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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1295-1303 
    ISSN: 0009-2940
    Keywords: Imines ; Iminium salts ; 3-Trifloxypropeniminium salts ; Propyniminium salts ; Cyclization reactions ; Azacyclobutadiene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The imines 5 and 11 react with 3-trifloxypropeniminium triflates 1a-d to afford the heterocyclic iminium salts 8, 9, 13, 15, and 17, respectively, or the propeniminium salt 21. Propyniminium triflates 22, 24 react with imines by initial conjugated addition, followed by a reaction sequence analogous to the one observed for the reactions of 1a-d with imines. Thus, salt 22 and aldimine 5b yield the propeniminium salt 21, while 24 reacts with tri-tert-butylazete 25 to afford the semicyclic vinamidinium salt 28. A crystal structure analysis of 28 is performed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1994 (1994), S. 429-432 
    ISSN: 0170-2041
    Keywords: Iminium salts, semicyclic ; Propyniminium salts ; Trifluoromethanesulfonic anhydride ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: O-Sulfonylation of 2-oxomethylene-substituted 1-azaheterocycles 1 yields the 3-trifloxypropeniminium triflates 2a-e in high yield. Thermal β-elimination of triflic acid from these salts affords the propyniminium triflates (2-ethynylcycliminium triflates) 3a-e. The treatment of semicyclic enamino ketones 1f, g with triflic anhydride yields directly the propyniminium triflates 3f, g.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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