𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Pheromone synthesis, CXXXI. Synthesis of the four stereoisomers of 6,10,13-trimethyl-1-tetradecanol, the aggregation pheromone of predatory stink bug,Stiretrus anchorago

✍ Scribed by Mori, Kenji ;Wu, Jiang


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
601 KB
Volume
1991
Category
Article
ISSN
0947-3440

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The synthesis of the four stereoisomers of 6,10,13‐trimethyl‐1‐tetradecanol (1a), the male‐produced aggregation pheromone of the predatory stink bug Stiretrus anchorago, was achieved by starting from (R)‐citronellol (2a), methyl (R)‐ or (S)‐3‐hydroxy‐2‐methylpropanoate (10) and 4‐chloro‐1‐butanol (12a).


📜 SIMILAR VOLUMES


Pheromone Synthesis, CLXVII. Synthesis o
✍ Mori, Kenji ;Murata, Noriaki 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 917 KB

## Abstract All of the eight possible stereoisomers of methyl 2,6,10‐trimethyltridecanoate (1), the male‐produced attractant pheromone of the South American soybean pest, __Euschistus heros__, and that of __E. obscurus__, are synthesized by starting from the enantiomers of citronellol (2) and methy

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