Absolute configuration of (3R,4S)-4-methyl-3-hexanol—A pheromone from the head of the ant Tetramorium impurum foerster
✍ Scribed by J.M. Pasteels; J.C. Verhaeghe; R. Ottinger; J.C. Braekman; D. Daloze
- Book ID
- 113167918
- Publisher
- Elsevier Science
- Year
- 1981
- Weight
- 303 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0020-1790
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The relative configuration of the naturally occurring 3‐methyl‐4‐octanol (1), the male‐produced aggregation pheromone of __Rhynchophorus phoenicis__, was determined as __syn__ by a GC comparison of the synthetic (±)‐__syn__‐ and (±)‐__anti__‐1 with the natural product. Enantioselective
## Abstract Faranal (1), the trail‐following pheromone of the worker of Pharaoh's ant (__Monomorium pharaonis__), was synthesized by the coupling reaction of the iododiene 3 with the chiral building block 8 as the key step. The geometrically pure iododiene 3 was prepared by the zirconocene‐mediated