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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 61 (1909), S. 396-412 
    ISSN: 0863-1778
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1. In ammoniakalischer und in saurer Lösung tritt die Ausscheidung des Schwefelnickels unter geeigneten Bedingungen verspätet ein.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 299-308 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of 2-Cyclopropen-1-yl Azides2-Cyclopropen-1-yl azides (1) react with dimethyl acetylenedicarboxylate (2) to yield 2-(2-cyclopropen-1-yl)-2H-1,2,3-triazoles (7). The reaction of 1 with N,N-diethyl-1-propynylamine (10) give either 2-(2-cyclopropen-1-yl)-2H-1,2,3-triazoles (13) and 3-(2-cyclopropen-1-yl)-3H-azirines (12) or pyridine derivatives (15), depending on the reaction conditions.
    Notes: Aus 2-Cyclopropen-1-yl-aziden 1 und Acetylendicarbonsäure-dimethylester (2) werden 2-(2-Cyclopropen-1-yl)-H2-1,2,3-triazole (7) erhalten. 2-Cyclopropen-1-yl-azide (1) liefern mit N,N-Diethyl-1-propinylamin (10) in Abhängigkeit von den Reaktionsbedingungen entweder 2-(2-Cyclopropen-1-yl)-2H-1,2,3-triazole (13) und 3-(2-Cyclopropen-1-yl)-3H-azirine (12) oder Pyridinderivate (15).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 3695-3703 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1.2.3-Triazines, IThe triaryl-substituted cyclopropenyl azides 3a-k form the triaryl-substituted 1.2.3-triazines 2a-k when heated in dimethylformamide. Diphenylcyclopropenyl azide (31) was rearranged to 4.5-diphenyl-1.2.3-triazine (21).
    Notes: Die triarylsubstituierten Cyclopropenylazide 3a-k bilden beim Erhitzen in Dimethyl-formamid die triarylsubstituierten 1.2.3-Triazine 2a-k. Durch Umlagerung des Diphenyl-cyclopropenylazids (31) wurde das 4.5-Diphenyl-1.2.3-triazin (21) erhalten.
    Additional Material: 3 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 44 (1911), S. 1274-1280 
    ISSN: 0365-9496
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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