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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3149-3174 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pteridines, LVII. Syntheses and Properties of Lumazine N-OxidesThe synthesis of lumazine N-oxides via H2O2-oxidation is described. The lumazine system reacts preferentially to N-8-oxides (23-30) if N-1- and crowding C-7-substituents are missing. The reaction path will be controlled by their sterical influence giving raise to the formation of N-5-monoxides (31-43). N-1-Unsubstituted lumazine derivatives form on further oxidation 5,8-di-N-oxides (44-47). The structures are discussed on the basis of pKa-values, u. v. and n. m. r. spectra. Rearrangement reactions by acetic anhydride to 6- and 7-hydroxylumazines proceeded successfully.
    Notes: Die Synthese von Lumazin-N-oxiden durch H2O2-Oxidation wird beschrieben. Das Lumazinsystem reagiert bevorzugt zu N-8-Oxiden (23-30), sofern N-1- und raumerfüllende C-7-Substituenten fehlen. Ihr sterischer Einfluß ist so groß, daß in diesen Fällen ausschließlich N-5-Monoxide (31-43) gebildet werden. Bei unsubstituierter N-1-Position führt Weiteroxidation zu 5,8-Di-N-oxiden (44-47). Die Konstitutionen werden auf der Basis von pKa,-Werten, UV- und NMR-Spektren diskutiert. Umlagerungsreaktionen mit Acetanhydrid zu 6- bzw. 7-Hydroxylumazinen wurden durchgeführt.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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