Both the enantiomers of 9-methylgermacrene-B (1) were synthesized from the enantiomers of methyl 3-hydroxy-2methylpropanoate (2). The male-produced sex pheromone of
Analysis of the sex pheromone extract of individual male Lutzomyia longipalpis sandflies from six regions in Brazil
โ Scribed by J.G.C. Hamilton; R.D.C. Maingon; B. Alexander; R.D. Ward; R.P. Brazil
- Book ID
- 108886940
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 270 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0269-283X
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Four stereoisomers (1a-d) of (ยฑ)-3-methyl-ฮฑ-himachalene produced sex pheromone of the sandfly Lutzomyia longipalpis was shown to possess the structure and relative were synthesized by employing the intramolecular Diels-Alder reaction of (ยฑ)-14 to (ยฑ)-18 as the key-step. The male-configuration as dep
1S,3S,7R)-3-Methyl-a-himachalene, the sex pheromone of the male sandยฏy (Lutzomyia longipalpis) from Jacobina, Brazil, was synthesized enantioselectively by employing Evans' or Oppolzer's asymmetric methylation as the key step. The absolute conยฎguration at the ring junction of this pheromone is oppos
## Both germacrene-B (2) and 9-methylgermacrene-B [(ยฑ)-1] shown to be the racemate of the male-produced sex pheromone of the sandfly Lutzomyia longipalpis from were synthesized by employing cyclization reactions [8 ว 9 and (ยฑ)-20 ว (ยฑ)-21] as the key steps. The latter [(ยฑ)-1] was Lapinha, Brazil.