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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 247-251 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of 1-aryl-5-amino-4,5-dihydro-v-triazoles bearing at least one hydrogen atom at the C-4 position has been prepared. The NMR features of the above compounds have been studied with the purpose of differentiating the triazolines with a trans configuration from those with a cis configuration. It has been shown that the hydrogen atom at C-4 lying on the same side of the amine group at C-5 always resonates at lower field than the hydrogen atom on the opposite side. This rule can be applied for identifying the configuration of the 5-amino-v-triazolines.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 9 (1977), S. 607-608 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The J(23)cis and J(23)trans values in several 2-carbonyl substituted 2,3-dihydrobenzofurans were measured. Although J(cis)〉J(trans), the values found disagree with the Karplus rule.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 13 (1978), S. 319-324 
    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 a series of 4,5-dihydroimidazole derivatives were determined. Deuterium labelling and high resolution mass spectrometry were utilized in order to elucidate the mechanism of a number of fragmentations. The most significant ions arise from the following processes: (1) elimination of the C-4 substituent; (2) cleavage of the 1,2-N—C and 4,5-C—C bonds with or without hydrogen migration; (3) cleavage of the 1,5-N—C and 2,3-C—N bonds with charge retention on the N-1—C-2 moiety.In this paper the standard numbering of the imidazole ring (see structures) is retained for the fragment ions. Anomalous behaviour is shown by the t-butoxy derivative; the reasons for this behaviour are discussed.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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