1969 年 17 巻 4 号 p. 763-769
NMR spectra of 3-hydroxypyridazine 1-oxides and their monomethylated derivatives were examined and structural propriety of their nitrated and halogenated products was confirmed by the analyses of the NMR spectra. Furthermore, in 3-hydroxypyridazine 1-oxides, predominance of enol form tautomer was proved by NMR data. The conclusion was also drawn by other spectral data (UV and IR).