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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 1691-1698 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Heterocyclizations, XVII. s-Triazolo[1,2-a]-s-triazolesThe title compounds 4 are prepared 1. by cyclocondensation of the urazoles (1,2,4-triazolidine-3,5-diones) 1a-c with isocyanates, 2. by insertion of carbonyle into the 1-carbamoylurazoles 1n-v, using phosgene or N,N′-carbonyldiimidazole (2), 3. by thermolysis of 1a, b, d with 2 in situ. The unsymmetric compound 4f is readily converted into the symmetric 4a via exchange of isocyanate. In contrast, 1a, b react with acyl isothiocyanates to give the 1,3,4-thiadiazolo[3,4-a][1,2,4]-triazoles 3, a novel ring system.
    Notes: Die Titelverbindungen 4 werden 1. durch Cyclokondensation der Urazole (1,2,4-Triazolidin-3,5-dione) 1a-c mit Isocyanaten, 2. durch Carbonyl-Insertion in die 1-Carbamoylurazole 1n-v mittels Phosgen oder N,N′-Carbonyldiimidazol (2), 3. durch Thermolyse von 1a, b, d mit 2 in situ dargestellt. Das unsymmetrische 4f tauscht leicht Isocyanat aus und geht in das symmetrische 4a über. Dagegen reagieren 1a, b mit Acylisothiocyanaten zu den 1,3,4-Thiadiazolo[3,4-a][1,2,4]-triazolen 3, einem neuen Ringsystem.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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