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  • 1975-1979  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 60 (1977), S. 1501-1509 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 15N-Chemical shifts of 32 enamines, 11 enaminoketones and 28 closely related amines have been determined with the isotope in natural abundance. In order to eliminate substituent effects, differential chemical shifts Δδ(N) are defined as δN(amine)-δN(enamine). This parameter is shown to correlate well with the free enthalpy of activation ΔG# for restricted rotation about the N—C(α) bond in enamines with extended conjugation. Δδ(N) values of substituted anilinostyrenes correlate also with 13C-chemical shifts of the β-carbon in the enamine system and with Hammett σ-constants of the aniline substituents. The experimental results suggest that differential 15N shifts are a useful probe to study n, π-interaction in enamines.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 15N-Chemical shifts of a series of 5, 6, 7, 8-tetrahydropterins, 7, 8-dihydropterins and pterins have been measured in acidic solution by means of a probe for 20 mm sample tubes. Included are the relevant data of folic acid (11), 5, 6, 7, 8-tetrahydrofolic acid (5) and N (5, 10)-metheno-5, 6, 7, 8-tetrahydrofolic acid (6). The different oxidation states are clearly relected in the chemical shifts of N (5) and N (8). Assignment of the nitrogen resonances was achieved by protonation effects (discrimination between N (1) and N (3)) and with the aid of alkyl substitution at C (6) and C(7), to distinguish between N (5) and N (8).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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