Advertisement

Chemistry of Natural Compounds

, Volume 6, Issue 6, pp 693–695 | Cite as

Structure of the product of the sensitized photodimerization of peucedanin

  • G. K. Nikonov
Article
  • 30 Downloads

Summary

On the basis of the NMR spectrum, a most probable structure has been proposed for the product of the sensitized photodimerization of the natural furocoumarin peucedanin. It has been shown that the latter is formed at the expense of the double bonds of the α-pyrone ring of one and of the furan ring of the second molecule in the “head to tail” manner.

Keywords

Coumarin Viti Ligo Furan Ring Lactone Ring Pyrone 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    F. Wesseli and F. Kallab, Monatsh.,59, 161, 1932.Google Scholar
  2. 2.
    F. Wesseli and K. Dirjaski, Monatsh.,64, 131, 1934.CrossRefGoogle Scholar
  3. 3.
    F. Wesseli and I. Plaichinger, Ber., 971, 75, 1942.Google Scholar
  4. 4.
    F. Wesseli and I. Kotlan, Monatsh.,86, 430 (1955).CrossRefGoogle Scholar
  5. 5.
    W. L. Fowlks, J. Invest. Dermatol.,32, No. 2, 2, 249, 1959.Google Scholar
  6. 6.
    G. Rodighiero and V. Cappellina, Gass. Chim. Ital.,91, No. 1, 103, 1961.Google Scholar
  7. 7.
    G. K. Nikonov, ZhOKh,34, 2815, 1964.Google Scholar
  8. 8.
    M. E. Perel'son, Yu. N. Shenker, G. P. Syrova, G. K. Nikonov, and A. P. Prokopenko, “The use of NMR spectroscopy in the chemistry of natural coumarins,” in: Medicinal Plants [in Russian], Vol. 15, Moscow, 1969, p. 60.Google Scholar
  9. 9.
    G. O. Schenk, I. Wilucki, and C. H. Krauch. Ber.,95, 1409, 1962.Google Scholar
  10. 10.
    G. S. Hammond, Ch. A. Stout, and A. A. Lamola, J. Am. Chem. Soc.,86, No. 15, 3103, 1964.CrossRefGoogle Scholar

Copyright information

© Consultants Bureau, a division of Plenum Publishing Corporation 1973

Authors and Affiliations

  • G. K. Nikonov

There are no affiliations available

Personalised recommendations