Asymmetric total synthesis of a putative sex pheromone component from the parasitoid wasp Trichogramma turkestanica

Danny Geerdink, Jeffrey Buter, Teris van Beek, Adriaan Minnaard

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Virgin females of the parasitoid wasp Trichogramma turkestanica produce minute amounts of a sex pheromone, the identity of which has not been fully established. The enantioselective synthesis of a putative component of this pheromone, (6S,8S,10S)-4,6,8,10-tetramethyltrideca-2E,4E-dien-1-ol (2), is reported as a contribution to this identification. Catalytic asymmetric conjugate addition of methylmagnesium bromide and stereoselective Horner–Wadsworth–Emmons olefinations are used as the key steps, and 2 was obtained in 16 steps with an overall yield of 4.4%.
Original languageEnglish
Pages (from-to)761–766
JournalBeilstein Journal of Organic Chemistry
Volume10
Publication statusPublished - 2 Apr 2014
Externally publishedYes

Keywords

  • organic chemistry
  • total synthesis
  • natural product
  • asymmetric catalysis

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