Stereospecific synthesis of a key synthon for faranal — The trail pheromone of the antMonomorium pharaonis
✍ Scribed by A. N. Kasatkin; T. Yu. Romanova; I. P. Podlipchuk; G. A. Tolstikov
- Publisher
- Springer
- Year
- 1993
- Tongue
- English
- Weight
- 304 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0009-3130
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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
The poison gland of the Pharaoh's ant contains two attractive alcaloidal pheromones, which are components of its odour trail l-3 . The Dufour's gland, however, produces trace amounts of a much more active compound, the true trail pheromone. We now wish to describe
A Stereospecific Synthesis of Both Enantiomers of 2-(1'-Amino-2'methylpropyl)imidazole, a Key Synthon in the Synthesis of SB 203386; a Potent Protease Inhibitor. -Two different diastereospecific approaches to chiral 2-(1-amino-2-methylpropyl)imidazoles (VI), parts of the inhibitor (VII), are develop