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  • 2000-2004  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 543-548 
    ISSN: 1434-193X
    Keywords: Supramolecular chemistry ; Domino reactions ; Oligopyridines ; Dihydropyridines ; Mannich bases ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---An annelation reaction is presented in which 1,3-cyclohexanedione (1) and Mannich bases 6a,b are used for the preparation of functionalized bipyridines 12a, 13a, 14a and dihydropyridine derivatives 10b, 11b. All these products possess a keto group which will allow further transformations. The same concept was applied for the synthesis of the S-shaped terpyridine 25. The reaction of the Mannich base 21 with 1,3-cyclohexanedione yielded the heptacyclic terpyridine 22, which is a key intermediate for the synthesis of torands and other tridentate clefts. The ketone 12a was used for the synthesis of the quaterpyridine 26.
    Type of Medium: Electronic Resource
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