960化工网
Enantioselective synthesis and determination of the absolute configuration of the male sex pheromone of the parasitoid wasp Urolepis rufipes†
Kristina Melnik,Christopher Grimm,Johannes Wittbrodt,Joachim Ruther,Stefan Schulz
Organic & Biomolecular Chemistry Pub Date : 04/08/2020 00:00:00 , DOI:10.1039/D0OB00614A
Abstract

Males of the parasitoid wasp Urolepis rufipes use 2,6-dimethyl-7-octene-1,6-diol as a sex pheromone to attract virgin females. Herein, we determine the absolute configuration of the pheromone to be (2S,6S)-2,6-dimethyl-7-octene-1,6-diol (2S,6S-6) and present a stereoselective synthesis of the natural enantiomer of this new linalool derivative. In addition, we show that female wasps respond to the natural 2S,6S-6 stereoisomer while 2R,6S-6 is behaviorally inactive.

Graphical abstract: Enantioselective synthesis and determination of the absolute configuration of the male sex pheromone of the parasitoid wasp Urolepis rufipes
平台客服
平台客服
平台在线客服