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  • 1975-1979  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 895-904 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pyrazolone Derivatives. I. Synthesis, Stereochemistry, and Photochemical Behaviour of Azomethines of 1,5-Dimethyl-2-phenyl-4-formyl-Δ4-pyrazolinone-(3) (Antipyraldehyde)Condensation of Antipyraldehyde with primary amines yielded a series of anils. By 1H-n.m.r.-spectroscopy and 15N-isotope technique is shown that the azomethines exist in the E-configuration. By a photochemical reaction the Z-isomer is produced which could be detected at low temperatures.
    Notes: Durch Kondensation von Antipyrinaldehyd mit primären Aminen wurde eine Reihe Schiffscher Basen erhalten. Mit Hilfe der 1H-NMR-Spektroskopie und der 15N-Isotopentechnik wird nachgewiesen, daß die Azomethine als E-Isomere vorliegen. Das photochemische Verhalten der Anile ist durch eine E-/Z-Isomerisierung an der C=N-Doppelbindung geprägt. Die photochemisch erzeugten Spezies lassen sich bei tiefen Temperaturen nachweisen.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 905-910 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pyrazolone Derivatives. II. Synthesis of Tautomeric Enamines of Some 3-Substituted 1-Phenyl-Δ2-pyrazolinones-(5)By condensation of 3-substituted 4-hydroxymethylene-1-phenyl-Δ2-pyrazolinones-(5) with primary amines stable 4-aminomethylene-Δ2-pyrazolinones-(5) were prepared in high yields. The same derivatives are formed by amine-exchange of 4-N,N-dimethylamino-methylene-Δ2-pyrazolinones-(5). Compared to it, azomethines derived from 5-methoxy-3-methyl-1-phenyl-pyrazole are instable. Such compounds spontaneously form 4-aminomethylene-Δ2-pyrazolinones-(5).
    Notes: Durch Kondensation von 3-substituierten 4-Hydroxymethylen-1-phenyl-Δ2-pyrazolinonen-(5) mit primären Aminen wurden eine beträchtliche Anzahl stabiler 4-Aminomethylen-Δ2-pyrazolinone-(5) in guter Ausbeute erhalten. Die gleichen Reaktionsprodukte entstehen, wenn 4-N, N-Dimethylaminomethylen-Δ2-pyrazolinone-(5) einer Umaminierung unterworfen werden. Dagegen sind Azomethine, die sich vom 5-Methoxy-3-methyl-1-phenyl-pyrazol ableiten, instabil. Es bilden sich spontan die 4-Aminomethylen-Δ2-pyrazolinone-(5).
    Additional Material: 1 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 206-216 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Photochemistry of Sydnonazomethines-(4)Sydnon-4-aldehydes 1-3 react with prim. amines or N-sulfinylanilines to sydnon-azomethines. The i.r.-spectra are discussed. Sydnonazomethines undergo a photoinduced E/Z-isomerisation, at room temperature; a rapid thermic back-reaction (Z/E-isomerisation) takes place, however. The photostationary states at -75°C are analyzed. The rate constants of the thermic back-reaction at 18°C are measured by means of flash-photolysis. The quantum yields for the E/Z-isomerisation (at -75°C) and the photolytic decomposition have the value of 〉0,1 and 〈10-3 respectivly.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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