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ChemInform Abstract: Pheromone Synthesis. Part 191. Synthesis of the Enantiomers of 8-Hydroxy-2,5,8-trimethyl-4-nonanone, the Myxobacterial Pheromone of Stigmatella aurantiaca to Induce the Formation of Its Fruiting Body.

โœ Scribed by K. MORI; M. TAKENAKA

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

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Synthesis of the Enantiomers of 8-Hydrox
Synthesis of the Enantiomers of 8-Hydroxy-2,5,8-trimethyl-4-nonanone, the Myxobacterial Pheromone of Stigmatella aurantiaca to Induce the Formation of Its Fruiting Body
โœ Kenji Mori; Motonobu Takenaka ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 121 KB ๐Ÿ‘ 1 views

The enantiomers of the title compound 1 were synthesized bacterium Stigmatella aurantiaca at a concentration of 0.4ฯช1.0 nM. from the enantiomers of citronellol (2). Both (R)-and (S)-1 induced the formation of the fruiting body of a myxo-

ChemInform Abstract: Pheromone Synthesis
ChemInform Abstract: Pheromone Synthesis. Part 193. Simple Synthesis of (.+-.)-Stigmolone (8-Hydroxy-2,5,8-trimethyl-4-nonanone), the Pheromone of Stigmatella aurantiaca.
โœ Kenji Domon; Kenji Mori ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 31 KB

Pheromone Synthesis. Part 193. Simple Synthesis of (ยฑ)-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.