Abstract
The mechanism of the reaction of N-aminoethyleneimine with some aliphatic aldehydes and with acrolein have been studied. It has been shown that the reaction takes place at the carbonyl bond C=O with the formation of hydrazones.
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S. A. Hiller, A. V. Eremeev, M. Yu. Lidak, and V. A. Pestunovich, KhGS [Chemistry of Heterocyclic Compounds], 4, 819, 1968.
S. A. Hiller and M. Yu. Lidak, Abstracts of Reports to Symposium on the Chemistry of Antitumoral Agents [in Russian], Medgiz, Moscow, 1960.
M. Yu. Lidak, S. A. Hiller, Izv. AN LatvSSR, no. 5, 99, 1961.
A. Dornow and W. Schacht, Ber., 82, 464, 1949.
S. A. Hiller, A. V. Eremeev, M. Yu. Lidak, and V. A. Pestunovich, KhGS [Chemistry of Heterocyclic Compounds], 4, 815, 1968.
A. I. Kost, ZhOKh, 26, 1717, 1956.
B. V. Ioffe and A. Kochetkov, Tetrah. Lett., 11, 1333, 1968.
B. V. Ioffe and K. N. Zelenin, DAN, 144, 1303, 1962.
B. V. Ioffe and K. N. Zelenin, ZhOKh, 32, 1108, 1962.
B. V. Ioffe and K. N. Zelenin, DAN, 134, 1094, 1960.
B. V. Ioffe and K. N. Zelenin, ZhOKh, 32, 481, 1962.
I. I. Grandberg, ZhOKh, 34, 569, 1964.
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For part II, see [1].
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Hiller, S.A., Eremeev, A.V. & Lidak, M.Y. Chemistry of ethyleneimine. Chem Heterocycl Compd 6, 1–5 (1970). https://doi.org/10.1007/BF00475411
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DOI: https://doi.org/10.1007/BF00475411