✦ LIBER ✦

ChemInform Abstract: First Asymmetric Synthesis of Stigmolone: The Fruiting Body Inducing Pheromone of the Myxobacterium Stigmatella aurantiaca.

✍ Scribed by Dieter Enders; Andre Ridder

Publisher: John Wiley and Sons
Year: 2001
Weight: 30 KB
Volume: 32
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200108226

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Two-Step Synthesis

ChemInform Abstract: Two-Step Synthesis of (.+-.)-Stigmolone, the Pheromone of Stigmatella aurantiaca.

✍ Oleg L. Epstein; Oleg G. Kulinkovich 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB

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.

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

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.

ChemInform Abstract: Pheromone Synthesis

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.

✍ K. MORI; M. TAKENAKA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

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

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

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-

ChemInform Abstract: Asymmetric Total Sy

ChemInform Abstract: Asymmetric Total Synthesis of the Caribbean Fruit Fly Pheromone (+)- Epianastrephin.

✍ A. G. SCHULTZ; S. J. KIRINCICH 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Asymmetric Total Synthesis of the Caribbean Fruit Fly Pheromone (+)-Epianastrephin. -The chiral title compound (XI) is synthesized from the chiral benzamide (I) in 15 steps and 9.5% overall yield and ¿ 98% enantiomeric excess. -(SCHULTZ, A.