ChemInform Abstract: Enantioselective Synthesis of (S)-(+)-2-Tridecanol Acetate, an Aggregation Pheromone Component of Drosophila mulleri.

ChemInform ◽  
2010 ◽  
Vol 23 (4) ◽  
pp. no-no
Author(s):  
D. ENDERS ◽  
A. PLANT
2004 ◽  
Vol 136 (3) ◽  
pp. 419-425 ◽  
Author(s):  
N.L. Jeans Williams ◽  
J.H. Borden

AbstractIn past field studies, the greatest response of western balsam bark beetles, Dryocoetes confusus Swaine, to traps was obtained with blends of (+)-exo-brevicomin and (+)- or (±)-endo-brevicomin, which imitate the natural male-produced aggregation pheromone. We conducted a trapping experiment comparing low-release enanti ospecific blends (9:1 (+)-exo-brevicomin:(+)-endo-brevicomin or 9:2 (+)-exo-brevicomin:(±)-endo-brevicomin released at 0.3, 0.1, or 0.03 mg per day) with the standard commercial (±)-exo-brevicomin bait released at 1.2 mg per day. Multiple-funnel traps baited with the experimental blends caught more D. confusus than the unbaited traps, but only traps with the 9:2 (+):(±) blend released at 0.3 and 0.03 mg per day caught significantly more male and female beetles than those baited with the standard bait. Thus, trap sensitivity can be improved with the addition of (±)-endo-brevicomin. The sympatric bark beetle D. autographus Ratzeburg was captured in significant numbers in traps baited with (±)-exo-brevicomin. A subsequent trapping experiment showed that D. autographus responded to (+)- or (±)-exo-brevicomin, but not to (−)-exo-brevicomin, suggesting that (+)-exo-brevicomin is the principal aggregation pheromone component in this species.


2018 ◽  
Vol 67 (1) ◽  
pp. 72-80 ◽  
Author(s):  
Angel Guerrero ◽  
Victoria Elena Ramos ◽  
Sergio López ◽  
José María Alvarez ◽  
Aroa Domínguez ◽  
...  

1983 ◽  
Vol 14 (18) ◽  
Author(s):  
A. LAGRANGE ◽  
A. OLESKER ◽  
S. S. COSTA ◽  
G. LUKACS ◽  
T. T. THANG

2014 ◽  
Vol 10 ◽  
pp. 761-766 ◽  
Author(s):  
Danny Geerdink ◽  
Jeffrey Buter ◽  
Teris A van Beek ◽  
Adriaan J Minnaard

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%.


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