Chemistry of Natural Compounds

, Volume 5, Issue 4, pp 231–236 | Cite as

Mass and NMR spectra of haplophyllidine and perforine and of their derivatives

  • I. A. Bessonova
  • Z. Sh. Faizutdinova
  • Ya. V. Rashkes
  • M. R. Yagudaev
  • S. Yu. Yunusov
Article
  • 15 Downloads

Conclusions

The mass and NMR spectra of haplophyllidine, perforine, and their derivatives have been studied. The influence of the open and cyclic forms of the molecular ion on the nature of the fragmentation has been discussed. The main routes of fragmentation of the compounds considered are due to the presence of substituents at C8 and C4.

Keywords

Methoxyl Group Olefinic Proton Cyclic Form Isopropylidene Tetrahydroquinoline 

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References

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    Z. Sh. Faizutdinova, I. A. Bessonova, and S. Yu. Yunusov, KhPS [Chemistry of Natural Compounds],3, 356, 1967; vol. 4, 360, 1968.Google Scholar
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    G. Budzikiewicz, C. Djerassi, and D. Williams, Interpretation of Mass Spectra of Organic Compounds [Russian translation], Moscow, 1966; J. Beynon, Mass Spectrometry and Its Applications to Organic Chemistry [Russian translation], Moscow, 1964; Canad. J. Chem.,43, 5216, 1965.Google Scholar
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Copyright information

© Consultants Bureau 1972

Authors and Affiliations

  • I. A. Bessonova
    • 1
  • Z. Sh. Faizutdinova
    • 1
  • Ya. V. Rashkes
    • 1
  • M. R. Yagudaev
    • 1
  • S. Yu. Yunusov
    • 1
  1. 1.Institute of the Chemistry of Plant Substances AS UzSSRUSSR

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