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Synthesis and spectral properties of shielded 1,2-disubstituted imidazolines

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

Abstract

Shielded 1,2-disubstituted imidazolines were synthesized by condensation of diethylenetriamine with 2-ethylhexanoic acid. UV, IR and1H and13C NMR spectral data were discussed. The effect was studied of α branching in an alkyl substituent at the 2 position of the imidazoline ring on the spectral parameters of the synthesized compounds.

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Authors and Affiliations

  1. Institute of Chemistry, Bashkir Scientific Center, Ural Branch of the Academy of Sciences of the USSR, Ufa

    S. O. Bondareva, V. V. Lisitskii, Yu. I. Murinov, L. M. Khalilov & E. V. Vasil'eva

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  1. S. O. Bondareva
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  2. V. V. Lisitskii
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  3. Yu. I. Murinov
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  4. L. M. Khalilov
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  5. E. V. Vasil'eva
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 878–882, April, 1991.

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Bondareva, S.O., Lisitskii, V.V., Murinov, Y.I. et al. Synthesis and spectral properties of shielded 1,2-disubstituted imidazolines. Russ Chem Bull 40, 776–779 (1991). https://doi.org/10.1007/BF00958572

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  • DOI: https://doi.org/10.1007/BF00958572

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