Abstract
By reactions of α,ω-diamines with 1,2-dihaloethanes there were synthesized α,ω-bis-N-aziridinoalkanes (la-g) and bis-N-aziridinoethyl ether (II). From 1,3-diaminopropane and dichloroethane bis-aziridine (III) was isolated in addition to (Ia). NMR spectra of the products were studied.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature cited
O. C. Dermer and G. E. Ham, Ethylenimine and Other Aziridines, Academic Press, New York (1969), p. 415.
M. M. Crystal, J. Med. Entomol.,9, No. 6, 14509 (1972); Chem. Abstr.,78, 120199d (1973).
M. M. Crystal, Environ. Entomol.,2, No. 1, 145 (1973); Chem. Abstrs.,78, 132659s (1973).
G. Sacca and M. L. Mastrilli, Pierdominice. E. Wiad Parazytol.,18, 655 (1972); Chem. Abstrs.,78, 155403t (1973).
G. Szeimies, Chem. Ber.,106, 3695 (1973).
D. S. Breslow, Ger. Offen 2,163,623. Chem. Abstrs.,78, 4961x (1973).
K. D. Gundermann, K. Burzin, F. J. Sprenger, and H. Schulze, Chem. Ber.,105, 312 (1972).
R. G. Kostyanovskii and O. A. Pan'shin, Izv. Akad. Nauk SSSR, Ser. Khim., No. 3, 567 (1965).
H. Uelzmann, US Patent 3,977,923, Chem. Abstrs.,86, No. 4, 19157d (1977).
V. S. Borisenko, V. K. Krotova, V. A. Bobylev, et al., Inventor's Certificate No. 1,177,297 (USSR), Byull. Izobret., No. 33 (1985).
H. Bestian, Leibigs Ann. Chem.,566, 210 (1950).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 882–885, April, 1991.
Rights and permissions
About this article
Cite this article
Kadorkina, G.K., Mkhitaryan, A.G., Polyakov, A.E. et al. α,ω-Bis-N-aziridinoalkanes. Russ Chem Bull 40, 780–783 (1991). https://doi.org/10.1007/BF00958573
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00958573