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Oligomers of aziridines and N-β-aziridinoethylamides

  • Organic Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    An efficient method of aziridine dimer synthesis is presented involving reaction of aziridine with esters of strong organic acids followed by alkaline hydrolysis of the resultant N-acyl derivatives.

  2. 2.

    New N-acyl and carbamoyl derivatives of aziridine dimer and trimer were synthesized.

  3. 3.

    Linear and branched isomers of aziridine tetramer and also diastereomers of 2-methylaziridine dimer were isolated and characterized.

  4. 4.

    An efficient regiospecific synthesis of 2,2-dimethylaziridine dimer and trimer was developed.

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Literature cited

  1. Yu. É. Bartoshevich and R. G. Kostyanovskii, Antibiotics (1965), p. 1069; T. V. Sal'nikova, Genetica,5, 39 (1969).

  2. V. N. Syurin and A. E. Lobastov, Problems of Virology, Molecular Biology, and Histology of Agricultural Animals: Collected Scientific Works [in Russian], Izd. Moskovskoi Veterinarnoi Akademii (1963), p. 3; I. K. Rozhdestvenskii, Veterinary Science [in Russian] (1984), p. 61.

  3. O. C. Dermer and G. E. Ham, Ethyleneimine and Other Aziridines, Academic Press, New York (1969), p. 592; H. Bestain, Liebigs Ann. Chem.,566, 210 (1950).

    Google Scholar 

  4. É. I. Budovskii, M. A. Zalesskaya, V. P. Leshchinskaya, and R. G. Kostyanovskii, Bioorg. Khim.,11, 989 (1985); T. B. Tanirbergenov, S. V. Vasil'eva, R. G. Kostyanovskii, et al., Genetika,24, 763 (1988).

    Google Scholar 

  5. P. A. Gembitskii, A. I. Chmarin, and D. S. Zhuk, Khim. Promst., 502 (1972).

  6. J. M. Motes, Patent No. 4,170,591 (USA), Chem. Abstr.,92, 146581 m (1980); V. K. Ukraintsev and Yu. N. Kukushkin, Zh. Obshch. Khim.,56, 1653 (1986).

    Google Scholar 

  7. Dow Chemical Co., Patent No. 2,074,661 (USA), Chem. Abstr.,77, 114230 v (1972).

    Google Scholar 

  8. P. A. Gembitskii, G. A. Tolstikov, L. V. Bokina, et al., Inventor's Certificate 1,177,297 (USSR), Byull. Izobret., No. 33 (1985).

  9. V. N. Andronov, V. A. Aleksandrova, V. G. Avakyan, and D. S. Zhuk, Izv. Akad. Nauk SSSR, Ser. Khim.,140 (1973).

  10. E. Plötz and E. Wernhardt, Patent No. 85846 (GFR), Chem. Abstr.,52, 10200d (1958).

    Google Scholar 

  11. R. G. Kostyanovskii and V. P. Leshchinskaya, Inventor's Certificate 1,364,620 (USSR), Byull. Izobret., No. 1 (1988).

  12. R. G. Kostyanovskii and V. F. Bystrov, Dokl. Akad. Nauk SSSR,148, 839 (1963); R. G. Kostyanovskii and O. A. Yuzhakova, Dokl. Akad. Nauk SSSR,159, 142 (1964).

    Google Scholar 

  13. R. G. Kostyanovskii, Yu. I. Él'natanov, V. P. Leshchinskaya, and I. I. Chervin, Izv. Akad. Nauk SSSR, Ser. Khim., 2637 (1986).

  14. V. G. Avakyan, G. L. Gromova, L. M. Timofeeva, and D. S. Zhuk. Izv. Akad. Nauk SSSR, Ser. Khim., 1998 (1977).

  15. G. D. Jones, J. Org. Chem.,9, 484 (1944).

    Google Scholar 

  16. I. I. Chervin, A. A. Fomichev, A. S. Moskalenko, et al., Izv. Akad. Nauk SSSR, Ser. Khim., 1110 (1988); I. I. Chervin, A. É. Aliev, V. N. Voznesenskii, et al., Izv. Akad. Nauk SSSR, Ser. Khim., 1917 (1987).

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2566–2575, November, 1988.

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Kostyanovskii, R.G., Leshchinskaya, V.P., Alekperov, R.K. et al. Oligomers of aziridines and N-β-aziridinoethylamides. Russ Chem Bull 37, 2315–2323 (1988). https://doi.org/10.1007/BF00959886

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  • DOI: https://doi.org/10.1007/BF00959886

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