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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 7 (1973), S. 1227-1234 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of N-propyl and N-butyl barbitals show the loss of olefin radical (CnH2n-1) in analogy to structurally similar molecules such as N-alkyl succinimides and 3-alkyl uracils. Trimethylsilylation of the N-substituted barbitals suppresses this fragmentation and loss of olefin via apparent McLafferty rearrangement from the even-electron ion, [M - 15]+, becomes significant. The trimethylsilyl derivatives of N-allyl barbital and N-phenyl barbital show an unusually facile elimination of the appropriate isocyanate from the molecular ion.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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