Abstract
The reaction of aryl diazonium salts containing electron-withdrawing substituents in the aromatic ring with acetone oxime leads to the formation of nitrogen-containing products instead of the expected functional derivatives of 1-alkyl-3-aryltriazene 1-oxides. The structure of these products is a function of the number and chemical nature of the substituents in the diazo component.
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Additional information
N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 8, pp. 1911–1913, August, 1992.
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Zlotin, S.G., Prokshits, O.V. & Luk'yanov, O.A. Reaction of aryldiazonium salts with acetone oxime. Russ Chem Bull 41, 1495–1496 (1992). https://doi.org/10.1007/BF00864353
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DOI: https://doi.org/10.1007/BF00864353