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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 2001-2001 
    ISSN: 1434-193X
    Keywords: Addition reactions ; Octahydroacridine ; Polypyridines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A new octahydroacridine with a tert-butoxypropyl group in the 9-position was prepared and was used in the synthesis of new soluble annelated polypyridines. Quinquepyridine with 11 adjacent rings was prepared in 17-25% yield by condensation of an α-methylene ketone and an enolisable ketone in the presence of ammonium acetate under basic conditions.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 987-994 
    ISSN: 1434-193X
    Keywords: Addition reactions ; Octahydroacridine ; Polypyridines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A new octahydroacridine with a tert-butoxypropyl group in the 9-position was prepared and was used in the synthesis of new soluble annelated polypyridines. Quinquepyridine with 11 adjacent rings was prepared in 17-25% yield by condensation of an α-methylene ketone and an enolisable ketone in the presence of ammonium acetate under basic conditions.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2485-2490 
    ISSN: 1434-193X
    Keywords: Molecular recognition ; Host-guest chemistry ; Polypyridines ; Condensation reactions ; Michael additions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Highly soluble annelated bi- and terpyridines were prepared in 46-60% yields by a two-step procedure which combines the Michael addition of an enolizable cyclic ketone with an α,β-unsaturated ketone and the cyclization of the resulting 1,5-diketone in the presence of ammonium acetate.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 2907-2912 
    ISSN: 1434-193X
    Keywords: Polyaza heterocycles ; Enaminones ; Pyrimidines ; Carboxamidines ; Guanidines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple and efficient method for the synthesis of larger polyaza heterocyclic structures 6a, 6b and 8 with 1,3-pyrimidine units has been developed, based on the reaction of enaminones with appropriate guanidines or carboxamidines under basic conditions. Using this procedure, several new, optically active polyaza heterocycles 10, 12 and 13 have been prepared in good yields, from enantiomerically pure Nα-Boc-L-arginine as guanidine reagents.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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