The reaction of (hetero)aromatic aldehydes, cyanoselenoacetamide, and 1-(cyanoacetyl)-3,5-dimethyl-pyrazole in the presence of triethylamine gives a mixture of the cis and trans diastereomers of triethylammonium 4-aryl(hetaryl)-3,5-dicyano-6-oxo-1,4,5,6-tetrahydropyridine-2-selenolates. The selenolates obtained react with alkyl halides to form the corresponding selenides.
Similar content being viewed by others
References
V. P. Litvinov and V. D. Dyachenko, Usp, Khim,, 66, 1025 (1997).
V. P. Litvinov, Izv. Akad. Nauk, Ser. Khim., 2123 (1998).
S. G. Krivokolysko, Diss. Cand. Chem. Sci., Moscow (1997).
V. D. Dyachenko, Diss. Doct. Chem. Sci., Moscow (1998).
V. D. Dyachenko, A. E. Mitroshin, and V. P. Litvinov, Khim. Geterotsikl. Soedin., 1235 (1996). [Chem. Heterocycl. Compd., 32, 1058 (1996)].
V. V. Dotsenko, S. G. Krivokolysko, and V. P. Litvinov, Izv. Akad. Nauk, Ser. Khim., 2397 (2007).
V. V. Dotsenko, S. G. Krivokolysko, and V. P. Litvinov, Monatsh. Chem., 138, 607 (2007).
S. G. Krivokolysko, V. D. Dyachenko, E. B. Rusanov, and V. P. Litvinov, Khim. Geterotsikl. Soedin., 525 (2001). [Chem. Heterocycl. Compd., 37, 477 (2001)].
K. A. Frolov, V. V. Dotsenko, S. G. Krivokolysko, and V. P. Litvinov, Khim. Geterotsikl. Soedin., 1413 (2010). [Chem. Heterocycl. Comp., 46, 1142 (2010)].
S. G. Krivokolysko, Diss. Doct. Chem. Sci., Moscow (2001).
V. D. Dyachenko, E. B. Rusanov, V. P. Litvinov, and A. V. Turov, Ukr. Khim. Zh. 56, 408 (1990).
V. P. Litvinov, V. Yu. Mortikov, Yu. A. Sharanin, and A. M. Shestapolov, Synthesis, 98 (1985).
Author information
Authors and Affiliations
Corresponding author
Additional information
V. P. Litvinov (Deceased).
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 471-477, March, 2012.
Rights and permissions
About this article
Cite this article
Frolov, K.A., Dotsenko, V.V., Krivokolysko, S.G. et al. Synthesis and properties of triethylammonium 4-aryl(hetaryl)-3,5-dicyano-6-oxo-1,4,5,6-tetrahydro-pyridine-2-selenolates. Chem Heterocycl Comp 48, 442–447 (2012). https://doi.org/10.1007/s10593-012-1012-4
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10593-012-1012-4