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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 8 (1985), S. 37-38 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Racemate separation ; Crosslinked acetylcellulose as chiral matrix ; Polarimetry ; UV-detection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0935-6304
    Keywords: Enantioselective gas chromatography ; α-Cyclodextrin ; Lactones ; O-Alkylglycerols ; Chiral pharmaceuticals ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The properties of hexakis(3-O-acetyl-2,6-di-O-pentyl)-α-cyclodextrin as a chiral stationary phase for capillary gas chromatography are described. For the first time the enantiomers of a series of different lactones are separated and their order of elution is assigned. Moreover, the enantiomers of trifluoroacetylated aldols and amino alcohols, the cyclic carbonates of 1,2-diols, 1,3-diols, O-alkylated glycerols, and some chiral pharmaceuticals are also separated on the new chiral phase. The modified α-cyclodextrin is stable above 200°C.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1986), S. 651-656 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxcarbazepine (OCB) cannot be measured undecomposed by gas chromatography, not even when injected into a cooled, inert fused-silica capillary column. The bis-trimethylsilyl derivatives of the enol of OCB and of its main metabolite, 10-hydroxy-carbazepine (10-OH-CB), and the tris-trimethylsilyl derivative of carbazepine-10,11-trans-diol (CB-trans-diol) can be obtained easily at room temperature and are well suited for gas chromatographic and gas chromatographic/mass spectrometric analysis. Thermal decomposition to the substituted iminostilbene derivatives occurs only to the extent of a few per cent under the conditions described. Two gas chromatographic/mass spectrometric assays have been developed: one for the simultaneous quantification of OCB and 10-OH-CB, the other for CB-trans-diol. Both assays use carbazepine-10,11-cis-diol as the internal standard. Using 0.5 ml of plasma, limits of detection of 0.1, 0.1 and 1 ng/ml were obtained for OCB, 10-OH-CB and CB-trans-diol, respectively. CB-trans-diol is also the main metabolite of carbamazepine in patients under maintenance therapy. The kinetics of 15N-labelled CB-trans-diol derived from a single dose of (15N)carbamazepine has been measured in plasma and urine of patients and volunteers receiving (15N)carbamazepine in several studies.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1986), S. 21-24 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to assess the feasibility of using stable 13C as a tracer for studying cholesterol metabolism in vivo (i) the 13C content of some commonly consumed foods and (ii) the stability of the 13C content of human serum cholesterol has been investigated. A procedure is described for the extraction and purification of cholesterol from food, tissues and serum suitable for 13C analysis by mass spectrometry. The method caused no significant isotope fractionation effects. Generally, there was very little difference between the carbon isotope composition of the diet, the cholesterol and the tissue from which it was derived. However, the difference in 13C composition between tissue and cholesterol of prawns from differnt parts of the world was considerable, indicating a possible peculiarity in the metabolism of cholesterol by this species. The 13C content of human serum cholesterol on a normal diet did not alter significaantly with time, suggesting that stable isotope tracer techniques could be used to measure certain aspects of cholesterol metabolism in vivo.
