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Chemistry of Heterocyclic Compounds

, Volume 31, Issue 5, pp 615–620 | Cite as

Electrophilic substitution in benzo[b]furo[2,3-c]pyridines: nitration, acylation

  • S. V. Tolkunov
  • M. N. Kal'nitskii
  • V. I. Dulenko
  • S. N. Lyashchuk
Article
  • 30 Downloads

Abstract

It has been shown that the nitration and acylation of substituted benzo[b]furo[2,3-c]pyridines proceeds exclusively at position 6 of the benzene ring. If position 6 is blocked by a substitutnt, the product of monosubstitution at the C(8) atom is formed. The molecules that were investigated have been calculated in the MNDO approximation.

Keywords

Benzene Organic Chemistry Pyridine Benzene Ring Nitration 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    S. V. Tolkunov, M. N. Kal'nitskii, and V. I. Dulenko, Khim. Geterotsikl. Soedin., No. 5, 706 (1993).Google Scholar
  2. 2.
    S. V. Tolkunov, M. N. Kal'nitskii, S. N. Lyashchuk, and V. L Dulenko, Khim. Geterotsikl. Soedin., No. 5, 701 (1994).Google Scholar
  3. 3.
    V. I. Dulenko and S. V. Tolkunov, Khim. Geterotsikl. Soedin., No. 7. 889 (1987).Google Scholar
  4. 4.
    M. J. S. Dewar and W. Thiel, J. Am. Chem. Soc.,99, 4899 (1977).Google Scholar
  5. 5.
    Serena Software, P. O. Box 3076, Bloomington, IN.Google Scholar

Copyright information

© Plenum Publishing Corporation 1995

Authors and Affiliations

  • S. V. Tolkunov
  • M. N. Kal'nitskii
  • V. I. Dulenko
  • S. N. Lyashchuk

There are no affiliations available

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