Abstract
Under the influence of bases, the 4-6-dimethyl-5-nitro-2-chloro-3-cyanopyridine molecule was found to undergo autohetarylation with the formation of a doubled molecule. Based on RSA data, it was found that such a process takes place exclusively at the methyl group in the 4 position.
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Additional information
M. V. Lomonosov Moscow State University, Moscow 119899. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 680–684, May, 1996.
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Yurovskaya, M.A., Mit'kin, O.D. & Nesterov, V.N. Autohetarylation of 4,6-dimethyl-5-nitro-2chloro-3-cyanopyridine — An unexpected transformation in the presence of bases. Chem Heterocycl Compd 32, 585–589 (1996). https://doi.org/10.1007/BF01164791
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DOI: https://doi.org/10.1007/BF01164791