Enantioselective synthesis and determination of the absolute configuration of the male sex pheromone of the parasitoid wasp Urolepis rufipes
Author:
Affiliation:
1. Technische Universität Braunschweig
2. Institute of Organic Chemistry
3. 38106 Braunschweig
4. Germany
5. Universität Regensburg
6. Institute of Zoology
7. 93053 Regensburg
Abstract
The parasitoid wasp Urolepis rufipes uses terminally oxidized dihydrolinalool as a sex pheromone. The absolute configuration of the active enantiomer was established as 2S,6S by synthesis and its pheromonal activity was proven in a bioassay.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00614A
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