Summary
The nitrosylation of 2,4,6-trisubstituted phenols takes place only in the para-position and, depending on the nature of the substituents, leads to substitutional nitration or to the formation of nitroquinolide compounds.
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The authors would like to express their gratitude to N. M. Émanuél' for his constant interest in this work during its performance.
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya No. 11, pp. 2082–2084, November, 1964
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Ershov, V.V., Zlobina, G.A. Electrophilic interaction of nitrous acid with 2,4,6-trisubstituted phenols. Russ Chem Bull 13, 1980–1982 (1964). https://doi.org/10.1007/BF00844498
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DOI: https://doi.org/10.1007/BF00844498