Author:
Hansen John F.,Luther Matthew L.
Reference12 articles.
1. Nitrosation of .alpha.,.beta.-unsaturated oximes. V. Synthesis and chemistry of 1-hydroxypyrazole 2-oxides
2. Nitrosation of .alpha.,.beta.-unsaturated oximes. IV. Synthesis and structure of 3,4-diazacyclopentadienone derivatives
3. Isolation of a new 1-hydroxypyrazole 2-oxide via chelation
4. Preparation and oxidation of 1-hydroxypyrazoles and 1-hydroxypyrazole 2-oxides
5. In 1-hydroxypyrazole 2-oxide a situation exists which is similar to that in N-unsubstituted pyrazoles, namely that the C3 and C5 positions of the ring are indistinguishable due to the chelation of the acidic proton with both oxygens or to rapid exchange between them. This ambiguity in numbering is indicated by showing the alternative numbering in parentheses, C3(5) or C5(3).
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