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Simple Synthesis of (±)-Stigmolone (8-Hydroxy-2,5,8-trimethyl-4-nonanone), the Pheromone of Stigmatella aurantiaca

✍ Scribed by Kenji Domon; Kenji Mori

Publisher: John Wiley and Sons
Year: 1999
Tongue: English
Weight: 205 KB
Volume: 1999
Category: Article
ISSN: 1434-193X
DOI: 10.1002/(sici)1099-0690(199905)1999:5<979::aid-ejoc979>3.0.co;2-c

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ChemInform Abstract: Pheromone Synthesis

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✍ Kenji Domon; Kenji Mori 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Pheromone Synthesis. Part 193. Simple Synthesis of (±)-Stigmolone (8-Hydroxy-2,5,8-trimethyl-4-nonanone), the Pheromone of Stigmatella aurantiaca. -Stigmolone (VIII), which induces the formation of the fruiting body of S. aurantiaca, is synthesized from ketone (I) in 48% overall yield in four steps.

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✍ Kenji Mori; Motonobu Takenaka 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 121 KB 👁 1 views

The enantiomers of the title compound 1 were synthesized bacterium Stigmatella aurantiaca at a concentration of 0.4Ϫ1.0 nM. from the enantiomers of citronellol (2). Both (R)-and (S)-1 induced the formation of the fruiting body of a myxo-

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v