Abstract
A method is worked out for synthesizing N, N′-diazirydinylsulfide, -disulfide, -sulfoxide, -sulfone, from ethyleneimine and, respectively, SCl2, S2Cl2, SOCl2, and SO2CL2 [1]. A study is made of these compounds, their IR spectra, and their complexes with picric acid and mercury salts.
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M. G. Voronkov, L. A. Fedotova, and D. O. Rinkis, Author's Certificate, File No. 870268/23-4, 1963.
A. Michaelis, Ber., 28, 1012, 1895.
A. Michaelis and K. Luxemburg, Ber., 28, 165, 1895.
F. Lengfeld and J. Stieglitz, Ber., 28, 575, 1895.
P. C. Jones, U. S. Patent 2259 164, 1941; C.A., 36, 498, 1942.
J. A. Lambrecht, W. H. Hensley, and R. E. Kent, U.S. Patent, 2902402 1959; C. A., 54, 5716, 1960.
R. P. Louthan and C. W. Kruse, U.S. Patent 2 886 593, 1959; C. A., 54, 18066, 1960.
R. P. Louthan, U.S. Patent 2927131, 1960; C. A., 54, 15245, 1960.
H. Jenne and M. Becke-Goehring, Ber., 91, 1950, 1958.
C. Howard and W. Markwald, Ber., 32, 2036, 1899.
Kuo Tu-jên and L. S. Efros, ZhOKh, 33, 966, 1963.
A. W. Craig, H. Jacson, and R. M. V. James, Brit. J. Pharmacol., 21, 590, 1963.
Yu. N. Sheinker, E. M. Peresleni, and G. I. Braz, ZhFKh, 29, 518, 1955.
Handbook of Preparative Inorganic Chemistry ed. G. Brauer [Russian translation], IL, Moscow, 192, 193, 1956.
M. Lidak, Ya. Litsis, and A. Veiss, Izv. AN LatvSSR, no. 2, 101, 1960.
M. O. Korshun, N. E. Gel'man, and N. S. Sheveleva, ZhAKh, 13, 695, 1958.
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We wish to thank V. E. Egerta and I. L. Priedite for carrying out the C, H, N, and S analyses, and A. K. Grinvalde for determining the IR spectra.
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Voronkov, M.G., Fedotova, L.A. & Rinkis, D.O. Heteroatom derivatives of aziridine. Chem Heterocycl Compd 1, 488–491 (1965). https://doi.org/10.1007/BF00469924
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DOI: https://doi.org/10.1007/BF00469924