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Two directions of interaction of 2-aryl-1,2,3,4-tetrahydropyridine-3,3,4,4-tetracarbonitriles with nucleophiles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Depending on the reaction conditions, 2-aryl-1,2,3,4-tetrahydropyridine-3,3,4,4-tetracarbonitriles react with alcohols, thiols and ketoximes to give 3-amino-4-aryl-1,1-di[R-oxy(thio)]-6,7-dialkyl-3a,4,5,7a-tetrahydro-1H-pyrrolo[3,4-c]pyridine-3a, 7a-dicarbonitrles or 2-aryl-5,6-dialkylpyridine-3,4-dicarbonitriles.

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References

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Authors
  1. Ya. S. Kayukov
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  2. O. E. Nasakin
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  3. Ya. G. Urman
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  4. V. N. Khrustalev
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  5. V. N. Nesterov
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  6. M. Yu. Antipin
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  7. A. N. Lyshchikov
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  8. P. M. Lukin
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Additional information

Chuvash State University, Cheboksary 428015. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 367–375, March, 1997.

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Kayukov, Y.S., Nasakin, O.E., Urman, Y.G. et al. Two directions of interaction of 2-aryl-1,2,3,4-tetrahydropyridine-3,3,4,4-tetracarbonitriles with nucleophiles. Chem Heterocycl Compd 33, 310–317 (1997). https://doi.org/10.1007/BF02253111

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  • DOI: https://doi.org/10.1007/BF02253111

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