Skip to main content

Synthesis, Structure Activity Relationships and Mode of Action of Insect Pheromones

A Contribution for the Transmission of Chemical Information in Nature

  • Conference paper
Book cover Natural Product Chemistry

Abstract

Insect pheromones are signal substances which effect the transmission of chemical information between the individua of an insect species. Female butterflies and moths in many cases use mono- and bisolefinic aldehydes, alcohols and acetates1) as their species specific sex pheromones. The corresponding male moths possess specialized sensory cells in their antennae, the dendrites of which end in the sensory hairs (sensilla). The odor molecules impinge on the antennal cuticle and reach the dendritic membrane by diffusion via pores and tubuli, where they interact with specific acception sites.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. H.J. Bestmann and O. Vostrowsky, in SPI Chemie der Pflanzenschutz-Schädlingsbekämpfungsmittel (R. Wegler, ed.), Vol. 6 p. 29, Springer Verlag Berlin-Heidelberg (1980).

    Google Scholar 

  2. D. Schneider, Z vergl. Physiol. 40, 9 (1957).

    Article  Google Scholar 

  3. H.J. Bestmann, O. Vostrowsky and W. Stransky, Chem Ber. 109, 1964.

    Google Scholar 

  4. H.J. Bestmann, O. Vostrowsky, W. Stransky and P. Range, Chem. Ber. 108, 3582 (1975).

    Article  CAS  Google Scholar 

  5. H.J. Bestmann, I. Kantardjiew, P. Rösel, W. Stransky and O. Vostrowsky, Chem Ber. 111, 248 (1978).

    Article  CAS  Google Scholar 

  6. H.J. Bestmann, K.H. Koschatzky and O. Vostrowsky, Chem Ber. 112, 1923 (1979).

    Article  CAS  Google Scholar 

  7. H.J. Bestmann and A. Bomhard, unpublished.

    Google Scholar 

  8. H.J. Bestmann and A. Bomhard, Angew Chem 94, 562 (1982);

    Article  CAS  Google Scholar 

  9. H.J. Bestmann and A. Bomhard, Intern. Ed. Engl 21, 545 (1982).

    Article  Google Scholar 

  10. H.J. Bestmann and B. Arnason, Chem Ber. 95, 1513 (1962).

    Article  CAS  Google Scholar 

  11. H.J. Bestmann, K. Kumar and L. Kisielowski, Chem. Ber. 116, 2378 (1983).

    Article  CAS  Google Scholar 

  12. H.J. Bestmann and K. Kumar, Angew Chem. 95, 154 (1983).

    Article  CAS  Google Scholar 

  13. H.J. Bestmann and K. Li, Chem Ber. 115, 828 (1982).

    Article  CAS  Google Scholar 

  14. F. Ramirez, N.B. Desai and N. McKelvie, J Amer Chem Soc. 84, 1745 (1962).

    Article  CAS  Google Scholar 

  15. E.J. Corey and P.L. Fuchs, Tetrahedron Lett. 1972, 3769

    Google Scholar 

  16. H.J. Bestmann and H. Frey, Liebigs Ann Chem 1980, 2061.

    Google Scholar 

  17. H.C. Brown, J.A. Sinclair and M.M. Midland, J. Amer Chem Soc. 95, 3080 (1973).

    Article  Google Scholar 

  18. H.J. Bestmann, K. Sühs and T. Röder, Angew Chem. 93, 1098 (1981);.

    Article  CAS  Google Scholar 

  19. H.J. Bestmann, K. Sühs and T. Röder, Int. Ed. Engl 20, 1038 (1981).

    Article  Google Scholar 

  20. H.J. Bestmann and T. Röder, Angew Chem 95, 812 (1983);

    Article  CAS  Google Scholar 

  21. H.J. Bestmann and T. Röder, Intern. Ed. Engl 22, 782 (1983).

    Article  Google Scholar 

  22. H.J. Bestmann, Pure Appl. Chem. 51, 515 (1979);

    Article  CAS  Google Scholar 

  23. H.J. Bestmann, Pure Appl. Chem. 52, 77 (1980).

    Article  Google Scholar 

  24. H.J. Bestmann and O. Vostrowsky, SPI in Topics in Current Chemistry 109, 85 (1983).

    Google Scholar 

  25. H.J. Bestmann, J. Süss and O. Vostrowsky, Liebigs Ann Chem 1981,2117.

    Google Scholar 

  26. H.J. Bestraann, K. Roth and M. Ettlinger, Chem Ber. 115, 161 (1982)

    Article  Google Scholar 

  27. H.J. Bestmann and P. Erman, Chem Ber. 116, 3269 (1983).

    Google Scholar 

  28. H.J. Bestmann and J. Süss, Liebigs Ann Chem 1982, 363.

    Google Scholar 

  29. H.J. Bestmann, A. Bomhard, R. Dötzer and O. Vostrowsky, unpublished.

    Google Scholar 

  30. H.J. Bestmann, K.H. Koschatzky, A. Plenchette, J. Süss and O. Vostrowsky, Liebigs Ann Chem 1982, 536.

    Google Scholar 

  31. H.J. Bestmann and K. Li, Tetrahedron Lett 1981, 4941.

    Google Scholar 

  32. H.J. Bestmann, P. Rösel and O. Vostrowsky, Liebigs Ann Chem 1979, 1189.

    Google Scholar 

  33. O. Vostrowsky, H.J. Bestmann and E. Priesner, Nachr Chem Techn 21, 501 (1973).

    Article  Google Scholar 

  34. E. Priesner, M. Jacobson and H.J. Bestmann, Z Naturforsch. 30C, 283 (1975).

    CAS  Google Scholar 

  35. E. Priesner, H.J. Bestmann, P. Rösel and O. Vostrowsky, Z. Naturforsch. 32c, 979 (1977).

    CAS  Google Scholar 

  36. H.J. Bestmann, K.H. Koschatzky, O. Vostrowsky and E. Priesner, in preparation.

    Google Scholar 

  37. O.L. Chapman, K.C. Mattes, R.S. Sheridan, and J.A. Klun, J. Amer Chem Soc. 100, 4878 (1978).

    Article  CAS  Google Scholar 

  38. H.J. Bestmann, H.L. Hirsch, H. Platz, M. Rheinwald and O. Vostrowsky, Angew Chem 92, 492; (1980).

    Article  CAS  Google Scholar 

  39. H.J. Bestmann, H.L. Hirsch, H. Platz, M. Rheinwald and O. Vostrowsky, Int Ed Engl 19, 475 (1980).

    Article  Google Scholar 

  40. E. Sackmann, in Biophysik (W. Hoppe, W. Lohmann, H. Markl and H. Ziegler, eds.), Springer Verlag, Berlin Heidelberg, New York, p. 316 (1978).

    Google Scholar 

  41. H. Träuble, Naturwissenschaften 58, 277 (1971).

    Article  PubMed  Google Scholar 

  42. R. Wax, Diplomarbeit University Erlangen-Nürnberg (1979).

    Google Scholar 

  43. E. Neumann, Angew Chem. 85, 430 (1973).

    Article  CAS  Google Scholar 

  44. H.J. Bestmann and K. Dippold, Naturwissenschaften 70, 47 (1983).

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1986 Springer-Verlag Berlin Heidelberg

About this paper

Cite this paper

Bestmann, H.J. (1986). Synthesis, Structure Activity Relationships and Mode of Action of Insect Pheromones. In: Rahman, Au. (eds) Natural Product Chemistry. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71425-2_3

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-71425-2_3

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-71427-6

  • Online ISBN: 978-3-642-71425-2

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics