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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 30 (1992), S. 1117-1121 
    ISSN: 0749-1581
    Keywords: Pyrazolo[1,5-a]pyrimidines ; Structure determination ; Coupling constants ; 1H, 13C and 15N NMR spectra ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The condensation of 3(5)-aminopyrazole and 5-amino-3-phenylpyrazole with ethyl 2,4-dioxopentanoate and 2-ethoxymethylidene-3-oxobutyrate has been re-investigated. Contrary to previos reports, the former reaction gives rise to both regioisomeric pyrazolo [1,5-a]pyrimidines (5-carbethoxy-7-methyl-and 7-carbethoxy-5-methyl-), the structures of which were determined by 1H and 13C NMR spectroscopy. The 6-carbethoxy-7-methyl-regioisomer is shown to be the only product in the reaction of the same aminopyrazoles with 2-ethoxymethylidene-3-oxobutyrate; the regiochemical assignment was independently achieved by multimuclear (13C and 15N) NMR spectroscopy.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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