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  • 1
    ISSN: 1573-9171
    Keywords: azoles ; O-fluorosulfonyl-N ; N-difluorohydroxylamine ; phasetransfer catalysis ; N-fluorosulfonylazoles ; N ; N-fluorosulfonylbisazoles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract O-Fluorosulfonyl-N,N-difluorohydroxylamine (FH) reacts with anions of NH-azoles (imidazoles, pyrazoles, and 1,2,3-triazoles) to give the corresponding N-fluorosulfonylazoles, which were used to obtain N,N′-sulfonylbisazoles. The N-fluorosulfonylation proceeds at the nitrogen atom furthest from the most electron-withdrawing substituent in the azole ring..Nonaromatic NH-acid anions (imides and primary N-nitroamines) are sometimes capable of giving N-flurosulfonyl derivatives although in yields less than 5%. These products are much less stable than N-fluorosulfonylazoles. The N-fluorosulfonylation presumably proceeds as nucleophilic substitution at the sulfur atom of FH.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 42 (1993), S. 1555-1558 
    ISSN: 1573-9171
    Keywords: 1-nitropyrazole, substituted N-nitropyrazoles ; 13C,14N, and15N NMR ; chemical shifts13C,14N, and15N ; coupling constants $$J_{13_C ,1_H } $$ and $$J_{15_N ,1_H } $$
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The NMR spectra (13C,15N, and14N) of N-nitropyrazoles containing nitro, methyl, and cyano groups in the pyrazole ring were investigated.13C NMR spectra were recorded under conditions of triple selective heteronuclear resonance13C-{1H,14N}. The effect of substituents in the pyrazole ring on the chemical shifts in the13C and15N NMR spectra is discussed. Coupling constants $$J_{13_C ,1_H } $$ and $$J_{15_N ,1_H } $$ obtained by the polarization transfer method [1H]→13C and [1H]→15N (INEPT, SPT) were measured and completely assigned.
    Type of Medium: Electronic Resource
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