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Stereoselective synthesis of a sex attractant of the codling moth

✍ Scribed by C. Descoins; C.A. Henrick

Book ID
108384436
Publisher
Elsevier Science
Year
1972
Tongue
French
Weight
171 KB
Volume
13
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES

A stereoselective synthesis of a propose
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McDonough and coworkers have recently isolated' from the Codling Moth, Laspeyresia pomonella (L.), a compound believed to be (22,6E)-7-methyl-5-propyl-2,6-decadien-l-o1 (L) and have reported evidence suggesting that it is a component of the sex pheromone. A mixture

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Disparlure, cis-7,8-epoxy-2-methyloctadecane, was identified as the female-produced sex pheromone of the gypsy moth, Lymantria &spur L., by Bierl, Beroza and Collier.' The 7R,BS enantiomer of disparlure was synthesized by Marumo' and Mori 3 and found to be more attractive to males than the racemate.

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