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Russian Journal of General Chemistry

, Volume 88, Issue 10, pp 2204–2208 | Cite as

Mannich Bases from Bicyclo[2.2.1]hept-5-en-2-ylmethanol, Secondary Amines and Formaldehyde

  • E. H. MammadbayliEmail author
  • G. E. Hajiyeva
  • S. I. Ibrahimli
  • N. A. Jafarova
Letters to the Editor
  • 6 Downloads

Abstract

New Mannich bases were synthesized by reacting bicyclo[2.2.1]hept-5-en-2-ylmethanol with secondary amines and formaldehyde. Physicochemical characteristics, composition and structure of the synthesized compounds were determined by elemental analysis, IR, 1H, 13C NMR spectroscopy and mass spectrometry.

Keywords

dicyclopentadiene bicyclo[2.2.1]hept-5-en-2-ylmethanol secondary amines Mannich bases 

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References

  1. 1.
    Kuliev, A.M., Khimiya i tekhnologiya prisadok k maslam i toplivam (Chemistry and Technology of Oil and Fuel Additives), Moscow: Khimiya, 1972.Google Scholar
  2. 2.
    Markova, I.V., Mikhailov, I.B., and Nezhentsev, M.V., Farmakologiya (Pharmacology), St. Petersburg: Foliant, 2001.Google Scholar
  3. 3.
    Kas’yan, L.I., Kas’yan, A.O., Okovityi, S.I., and Tarabara, I.N., Aminy s karkasnymy fragmentami i ikh proizvodnye (Amines with Cage Fragments and Their Derivatives), Dnepropetrovsk: Dnepropetr. Univ., 2009.Google Scholar
  4. 4.
    Mashkovskii, M.D., Lekarstvennye sredstva (Drugs), Moscow: Novaya Volna, 2002, vol.1.Google Scholar
  5. 5.
    Goulioukina, N.S., Makukhin, N.N., and Beletskaya, I.P., Russ. Chem. Rev., 2016, vol. 85, no. 7, p. 667. doi 10.1070/rcr4579CrossRefGoogle Scholar
  6. 6.
    Tandura, S.N., Shumsky, A.N., Litvin, E.F., Kozlova, L.M., Shuvalova, E.V., Sharf, V.Z., and Kolesnikov, S.P., Russ. Chem. Bull., 2001, vol. 50, no. 6, p. 1014.CrossRefGoogle Scholar
  7. 7.
    Azizi, N. and Saidi, M.R., Org. Lett., 2005, vol. 7, no. 17, p. 3649. doi 10.1021/o1051220qCrossRefGoogle Scholar
  8. 8.
    Fernandez-Rodriguez, M.A., Shen, Q., and Hartwing, Z.F., J. Am. Chem. Soc., 2006, vol. 128, no. 7, p. 2180. doi 10.1021/ja0580340CrossRefGoogle Scholar
  9. 9.
    Zhu, D., Xu, L., Wu, F., and Wan, B., Tetrahedron Lett., 2006, vol. 47, no. 32, p. 5781. doi 10.1016/j.tetlet.2006.05.178CrossRefGoogle Scholar
  10. 10.
    Devi, N.S. and Perumal, S., Tetrahedron Lett., 2007, vol. 48, no. 32, p. 5627. doi 10.1016/j.tetlet.2007.06.024CrossRefGoogle Scholar
  11. 11.
    Dziedzic, P., Ibrahem, I., and Cordova, A., Tetrahedron Lett., 2008, vol. 49, no. 5, p. 803. doi 10.1016/j.tetlet.2007.11.196CrossRefGoogle Scholar
  12. 12.
    Gasanov, A.G., Sadykhov, F.M., and Musaev, M.R., Tsyklopentadien i ego prevrashcheniya (Cyclopentadiene and Its Transformations), Baku: Gorgud, 1998.Google Scholar
  13. 13.
    Gordon, A.J. and Ford, R.A., The Chemist’s Companion, New York: Wiley, 1972.Google Scholar

Copyright information

© Pleiades Publishing, Ltd. 2018

Authors and Affiliations

  • E. H. Mammadbayli
    • 1
  • G. E. Hajiyeva
    • 1
  • S. I. Ibrahimli
    • 2
  • N. A. Jafarova
    • 3
  1. 1.Institute of Petrochemical Processes of the National Academy of Sciences of AzerbaijanBakuAzerbaijan
  2. 2.Ganja State UniversityGanjaAzerbaijan
  3. 3.Azerbaijan State University of Oil and IndustryBakuAzerbaijan

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