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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 13 (1980), S. 313-318 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformation of some 2-σ-1,3,2-dioxaphospholanes (σ=OAlkyl, CI) is studied. The determination of the 2J(POC) and 3J(POCC) coupling constants, which are influenced by the bulk of the alkoxy group, is a means of obtaining information about the rotation around the P—OR bond, which is dependent on steric interactions between the phosphorus lone pair, the alkoxy group and the substituents on the ring. When σ is a tert-butoxy group, a direct ‘through-space’ interaction is found between the phosphorus atom and one of the primary carbons of the OR group. If there is no substituent on the ring, the 31P chemical shifts are little affected by changes in OR; a diamagnetic effect is observed, however, in the case of the tert-butoxy group which is enhanced for the 4,4,5,5-tetramethyl derivatives.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 13 (1980), S. 235-239 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Measurements of the 13C chemical shifts of 2-alkoxy-1,3,2-dioxaphospholanes have allowed the determination of the contribution of the substituent to the α-, β- and γ-carbon chemical shifts of attached alkyl groups. The preliminary assignments of the signals were made using the following information; relative intensities, variations in coupling constants J(31P13C) and the existence of linear correlations between the shifts of carbon atoms in the P-alkoxy groups and the degree of substitution of the observed carbon or of its neighbours.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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