## 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, 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
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✦ 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).
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## 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