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
ChemInform Abstract: Pheromone Synthesis. Part 200. Synthesis of (S)-9-Methylgermacrene-B, the Male-Produced Sex Pheromone of the Sandfly Lutzomyia longipalpis from Lapinha, Brazil, and Its (R)-Isomer.
โ Scribed by Satoshi Kurosawa; Kenji Mori
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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๐ SIMILAR VOLUMES
## 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.
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