3,7,7-trimethyl-1,3,5-cycloheptatriene in volatiles of female mountain pine beetles,Dendroctonus ponderosae
✍ Scribed by G. Gries; J. H. Borden; H. D. Pierce; B. D. Johnston; A. C. Oehlschlager
- Book ID
- 105084941
- Publisher
- Springer
- Year
- 1992
- Tongue
- English
- Weight
- 176 KB
- Volume
- 79
- Category
- Article
- ISSN
- 0028-1042
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Both (1__R__)‐ and (1__S__)‐hydroxy derivatives of (+)‐exo‐brevicomin {(1__R__,1′__R__,5′__R__,7′__R__)‐1‐(5′‐methyl‐6′,8′‐dioxabicyclo[3.2.1]‐octyl)ethanol (1) and its (1__S__)‐isomer (2)} were synthesized by employing Sharpless asymmetric dihydroxylation as the key reaction.
## Abstract Both (2__R__)‐ and (2__S__)‐hydroxy derivatives of (+)‐exo‐brevicomin {5‐methyl‐6,8‐dioxabicyclo[3.2.1]octan‐2‐ol; 1 and 2} were synthesized by employing Sharpless asymmetric dihydroxylation as the key reaction.
Pheromone Synthesis. Part 183. Synthesis of (1R,2R,5S,7R)-and (1R,2S, 5S,7R)-2-Hydroxy-exo-brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae. -Both title compounds (V) and (VI) are synthesized via asymmetric dihydroxylation as the key ste