Advertisement

Chemistry of Natural Compounds

, Volume 46, Issue 6, pp 886–891 | Cite as

Humulene and its derivatives from Betula pendula buds

  • D. N. Vedernikov
  • V. I. Roshchin
Article

Humulene and its derivatives (6R)-hydroxy-α-humulene [(6R)-hydroxy-(1E,4E,8E)-4,8,11,11tetramethylcycloundeca-1,4,8-triene], (6R)-acetoxy-α-humulene [(6R)-acetoxy-(1E,4E,8E)-4,8,11,11tetramethylcycloundeca-1,4,8-triene], a coumaric acid ester, 14-hydroxy-α-humulene [14-coumaroxy(1E,4E,8E)-4,8,11,11-tetramethylcycloundeca-1,4,8-triene], (1E,6R,8E)-4,5-epoxy-6-hydroxy-4,8,11,11tetramethylcycloundeca-1,8-diene, and (6R,9S)-4,11,11-trimethyl-8-methylene-1,4-cycloundecadien-6,9-diol were observed in the hydrocarbon extract of Betula pendula (Betulaceae) buds. The GC retention indices were determined for all identified compounds.

Keywords

humulene humulene derivatives vegetative buds hydrocarbon extract Betula pendula 

References

  1. 1.
    D. N. Vedernikov and V. I. Roshchin, Khim. Rastit. Syr’ya, No. 3, 69 (2009).Google Scholar
  2. 2.
    D. N. Vedernikov and V. I. Roshchin, Khim. Rastit. Syr’ya, No. 3, 75 (2009).Google Scholar
  3. 3.
    D. N. Vedernikov, N. G. Galashkina, and V. I. Roshchin, Rastit. Resur., 3, 84 (2007).Google Scholar
  4. 4.
    A. F. Barrero and J. E. Oltra, Flavour Fragrance J., 8, 185 (1993).CrossRefGoogle Scholar
  5. 5.
    N. P. Damodaran and S. Dev, Tetrahedron, 24, 4133 (1968).CrossRefGoogle Scholar
  6. 6.
    A. F. Barrero, M. M. Herrador, and P. Arteaga, Phytochemistry, 31, 203 (1992).CrossRefGoogle Scholar
  7. 7.
    R. Randriamiharisoa, E. M. Gaydou, R. Faure, and J. P. Bianchi, Magn. Reson. Chem., 24, 275 (1986).CrossRefGoogle Scholar
  8. 8.
    A. F. Barrero, M. M. Herrador, and P. Arteaga, Phytochemistry, 31, 203 (1992).CrossRefGoogle Scholar
  9. 9.
    F. Bohlmann, W. F. Abraham, and W. S. Sheldrick, Phytochemistry, 19, 869 (1980).CrossRefGoogle Scholar
  10. 10.
    W.-Y. Tsui and G. D. Brown, J. Nat. Prod., 59, 1084 (1996).CrossRefGoogle Scholar
  11. 11.
    S. Takeda, Y. Iimura, K. Tanaka, E. Kurosawa, and T. Suzuki, Chem. Lett., 155 (1990).Google Scholar
  12. 12.
    V. I. Roshchin, R. A. Baranova, O. A. Belozerskikh, and V. A. Solov’ev, Khim. Drev., No. 4, 56 (1983).Google Scholar

Copyright information

© Springer Science+Business Media, Inc. 2011

Authors and Affiliations

  1. 1.S. M. Kirov St. Petersburg State Forestry AcademySt. PetersburgRussia

Personalised recommendations