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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 15 (1981), S. 37-42 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The olefins Ph2P(X)CH=CHR [X=lone pair, O, S, Ch3I; R=Ch3, ph, P(X)ph2] have been prepared and their 1H, 13C and 31P NMR spectra measured. trans 3J[P(IV)C] (range 18.3-25.7 Hz) is greater than cis 3J[P(IV)C] (range 6.9-11 Hz) but this relationship does not hold for P(III) compounds. In the 31P spectra the E isomer absorbs to higher field than the Z isomer for P(III) and P(IV) compounds. The 1H data are in accord with previous results; average substituent shielding coefficients for ph2P(X) substituted alkenes are reported.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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