Synthesis of mono- and disubstituted Δ<sup>2</sup>-imidazolines containing fragments of sterically hindered phenol

Authors

  • B. И. Келарев I. M. Gubkin State Oil and Gas Academy, Moscow 117917
  • B. Н. Кошелев I. M. Gubkin State Oil and Gas Academy, Moscow 117917
  • P. А. Караханов I. M. Gubkin State Oil and Gas Academy, Moscow 117917
  • B. Г. Карцев Syntest Ltd., Chernogolovka 142432
  • С. Ю. Заседателев Syntest Ltd., Chernogolovka 142432
  • А. M. Kуатбеков Syntest Ltd., Chernogolovka 142432
  • Г. B. Морозова I. M. Gubkin State Oil and Gas Academy, Moscow 117917

Abstract

Condensation of hydrochlorides of immoesters of acids of the sterically hindered phenol series with ethylenediamine and N-monosubstituted ethylenediamines was used to synthesize 2-substituted and 1,2-disubstituted Δ2-imidazolines containing fragments of 2,6-di(tert-butyl)phenol.

How to Cite
Kelarev, V. I.; Koshelev, V. N.; Karakhanov, R. A.; Kartsev, V. G.; Zasedatelev, S. Yu.; Kuatbekov, A. M.; Morozova, G. V. Chem. Heterocycl. Compd. 1995, 31, 449. [Khim. Geterotsikl. Soedin. 1995, 514.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01177016

Published

1995-04-25

Issue

Section

Original Papers