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ChemInform Abstract: Syntheses of Cyclobutane Derivatives: Total Synthesis of (+) and (-) Enantiomers of the Oleander Scale Aspidiotus nerii Sex Pheromone.

✍ Scribed by Francois-Didier Boyer; Paul-Henri Ducrot

Publisher
John Wiley and Sons
Year
2010
Weight
38 KB
Volume
30
Category
Article
ISSN
0931-7597

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Syntheses of Cyclobutane Derivatives: To
Syntheses of Cyclobutane Derivatives: Total Synthesis of (+) and (–) Enantiomers of the Oleander Scale Aspidiotus nerii Sex Pheromone
✍ FranΓ§ois-Didier Boyer; Paul-Henri Ducrot πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 374 KB πŸ‘ 1 views

Synthesis of both enantiomers of the Aspidiotus nerii sex asymmetric centers. Stereoselective synthesis of a number of other trisubstituted cyclobutane derivatives also proves the pheromone and their diastereomers has been achieved using, as a key step, an intramolecular ester enolate versatility of

ChemInform Abstract: Pheromone Synthesis
ChemInform Abstract: Pheromone Synthesis. Part 194. Synthesis of the Enantiomers of (Z)-21-Methyl-8-pentatriacontene, the Major Component of the Female-Produced Contact Sex Pheromone of the Yellow-Spotted Longicorn Beetle, Psacothea hilaris.
✍ Kenji Domon; Hirosato Takikawa; Kenji Mori πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 28 KB

Pheromone Synthesis. Part 194. Synthesis of the Enantiomers of (Z)-21-Methyl-8-pentatriacontene, the Major Component of the Female-Produced Contact Sex Pheromone of the Yellow-Spotted Longicorn Beetle, Psacothea hilaris. -The (R)-enantiomer of the title compound (I) is synthesized starting from (S)-