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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2664-2667 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-(Alkylamino)-4-(dichloromethyl)quinolines from (Trichlorovinyl)ketene N-Arylimines and Aliphatic AminesOn treatment of the N-alkylketene imine 2a with morpholine in THF, the amino substituted butenimine 5a is formed probably via 3a. When, however, the N-arylketene imines 2b and c, generated in situ from the amides 4b and c, react with secondary aliphatic amines or tert-butylamine the quinolines 6a-c are produced. The structure of 6b is confirmed by the 13C NMR spectrum. The formation of 5a and quinolines 6 from 2 may be considered as an evidence for compounds of type 3 and 5 as intermediates in the formation of 7 from 1 or 2 with primary amines (see preceding paper).
    Type of Medium: Electronic Resource
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