Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractStimulation of the biosynthesis of the antibiotics lambertellols by the mycoparasitic fungus Lambertella corni-maris under the acidic conditions produced by its host fungus in vitro    Next AbstractTarget regulation of V2R expression and functional maturation in vomeronasal sensory neurons in vitro »

J Chem Ecol


Title:"Synthesis and field evaluation of stereoisomers and analogues of 5-methylheptadecan-7-ol, an unusual sex pheromone component of the lichen moth, Miltochrista calamina"
Author(s):Muraki Y; Taguri T; Yamakawa R; Ando T;
Address:"Graduate School of Bio-Applications and Systems Engineering, Tokyo University of Agriculture and Technology, Koganei, Tokyo, 184-8588, Japan"
Journal Title:J Chem Ecol
Year:2014
Volume:20140315
Issue:3
Page Number:250 - 258
DOI: 10.1007/s10886-014-0405-5
ISSN/ISBN:1573-1561 (Electronic) 0098-0331 (Linking)
Abstract:"Females of the lichen moth, Miltochrista calamina (Arctiidae, Lithosiinae), were previously shown to produce 5-methylheptadecan-7-ol (1) as a sex pheromone. In field tests, males were attracted only by the (5R,7R)-isomer of the four stereoisomers that were prepared by separation from two mixtures of diastereoisomers. A new route to (5R,7R)-1 starting from (S)-propylene oxide was developed utilizing the SN2 reaction of an optically active secondary tosylate and the Jacobsen hydrolytic kinetic resolution of an epoxide intermediate as key steps. Enantioselective HPLC analysis of the product and the antipode synthesized from (R)-propylene oxide confirmed their high enantiomeric excess (> 99 %). Using this stereospecific synthesis, six analogues with the same configuration as (5R,7R)-1 but with different alkyl chain(s) connected to the stereogenic centers were prepared in order to obtain GC/MS data and to examine the ability of M. calamina males to discriminate between them. The mass spectra of the synthetic analogues revealed characteristic fragment ions derived by cleavage around the methyl group in addition to that at the hydroxyl group. In field trapping tests, five out of the six compounds were attractive to male M. calamina moths, indicating that the males distinguished the configurations of methyl and hydroxyl groups but were less able to perceive differences in the lengths of the two alkyl chains in the pheromone"
Keywords:"Animals Behavior, Animal/drug effects Chromatography, High Pressure Liquid Fatty Alcohols/analysis/*chemical synthesis/pharmacology Female Gas Chromatography-Mass Spectrometry Male Moths/*chemistry/metabolism Sex Attractants/*analysis/chemical synthesis/p;"
Notes:"MedlineMuraki, Yuta Taguri, Tomonori Yamakawa, Rei Ando, Tetsu eng Research Support, Non-U.S. Gov't 2014/03/19 J Chem Ecol. 2014 Mar; 40(3):250-8. doi: 10.1007/s10886-014-0405-5. Epub 2014 Mar 15"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 05-07-2024