✦ LIBER ✦

Efficient asymmetric synthesis of long chain methyl-branched hydrocarbons, components of the contact sex pheromone of females of the cerambycid beetle, Neoclytus acuminatus acuminatus

✍ Scribed by Bello, Jan E.; Millar, Jocelyn G.

Book ID: 120545566
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 461 KB
Volume: 24
Category: Article
ISSN: 0957-4166
DOI: 10.1016/j.tetasy.2013.05.021

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of the Enantiomers of (Z)-21-M

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 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB 👁 1 views

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 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

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)-