992), S. 1281-1287 
    ISSN: 0170-2041
    Keywords: N-Valyl-dihydroxyhomoproline ; Streptomyces antibioticus ssp. Tü 1718 B ; Antibiotics ; Peptides ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two stereoisomers (1a and 1b) of N-(L-valyl)-2′,5-dihydroxyhomoproline, the proposed structure of the dipeptide antibiotic Tü 1718 B, were synthesized by starting from natural (2S,4R)-hydroxyproline. The 1H- and 13C-NMR spectra of 1a and 1b clearly differ from the corresponding spectra of the natural product. From both synthetic stereoisomers characteristic mass spectra were obtained after esterification and trifluoroacetylation. Isomer 1a is present as a mixture of two stable conformers, as indicated by peak splitting in the1H-NMR spectra, which disappears at higher temperature, while 1b exits as a single conformer. Both synthetic stereoisomers are antibiotically inactive.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0170-2041
    Keywords: 3-Amino-4-hydroxyhexahydroazepine ; Cordyceps ophioglossoides ; Antifungals ; Antibiotics ; Ophiocordin ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (3R,4R)-3-Amino-4-hydroxyhexahydroazepine (2), the optically active constituent of the antifungal antibiotic ophiocordin (1), was prepared in a multistep synthesis starting from D-serine. The absolute configuration was unambigously assigned by a comparison of the synthesized stereoisomer 2 with its racemate and the chiral moiety of the antibiotic ophiocordin by enantioselective gas chromatography.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1040-7685
    Keywords: Enantiomers ; gas chromatography ; cyclodextrin derivatives ; temperature dependence ; capillary columns ; selectivity ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of dilution of the chiral stationary phase octakis (3-O-butyryl-2, 6-di-O-pentyl)-γ-cyclodextrin in the achiral polysiloxane OV-1701 on the separation factor was investigated over a wide concentration range. The loss in enantioselectivity was only negligible down to a dilution of 50% (w/w), since the separation factor vs. concentration curves levels off at higher concentrations. Because of the strong temperature dependence of the separation factors, the properties of short columns (10 m and 4.5 m) were evaluated. These short columns, which allow operation at low temperatures and lead to enhanced separation factors were found to be appropriate for the separations of simple mixtures, because the gain in selectivity exceeded the loss in separation efficiency. For complex mixtures, the higher efficiencies of columns of at least 25 m in length were still necessary. A plot of In α vs. 1/T did not yield straight lines, but showed a significant curvature, leading to considerable relative errors if thermodynamic data were derived from these plots.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...