Design, synthesis, and insecticidal activities of novel monohalovinylated pyrethroids

J Agric Food Chem. 2011 Feb 23;59(4):1171-7. doi: 10.1021/jf103908d. Epub 2011 Jan 28.

Abstract

A series of novel monohalovinylated pyrethroids are designed and synthesized to replace one halo atom with a hydrogen atom on the double bond of dihalopyrethroids. Bioassays indicate that some of the synthesized compounds, such as 3j and 1j, exhibit high insecticidal activities against mosquitoes ( Culex pipiens pallens ), oriental armyworms ( Mythimna separata ), alfalfa aphids ( Aphis medicagini ), and carmine spider mites ( Tetranychus cinnabarinus ). Photolytic results of E-cis-1j suggest that monohalovinylated pyrethroids are photodegraded more easily than compound 12.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aphids
  • Culex
  • Drug Design
  • Insecticides / chemical synthesis*
  • Moths
  • Photolysis
  • Pyrethrins / chemical synthesis*
  • Pyrethrins / chemistry
  • Structure-Activity Relationship
  • Tetranychidae

Substances

  • Insecticides
  • Pyrethrins