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Chemistry of Heterocyclic Compounds

, Volume 27, Issue 1, pp 64–66 | Cite as

Vinylogs of 4-pyridinaldehyde

  • L. Y. Leitis
  • D. P. Yansone
  • R. A. Skolmeistere
  • Y. Y. Popelis
  • M. P. Gavars
  • M. V. Shimanskaya
  • L. K. Maslii
  • G. S. Nikol'skaya
Article
  • 35 Downloads

Abstract

Condensation of 4-pyridinaldehyde and 3-(4′-pyridyl)acrolein with acetaldehyde in the presence of morpholine acetate has given their vinylogs. These compounds have been shown to exist mainly in the trans-configurations.

Keywords

Acetate Acetaldehyde Organic Chemistry Pyridyl Acrolein 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature Cited

  1. 1.
    W. P. Hayes and C. J. Timmons,Spectrochim. Acta,24A, 323 (1968).Google Scholar
  2. 2.
    V. I. Savin, Yu. P. Kataev, and I. I. Saidashev,Izv, Akad. Nauk SSSR, Ser. Khim., No. 4, 851 (1972).Google Scholar
  3. 3.
    G. V. Kryshtal', L. A. Yanovskaya, and V. F. Kucherov,Izv. Akad. Nauk SSSR, Ser. Khim., No. 2, 441 (1973).Google Scholar
  4. 4.
    V. I. Savin, R. G. Gainullina, V. V. Zverev, and Yu. P. Kitaev,Zh. Org. Khim.,11, 1169 (1975).Google Scholar
  5. 5.
    V. I. Savin, D. D. Churkin, and Yu. P. Kitaev,Izv. Akad. Nauk SSSR, Ser. Khim., No. 6, 1264 (1976).Google Scholar
  6. 6.
    S. M. Makin, I. E. Mikerin, O. A. Shavrygina, G. A. Ermakova, and B. M. Arshava,Zh. Org. Khim.,20, 2317 (1984).Google Scholar
  7. 7.
    V. M. Nikitenko, I. K. Polyakov, and S. B. Tsukerman,Preparative Methods for Chemical Reagents [in Russian], All-Union Institute for Chemical Reagents and Specially Pure Chemical Compounds, Moscow (1970), No. 22, p. 142.Google Scholar
  8. 8.
    L. M. Jackman and S. Sternhell,Applications of NMR Spectroscopy in Organic Chemistry, Pergamon Press, New York (1969), p. 122.Google Scholar
  9. 9.
    V. I. Savin, I. D. Temyachev, and Yu. P. Kitaev,Zh. Org. Khim.,10, No. 8, 1590 (1974).Google Scholar
  10. 10.
    L. S. Davies,J. Chem. Soc.,36, 2284 (1971).Google Scholar
  11. 11.
    L. Shi, W. Xia, J. Yang, X. Wen, and Y. Z. Huang,Tetrahedron Lett.,28, 2155 (1987).Google Scholar
  12. 12.
    EPA/NIH Mass Spectral Data Base, US Government Printing Office, Washington (1978), Vol. 1.Google Scholar
  13. 13.
    L. Ya. Leitis, K. I. Rubina, Yu. S. Gol'dberg, D. P. Yansone, and M. V. Shimanskaya,Izv. Akad. Nauk Latv. SSR, Ser. Khim., No. 4, 459 (1980).Google Scholar
  14. 14.
    L. Ya. Leitis and M. V. Shimanskaya,Khim. Geterotsikl. Soedin., No. 3, 507 (1967).Google Scholar

Copyright information

© Plenum Publishing Corporation 1991

Authors and Affiliations

  • L. Y. Leitis
    • 1
  • D. P. Yansone
    • 1
  • R. A. Skolmeistere
    • 1
  • Y. Y. Popelis
    • 1
  • M. P. Gavars
    • 1
  • M. V. Shimanskaya
    • 1
  • L. K. Maslii
    • 1
  • G. S. Nikol'skaya
    • 1
  1. 1.Institute of Organic SynthesisAcademy of Sciences of the Latvian SSRRiga

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