Pheromone synthesis, CXXV. Synthesis of the four possible stereoisomers of 3,7-dimethylnonadecane, the female sex pheromone of Agromyza frontella Rondani-Reference-Cited by-同舟云学术

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

Published:1991-03-12 Issue:3 Volume:1991 Page:213-217
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Mori Kenji,Wu Jiang

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference13 articles.

1. Synthesis of both the enantiomers of hauptmann's periplanone-A and clarification of the structure of Persoons's periplanone-A

2. Identification of female sex pheromone in alfalfa blotch leafminer,Agromyza frontella (Rondani)(Diptera: Agromyzidae)

3. unpublished results.

4. Revision of the absolute configuration of a-factor

5. Pheromone synthesis. Part 76. Synthesis of the enantiomers of 14-methyl-1-octadecene, the sex pheromone of the peach leafminer moth.

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