Autohetarylation of 4,6-dimethyl-5-nitro-2-chloro-3-cyanopyridine — An unexpected transformation in the presence of bases

Authors

  • M. А. Юровская M. V. Lomonosov Moscow State University, Moscow 119899
  • О. Д. Митькин M. V. Lomonosov Moscow State University, Moscow 119899
  • B. Н. Нестеров M. V. Lomonosov Moscow State University, Moscow 119899

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.

How to Cite
Yurovskaya, M. A.; Mit'kin, O. D.; Nesterov, V. N. Chem. Heterocycl. Compd. 1996, 32, 585. [Khim. Geterotsikl. Soedin. 1996, 680.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01164791

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Published

1996-05-25

Issue

No. 5 (1996)

Section

Original Papers