𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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


Pheromone synthesis, CIX. Synthesis of t
✍ Mori, Kenji ;Igarashi, Yasuhiro 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 406 KB

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.

Pheromone Synthesis, CLXXVI. Synthesis o
✍ Takikawa, Hirosato ;Shirai, Yasuo ;Kobayashi, Makoto ;Mori, Kenji 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 621 KB

## 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).

Pheromone synthesis, CXXVI. Synthesis an
✍ Mori, Kenji ;Harada, Hironori ;Zagatti, Pierre ;Cork, Alan ;Hall, David R. 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 870 KB

## 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