✦ LIBER ✦

Synthesis of all Four Stereoisomers of Leucomalure, Components of the Female Sex Pheromone of the Satin Moth, Leucoma salicis

✍ Scribed by Shin-etsu Muto; Kenji Mori

Publisher: John Wiley and Sons
Year: 2003
Tongue: English
Weight: 174 KB
Volume: 2003
Category: Article
ISSN: 1434-193X
DOI: 10.1002/ejoc.200390186

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Pheromone Synthesis. Part 219. Synthesis

Pheromone Synthesis. Part 219. Synthesis of All Four Stereoisomers of Leucomalure, Components of the Female Sex Pheromone of the Satin Moth, Leucoma salicis.

✍ Shin-etsu Muto; Kenji Mori 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 60 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Pheromone synthesis, CXXV. Synthesis of

Pheromone synthesis, CXXV. Synthesis of the four possible stereoisomers of 3,7-dimethylnonadecane, the female sex pheromone of Agromyza frontella Rondani

✍ Mori, Kenji ;Wu, Jiang 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 473 KB

## 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).

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

Pheromone Synthesis, CLXXVI. Synthesis o

Pheromone Synthesis, CLXXVI. Synthesis of the Four Stereoisomers of 3,13-Dimethylheptadecane, the Major Sex Pheromone Component of the Western False Hemlock Looper

✍ 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).

Stereospecific Synthesis of all Four Iso

Stereospecific Synthesis of all Four Isomeric 6,8-Heneicosadien-11-ones: Sex Pheromone Components of the Painted Apple Moth Teia anartoides.

✍ Daniel J. Comeskey; Barry J. Bunn; Simon Fielder 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 82 KB 👁 2 views

Pheromone Synthesis, CLXXV.– Synthesis o

Pheromone Synthesis, CLXXV.– Synthesis of Koiganal I and II, the Sex Pheromone Components of the Webbing Clothes Moth

✍ Takikawa, Hirosato ;Takenaka, Motonobu ;Mori, Kenji 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 251 KB

## Abstract Koiganal I [(__E__)‐2‐octadecenal (1)] and II [(2__E__,13__Z__)‐2,13‐octadecadienal (2)], the female‐produced pheromone components of the webbing clothes moth (__Tineola bisselliella__), were synthesized.