2006
DOI: 10.1271/bbb.70.508
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and Characterization of 3,13- and 2,13-Octadecadienyl Compounds for Identification of the Sex Pheromone Secreted by a Clearwing Moth,Nokona pernix

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

1
24
0

Year Published

2007
2007
2021
2021

Publication Types

Select...
7

Relationship

3
4

Authors

Journals

citations
Cited by 23 publications
(25 citation statements)
references
References 15 publications
1
24
0
Order By: Relevance
“…In addition, we identified another dienyl acetate as a third component; therefore, field evaluation of the synthetic pheromones was carried out by focusing upon the activity of the geometrical isomers of the 3,13-dienyl acetates and the effect of the third component on the activity of the conventional two-component lure. In addition, we examined the effects on attractiveness of male S. hector by E3,Z13-18:OH or Z3,Z13-18:OH, while these compounds were also important key pheromone compounds for some clearwing species (Naka et al, 2006;Ando, 2008).…”
mentioning
confidence: 99%
“…In addition, we identified another dienyl acetate as a third component; therefore, field evaluation of the synthetic pheromones was carried out by focusing upon the activity of the geometrical isomers of the 3,13-dienyl acetates and the effect of the third component on the activity of the conventional two-component lure. In addition, we examined the effects on attractiveness of male S. hector by E3,Z13-18:OH or Z3,Z13-18:OH, while these compounds were also important key pheromone compounds for some clearwing species (Naka et al, 2006;Ando, 2008).…”
mentioning
confidence: 99%
“…7,8) Note 3,13-diene and a (2Z,13Z)-isomer of the 2,13-diene. 9) The mass spectra of the two acetates have many aspects of similarity, but the relative intensity between two ions at m=z 248 and 67 of the 3,13-diene is smaller than that of the 2,13-diene. The value for the natural pheromone coincides well with that for the 3,13-diene.…”
mentioning
confidence: 99%
“…The value for the natural pheromone coincides well with that for the 3,13-diene. Since the two positional isomers of octadecadien-1-ol have been more clearly differentiated by their GC-MS data than the isomers of the acetate, 9) the acetate component in the crude extract (5.0 FE) was saponified with K 2 CO 3 , and the resulting alcohol was analyzed by GC-MS. The chromatographic behavior (KI, 2684) and small relative intensity (1%) of the ion at m=z 248 confirmed the 3,13-dienyl structure of the natural pheromone.…”
mentioning
confidence: 99%
See 2 more Smart Citations