## Abstract For Abstract see ChemInform Abstract in Full Text.
Pheromone synthesis, CXXV. Synthesis of the four possible stereoisomers of 3,7-dimethylnonadecane, the female sex pheromone of Agromyza frontella Rondani
✍ Scribed by Mori, Kenji ;Wu, Jiang
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 473 KB
- Volume
- 1991
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
The synthesis of the four possible stereoisomers of 3,7‐dimethylnonadecane (1) has been achieved by starting from the enantiomers of methyl 3‐hydroxy‐2‐methylpropanoate (2) and (R)‐(+)‐citronellic acid (3).
📜 SIMILAR VOLUMES
The synthesis or thc Tour stereoisomers or 6,12-dimethyl-2-penladecanone (I), the sex pheromone of the banded cucumber beetle IDicihrorico hulfaato LeConte), was achieved employing the rnaniiomcrs aT citroncllol (2) as the starting materials.
## Abstract All of the four stereoisomers of 3,13‐dimethylheptadecane (1), the female‐produced sex pheromone of the western false hemlock looper (__Nepytia freemani__), were synthesized by starting from the enatiomers of citronellol (2a) and 2‐methyl‐1‐butanol (4a).
## Abstract The synthesis of four stereoisomers of the female‐produced sex pheromone [(2R,6R,10R)‐, (2S,6R,10R)‐, (2S,6S,10S)‐, and (2R,6S,10S)‐1a] of the rice moth (Corcyra cephalonica) was achieved by starting from (R)‐2a, (R)‐ or (S)‐3a, and (R)‐ or (S)‐4 and using alkylation of alkyl phenyl sul