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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 1155-1160 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Chemical shifts ; Revised assignment ; Deuterium isotope effect ; 2-(Bromomethyl)naphthalene ; Bis(bromomethyl)naphthalenes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The assignments of the 13C NMR signals of 2-(bromomethyl)naphthalene (1) were derived by comparison of its spectrum with those of the α,α-D2 and 1-D derivatives, by determination of relative spin-lattice relaxation rates and by inspection of the 13C,1H spin coupling patterns. Literature assignments of 1 and of 2-(bromomethyl)-6-methylnaphthalene are corrected. The procedure by which these assignments has been obtained is critically evaluated. Very good additivity of substituent effects on chemical shifts is observed in the 13C NMR spectra of 2,6- and 2,7-bis(bromomethyl)naphthalene.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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