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 AbstractBiorational approaches for insect control by enzymatic inhibition    Next AbstractA new FT-IR method combined with multivariate analysis for the classification of vinegars from different raw materials and production processes »

J Agric Food Chem


Title:"Enantioselective Synthesis and Activity of All Diastereoisomers of ( E)-Phytal, a Pheromone Component of the Moroccan Locust, Dociostaurus maroccanus"
Author(s):Guerrero A; Ramos VE; Lopez S; Alvarez JM; Dominguez A; Coca-Abia MM; Bosch MP; Quero C;
Address:"Department of Biological Chemistry and Molecular Modelling , Institute of Advanced Chemistry of Catalonia (CSIC) , 08034 Barcelona , Spain. Plant Health Department , Centro de Investigacion y Tecnologia Agroalimentaria de Aragon and Instituto Agroalimentario de Aragon-IA2, CITA-Zaragoza University , 50059 Zaragoza , Spain"
Journal Title:J Agric Food Chem
Year:2019
Volume:20181228
Issue:1
Page Number:72 - 80
DOI: 10.1021/acs.jafc.8b06346
ISSN/ISBN:1520-5118 (Electronic) 0021-8561 (Linking)
Abstract:"The Moroccan locust, Dociostaurus maroccanus (Thunberg, 1815) (Orthoptera: Acrididae), is a polyphagous pest capable of inflicting large losses in agriculture under favorable environmental and climatic conditions. Currently, control of the pest relies solely on the application of conventional insecticides that have negative effects on the environment and human safety. In the search for a more rational, environmentally acceptable approach for locust control, we have previously reported that ( Z/ E)-phytal (1) is a male-produced candidate sex pheromone of this acridid. This molecule, with two stereogenic centers at C-7 and C-11, has four different diastereomers along with the Z/ E stereochemistry of the double bond at C-2. In this paper, we present for the first time the enantioselective synthesis of the four diastereomers of ( E)-phytal and their electrophysiological and behavioral activity on males and females. Our results demonstrate that the ( R, R)-phytal is the most active diastereomer in both assays, significantly attracting females in a double-choice Y olfactometer, and confirming the previous chromatographic assignment as component of the sex pheromone of the Moroccan locust"
Keywords:"Aldehydes/*chemical synthesis/chemistry/*pharmacology Animals Diterpenes/*chemical synthesis/chemistry/*pharmacology Female Grasshoppers/drug effects/physiology Male Pheromones/*chemical synthesis/chemistry/*pharmacology Sexual Behavior, Animal/drug effec;"
Notes:"MedlineGuerrero, Angel Ramos, Victoria Elena Lopez, Sergio Alvarez, Jose Maria Dominguez, Aroa Coca-Abia, Maria Milagro Bosch, Maria Pilar Quero, Carmen eng 2018/12/18 J Agric Food Chem. 2019 Jan 9; 67(1):72-80. doi: 10.1021/acs.jafc.8b06346. Epub 2018 Dec 28"

 
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 23-11-2024