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Chemistry of Heterocyclic Compounds

, Volume 28, Issue 11, pp 1255–1259 | Cite as

Reactions of 3,3,4,4-tetracyanopyrrolidines with alcohols

  • O. E. Nasakin
  • A. N. Lyshchikov
  • P. M. Lukin
  • V. A. Tafeenko
Article

Abstract

It was established that on treatment with alkali, 2,5-disubstituted 3,3,4,4-tetracyanopyrrolidines react with primary alcohols to form 5-alkoxy-2-(N-arylidenamino)-3,4-dicyanopyrroles. Depending on the ratio of the initial reagents, another reaction route is possible, leading to 6-alkoxy-4-amino-2-R-3-CH2R-5-cyano-3H-pyrrolo[2,3-d]pyrimidines. The effect of substituents on the reaction pathways is examined.

Keywords

Alcohol Organic Chemistry Pyrimidine Reaction Pathway Primary Alcohol 
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

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Copyright information

© Plenum Publishing Corporation 1993

Authors and Affiliations

  • O. E. Nasakin
    • 1
  • A. N. Lyshchikov
    • 1
  • P. M. Lukin
    • 1
  • V. A. Tafeenko
    • 1
  1. 1.Chuvash State UniversityCheboksary

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