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 language | English |
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Pages (from-to) | 761–766 |
Journal | Beilstein Journal of Organic Chemistry |
Volume | 10 |
Publication status | Published - 2 Apr 2014 |
Externally published | Yes |
Keywords
- organic chemistry
- total synthesis
- natural product
- asymmetric catalysis