    Additional Material: 2 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 11 (1988), S. 506-509 
    ISSN: 0935-6304
    Keywords: Enantioselective gas chromatography ; Cyclodextrin ; Chiral pharmaceuticals ; Amines ; β-Amino acids ; Cycloalkane-trans-diols ; Inclusion phenomena ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heptakis (3-O-acetyl-2,6-di-O-pentyl)-ß-cyclodextrin is used as a chiral stationary phase in capillary gas chromatography. High enantioselectivity towards trifluoro-acetylated α and β-chiral amines, amino alcohols, α- and β-amino acid esters, and cyclic trans-diols is observed. In contrast to chiral polysiloxane phases, where hydrogen bonding interaction is essential for enantiomer separation, in cyclodextrins inclusion properties contribute to enantioselectivity. This can be concluded from the separation of N-alkylated amino compounds. The new chiral stationary phase exhibits a wide operating temperature range and is stable above 200°C.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 23 (1985), S. 130-133 
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fully proton-coupled 15N NMR spectra of pyrimidine with natural isotope abundance and of bis-labelled [1,3-15N2]pyrimidine, obtained using single pulse experiments, are described. The 15N and 1H spectra are analysed for 2J, 3J and 4J(NH) as well as N,N and H,H coupling constants.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 1077-1079 
    ISSN: 0749-1581
    Keywords: EPR ; ENDOR ; Galvinoxyl ; Coppinger's radical ; Deuteriation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of Coppinger's radical (galvinoxyl) with perdeuteriated tert-butyl groups is described. Its EPR spectrum exhibits markedly decreased line widths (0.015 mT) compared with the unlabelled radical (0.039 mT). The correspondingly higher resolution allows a complete analysis of the 13C hyperfine coupling constants. A comparison of the EPR and ENDOR spectra of unlabelled and of two selectively deuteriated Coppinger's radicals is given.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 416-424 
    ISSN: 0749-1581
    Keywords: EPR ; ENDOR ; Galvinoxyls ; Deuteriation ; Dynamic processes ; Biradicals ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The syntheses of tert-butylgalvinol with perdeuteriated tert-butyl groups and of 1,4-bicyclo[2.2.2]octanebisgalvinol are described. The EPR and ENDOR spectra of the corresponding galvinoxyl monoradicals reveal selective line broadening due to dynamic processes associated with hindered internal rotation of the phenoxy rings. Deuteriation of the central tert-butyl group in tert-butylgalvinoxyl gives rise to a substantial decrease of EPR line widths, allowing the determination of the kinetic parameters by means of line-shape analyses (ΔH≠ = 21.8 kJ mol-1, ΔS≠ = -32 J mol-1 K-1). The biradical 1,4-bicyclo[2.2.2]octanebisgalvinoxyl exhibits strong scalar and dipolar electron interactions (D = 97 MHz).
    Additional Material: 7 Ill.
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  • 9
    ISSN: 0749-1581
    Keywords: Heteronuclear Overhauser effect ; Lithioorganic compounds ; Phase sensitive ; Pseudo-steady-state ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 6Li, 1H HOESY was used both for the detection of short lithium-proton distances and for proton spectral assignments of 1,8-dilithio-1,2-diphenylhex-1-ene, which exists as a monomer-dimer equilibrium mixture in tetrahydrofuran (THF-d8). Experiments using magnitude mode, pure absorption and pseudo-steady-state mode representations are described. Pure absorption 6Li, 1H HOESY proved to be the superior method.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 409-430 
    ISSN: 0749-1581
    Keywords: NMR ; Multinuclear spin coupling ; Lone-pair effects ; Substituent effects ; Stereochemistry ; MO ; Sum-over-states models ; Electron delocalization ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nature and types of lone-pair effects on nuclear spin coupling constants are reviewed in the context of a localized bond description of molecular electronic structure. Emphasis is placed on the importance of residual delocalization involving the otherwise lone-pair orbital, in terms of which the effect of an X lone-pair, when compared with an isoelectronic Y—H or X—H+ group or with an X—R group, and its orientational dependence can be interpreted. One-, two- and three-bond coupling constants are considered and the importance of lone-pair effects for configurational and conformational information is stressed and illustrated. They also serve for a better understanding of substituent inductive effects on coupling constants.A large collection of illustrative examples are presented, with particular attention paid to couplings involving H, C, N, F and P nuclei, organized in a systematic manner into nine categories. The signs of the lone-pair effects on the reduced coupling constants are found to be independent of the actual nuclei under study in the same category. This is taken as an indication that the electron lone-pairs mainly affect the Fermi contact contribution to the coupling and, accordingly, an interpretation is given in terms of simple sum-over-states models. In addition, symmetry-based relationships are established involving the sign of lone-pair effects in coupling constants between nuclei which are a different number of bonds apart.
    Additional Material: 2 Ill.
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