Synthesis and antifeeding activities of Tonghaosu analogues

J Agric Food Chem. 2004 Nov 3;52(22):6719-23. doi: 10.1021/jf049479v.

Abstract

Tonghaosu (1), a lead for a botanical antifeedant, and its 22 analogues were synthesized according to a previously reported concise and straightforward procedure. The structures of all new compounds were confirmed by NMR, IR, MS, and HREIMS or elemental analysis. Their insect antifeedant activities against the large white butterfly (Pieris brassicae L.) were examined, and six analogues (Z- and E-6h and Z-isomers of 6i-l), which contain 1,3-diyn or 3,4-methylenedioxyphenyl acetylene group, showed considerable antifeedant activity. Interestingly, Z-isomers of 6i-k are much more active than their corresponding E-isomers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / analysis*
  • Alkynes / chemistry
  • Alkynes / pharmacology
  • Animals
  • Butterflies / physiology*
  • Chrysanthemum / chemistry
  • Eating / drug effects*
  • Insecticides / chemical synthesis*
  • Spiro Compounds / analysis*
  • Spiro Compounds / chemistry
  • Spiro Compounds / pharmacology

Substances

  • Alkynes
  • Insecticides
  • Spiro Compounds
  • tonghaosu