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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 44 (1961), S. 762-770 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two types of 2,6-dimethyl-benzo[1,2,4,5]bis-imidazole-4,8-quinones (X, R = H and R = C6H5) are known. The method of EFROS6) (X, R = H) is unsuitable for the synthesis of N-substituted benzo-bis-imidazole-quinones, whilst the ring closure of FRIES and REIZ3) proceeds with low yield and works only with N-aryl compounds. A new convenient synthesis for hydroquinones of type IX and quinones of type X has been found: the tetraaminoquinones II are reduced to the hydroquinones VIII; subsequent cyclisation with acids leads to the new benzo-bis-imidazole hydroquinones IX, which on oxidation are converted to the quinones X.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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