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  • 1
    Electronic Resource
    Electronic Resource
    The Sommelet Reaction (1948)
    [s.l.] : Nature Publishing Group
    Nature 161 (1948), S. 723-724 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] IN 1913 Sommelet1 observed that when the quaternary compound from benzyl chloride and hexamine is heated in water, or in aqueous alcohol, it is converted in good yield to benzaldehyde. This reaction has become general for the preparation of aromatic aldehydes. Sommelet isolated ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/161723b0
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Occurrence of Configurational Inversion during Tritiation by the Wilzbach Method (1963)
    [s.l.] : Nature Publishing Group
    Nature 197 (1963), S. 485-486 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] We have chosen (-)-inositol (I) for an investigation of the stereochemistry of Wilzbach labelling, because in this compound replacement of any hydrogen atom attached to carbon by tritium with inversion will result in the formation of a different isomer: myo- (II), allo- (III), or muco-inositol ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/197485a0
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  • 3
    Electronic Resource
    Electronic Resource
    Specific Tritium Labelling by the Wilzbach Method (1964)
    [s.l.] : Nature Publishing Group
    Nature 202 (1964), S. 176-177 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The myoinositol (specific activity 1-29 c./mole) was converted into its c?/cZahexylidene derivative* (spec. act. 1*30 c./mole); because myoinositol is symmetrical, equal amounts of 1,2-0- and 2,3-0-c^cZohexyUdenemyoinositol are obtained. Oxidation with sodium periodate yielded the ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/202176a0
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