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  • 1990-1994  (1)
  • 1985-1989  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 30 (1992), S. 768-773 
    ISSN: 0749-1581
    Keywords: Brucine Gibberellic acid ; Gradient-selective COSY 2D correlation ; Double-quantum filter ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High-quality gradient-selective COSY spectra were recorded at 300 MHz for brucine and gibberellic acid and double-quantum filtered gradient-selective COSY spectra for brucine, using a single-frequency, high-resolution 1H probe modified by the addition of an unshielded z-gradient coil set. Data were efficiently recorded using buffered acquisition with a single transient per increment in 1t, in times much lower than those required for phase-cycled COSY, and with no loss of information. Gradient-selective COSY90, COSY45 and long-range COSY45 experiments, and the correlations leading to chemical shift assignments for gibberellic acid, are reported.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 23 (1985), S. 259-262 
    ISSN: 0749-1581
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Consistently deshielding 13C δ shifts resulting from the presence of aryl ortho substituents have been measured for the 3-methylene carbon atoms of some N-aryl-1-isoindolinones (0.12-3.25 ppm) and for the carbonyl carbon atoms of these compounds and corresponding N-arylisoindoline-1,3-diones (0.04-1.47 ppm). Low-temperature (-75 and -150 °C) 1H NMR studies indicate that steric barriers to internal rotation about the aryl C—N bonds in the N-aryl-1-isoindolinones are low. The compounds with the bulkiest aryl ortho substituents tend to show the largest δ shifts (particularly for the 3-methylene carbons). No consistent correlation with the size of aryl ortho-substituents or their expected electronic properties is evident.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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