1982
DOI: 10.1271/bbb1961.46.2283
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1,3,5,7-Tetramethyldecyl formate, lardolure: Aggregation pheromone of the acarid mite, Lardoglyphus konoi (sasa et asanuma) (Acarina: Acaridae).

Abstract: From an acarid mite, Lardoglyphus konoi (Sasa et Asanuma) (Acarina: Acaridae), with its culture medium,an aggregation pheromonewas isolated. The structure of the pheromonewas determined as 1,3,5,7-tetramethyldecyl formate and identified by 1 1 steps of organic synthesis. The absolute configuration of Q was assigned as R. The compound has been assigned the trivial name lardolure. The synthesized diastereomeric mixture of racemates showed one-tenth of the activity of the natural pheromone against the test mite, … Show more

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Cited by 32 publications
(10 citation statements)
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“…These eluted as the first two peaks in GC, thus confirming the 4,6‐ syn arrangement in the natural 8 . In the mite Lardoglyphus konoi , the related aggregation pheromone lardolure 15 has the all‐ R configuration 15. We therefore chose to synthesize a pure enantiomer of (4 R ,6 R ,8 R )‐ 8 in order to compare it with the natural product.…”
Section: Resultsmentioning
confidence: 99%
“…These eluted as the first two peaks in GC, thus confirming the 4,6‐ syn arrangement in the natural 8 . In the mite Lardoglyphus konoi , the related aggregation pheromone lardolure 15 has the all‐ R configuration 15. We therefore chose to synthesize a pure enantiomer of (4 R ,6 R ,8 R )‐ 8 in order to compare it with the natural product.…”
Section: Resultsmentioning
confidence: 99%
“…Parts of these compounds function as alarm, aggregation or sex pheromones (Kuwahara et al 1975(Kuwahara et al , 1982Leal et al 1989a). The profile of secretion has been found to be characteristic for each species, and provides a chemical key which can be used to confirm the identification of a given species based on conventional morphological characters (Leal et al 1989b;Kuwahara 1999).…”
Section: Introductionmentioning
confidence: 99%
“…Lardoglyphus konoi Sasa et Asanuma provided an exception, having an aggregation pheromone, lardolure (1R,3R,5R,7R-1,3,5,7-tetramethyldecyl formate) (Kuwahara et al 1982;Mori and Kuwahara 1986a, b), and an alarm pheromone, neral [3,7-dimethyl-(Z)-2,6-octadienal] (Kuwahara et al 1980). The alarm pheromone is produced from the opisthonotal glands, whereas evidence has suggested that lardolure is produced from another internal source (Kuwahara 2004).…”
Section: Introductionmentioning
confidence: 99%