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  • Analytical Chemistry and Spectroscopy  (2)
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  • Analytical Chemistry and Spectroscopy  (2)
  • Chemistry  (2)
  • 1
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The configuration of isomeric 3,3-dimethyl-1-phenyl-1,3-dihydrobenzo[c]thiophene 2-oxides was assigned on the basis of selective benzene- and TFA-induced NMR shifts. The same method was employed for assigning the α-methyl resonances of these sulphoxides. Examination of NMR data for a variety of cyclic sulphoxides revealed that in CCl4 or CDCl3 solution, α-hydrogen cis to S—O often resonates at higher magnetic field, while α-methyl group cis to S—O characteristically resonates at lower field, than the same hydrogen or methyl group trans to S—O, respectively.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 3 (1971), S. 429-432 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The methylene protons of dibenzyl sulphoxide are magnetically equivalent in low dielectric and non-equivalent in high dielectric constant solvents, while for diphenacyl sulphoxide this behaviour is reversed. In both cases, the variation in the magnitude of the non-equivalence reflects a greater downfield shift of one methylene proton than the other on passing from non-polar to polar solvents. By contrast, the chemical shift difference between the benzyl methylene protons or between the phenacyl methylene protons of benzyl phenacyl sulphoxide varies only slightly with solvent polarity.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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