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Electrophilic reactions of 3-hydroxyisonicotinic acid
Authors:L. D. Smirnov  L. G. Stolyarova  L. V. Shirokova  V. P. Lezina
Affiliation:(1) Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow
Abstract:Conclusions The aminomethylation, azo-coupling, and nitration of 3-hydroxyisonicotinic acid and its ester are directed to the 2 position, whereas their iodination proceeds with the formation of the 2-iodo and 2,6-diiodo derivatives.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 452–454, February, 1977.
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