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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 7 (1984), S. 558-562 
    ISSN: 0935-6304
    Keywords: Gas chromatography, GC ; Capillary columns, glass ; On-column injection ; Sugars ; Oligosaccharides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sugars were separated gas chromatographically on short apolar glass capillary columns by using cold, on-column injection (OCI) techniques. After silylation, oligomers up to the hexasaccharides could be efficiently separated in resonable retention times. Response factors of silylated sugars were determined as a function of varying sample amounts and concentrations. The optimum injection amount was found to be 1 μl in heptane as solvent.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 33-36 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the 70 e V electron impact mass spectra of a series of alkyldiphenylphosphine oxides (Rφ2PO, R = Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, t-Bu, neopentyl, n-decyl), molecular ions of low abundance are observed and [M + H]+ ions are formed to a small extent at high sample pressures. The major ions include [φ2PO]+, [φ2POH]+; [φ2CH2PO]+ and [φ2CH2POH]+ which are formed by rearrangement and cleavage processes. The chemical ionization mass spectra obtained with methane and isobutane reagents consist of [M + H]+ ions. The proton affinity of Rφ2PO was found to be 219 ± 2.5 kcal mol-1.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 567-568 
    ISSN: 0749-1581
    Keywords: 13C ; NMR ; 13C,1H ; coupling constants ; 2-Acyloxy-2-alkenoates ; E/Z differentiation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical shifts and long-range 13C, 1H coupling constants to the two carbonyl C atoms were determined for a series of ethyl 2-acyloxy-2-alkenoates. The 3J(C,H) coupling constant across the double bond is 9.5-10.1 Hz for the E- and 2.9-3.8 Hz for the Z-isomer. 3J(C,H) values, therefore, may be used as a criterion for E/Z differentiation even if only one isomer is available. 13C chemical shift data, in contrast, cannot be employed for a straightforward differentiation.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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