𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and Biological Activity of Methyl 2,6,10-Trimethyldodecanoate and Methyl 2,6,10-Trimethyltridecanoate: Male-Produced Sexual Pheromones of Stink Bugs Euschistus heros and Piezodorus guildinii

✍ Scribed by Paulo H. G. Zarbin; Aurélia Reckziegel; Ernst Plass; Miguel Borges; Wittko Francke

Book ID
111561970
Publisher
Springer
Year
2000
Tongue
English
Weight
141 KB
Volume
26
Category
Article
ISSN
0098-0331

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Pheromone Synthesis, CLXII. Synthesis of
Pheromone Synthesis, CLXII. Synthesis of Methyl 2,6,10-Trimethyltridecanoate, the Male-Produced Pheromone of the Stink Bugs,Euschistus heros andE. obscurus, as a Stereoisomeric Mixture
✍ Mori, Kenji ;Murata, Noriaki 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 252 KB

## Abstract Methyl 2,6,10‐trimethyltridecanoate (1), the male‐produced attractant pheromone of the South American soybean pest, __Euschistus heros__, and that of __E. obscurus__, was synthesized as a stereoisomeric mixture and identified by a comparison with the natural product on the basis of GC a

Pheromone Synthesis, CLXVII. Synthesis o
Pheromone Synthesis, CLXVII. Synthesis of All of the Eight Stereoisomers of Methyl 2,6,10-Trimethyltridecanoate, the Male-Produced Pheromone of the Stink Bugs,Euschistus heros andE. obscurus
✍ 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 syntheses: A tropical approach
Pheromone syntheses: A tropical approach. Enantioselective synthesis of the (2R,6S,10S) and (2S,6S,10S) isomers of methyl 2,6,10-trimethyldodecanoate
✍ J.Tércio B. Ferreira; Paulo H.G. Zarbin 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 622 KB

The enantioselective syntheses of two stereoisomers, (2R,6S,10S) and (2S,6S,10S), of methyl 2,6,10-trimethyldodecanote, out of eight possible isomers, are described , employing the stereoselective hydroboration of (-)-isopulegol (2) and (+)-neo-isopulegol (2a) as the key reaction.

Pheromone synthesis, CXXVI. Synthesis an
Pheromone synthesis, CXXVI. Synthesis and biological activity of four stereoisomers of 6,10,14-trimethyl-2-pentadecanol, the female-produced sex pheromone of rice moth (Corcyra cephalonica)
✍ 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