Abstract
The reaction of 1,1,2,2-tetracyanoethane with 1-R,3-R,5-R-2,4-diazapenta-1, 4-dienes leads to 2,5-disubstituted 3,3,4,4-tetracyanopyrrolidines. The conditions for the acylation of the last were selected.
Similar content being viewed by others
References
O. E. Nasakin, V. V. Alekseev, V. K. Promonenkov, Yu. P. Belov, A. Kh. Bulai, and S. Yu. Sii'vestrova, Khim. Geterotsikl. Soedin., No. 3, 402 (1981).
O. E. Nasakin, V. V. Alekseev, P. B. Terent'ev, A. Kh. Bulai, and M. Yu. Zabolotskaya, Khim. Geterotsikl. Soedin., No. 8, 1062 (1983).
USSR A. S. 1178746; O. E. Nasakin, M. P. Vorob'eva, I. A. Abramov, L. S. Shevnitsyn, A. Ya. Chernikhov, M. N. Yakovlev, A. V. Sukhobokov, and L. A. Alekseeva, Byull. Izobret., No. 34 (1985).
O. E. Nasakin, V. V. Alekseev, P. B. Terent'ev, A. Kh. Bulai, and M. Yu. Zabolotskaya, Khim. Geterotsikl. Soedin., No. 8, 1067 (1983).
Ya. L. Gol'dfarb, E. G. Ostapenko, and V. G. Vinogradova, Khim. Geterotsikl. Soedin., No. 7, 902 (1987).
A. Galfe, Chim. Ind.,93, 259 (1965).
A. B. Zolotoi, A. N. Lyshchikov, P. M. Lukin, A. I. Prokhorov, O. E. Nasakin, A. Kh. Bulai, and L. O. Atovmyan, Dokl. Akad. Nauk,313, 110 (1990).
A. I. Prokhorov, A. B. Zolotoi, A. N. Lyshchikov, P. M. Lukin, O. E. Nasakin, and L. O. Atovmyan, Zh. Strukt. Khim.,32, 108 (1991).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 353–358, March, 1994.
Rights and permissions
About this article
Cite this article
Nasakin, O.E., Lyshchikov, A.N., Lukin, P.M. et al. Synthesis of 2,5-distributed 3,3,4,4-tetracyanopyrrolidines. Chem Heterocycl Compd 30, 312–316 (1994). https://doi.org/10.1007/BF01165697
Issue Date:
DOI: https://doi.org/10.1007/BF01165697