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

Authors

  • Я. С. Каюков I. N. Ul'yanov Chuvash State University, Cheboksary 428015
  • O. E. Насакин I. N. Ul'yanov Chuvash State University, Cheboksary 428015
  • Я. Г. Урман I. N. Ul'yanov Chuvash State University, Cheboksary 428015
  • В. Н. Хpустaлев I. N. Ul'yanov Chuvash State University, Cheboksary 428015
  • B. Н. Нестеров I. N. Ul'yanov Chuvash State University, Cheboksary 428015
  • М. Ю. Антипин I. N. Ul'yanov Chuvash State University, Cheboksary 428015
  • А. Н. Лыщиков I. N. Ul'yanov Chuvash State University, Cheboksary 428015
  • П. M. Лукин I. N. Ul'yanov Chuvash State University, Cheboksary 428015

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.

How to Cite
Kayukov, Y. S.; Nasakin, O. E.; Urman, Y. G.; Khrustalev, V. N.; Nesterov, V. N.; Antipin, M. Yu.; Lyshchikov, A. N.; Lukin, P. M. Chem. Heterocycl. Compd. 1997, 33, 310. [Khim. Geterotsikl. Soedin. 1997, 367.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02253111

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Published

2025-10-27

Issue

No. 3 (1997)

Section

Original Papers