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 Abstract"Isolation, identification, and synthesis of male-produced sex pheromone of papaya fruit fly,Toxotrypana curvicauda Gerstaecker (Diptera: Tephritidae)"    Next Abstract"The effect of salt concentrations on the fermentation of doenjang, a traditional Korean fermented soybean paste" »

J Chem Ecol


Title:"Conformational analysis of serricornin: Application of molecular mechanics calculations to stereochemical assignment of serricornin, sex pheromone of cigarette beetle (Lasioderma serricorne F.)"
Author(s):Chuman T; Shimazaki K; Mori M; Okada K; Goto H; Osawa E; Sakakibara K; Hirota M;
Address:"Life Science Research Laboratory, Japan Tobacco Inc., 6-2 Umegaoka, Midori-ku, 227, Yokohama, Japan"
Journal Title:J Chem Ecol
Year:1990
Volume:16
Issue:10
Page Number:2877 - 2888
DOI: 10.1007/BF00979480
ISSN/ISBN:0098-0331 (Print) 0098-0331 (Linking)
Abstract:"Conformational analysis using molecular mechanics (MM) was performed for a determination of the stereochemistry of serricornin, the sex pheromone of the cigarette beetle (Lasioderma serricorne F.). An exhaustive conformational analysis using MM2 calculations with algorithms for covering torsional energy surfaces of flexible molecules furnishes coordinates and steric energies of all local energy minimum conformers of serricornin, both acyclic and the corresponding cyclic forms. These coordinates gave angles required for the calculation of vicinal H/H coupling constants ((3) J HHs) of each energy minima by Altona's modified Karplus equation. The Boltzmann distributions of all local energy minima were calculated from their steric energies to furnish populations of each energy minimum conformer. Populationweighted averaged(3) J HHs of four enantiomeric pairs, (S (*),S (*),S (*))-, (S (*),S (*),R (*))-, (S (*),R (*),S (*))-, and (R (*),S (*),S (*))-serricornins were calculated from the data above. The observed(3) J HHs of the naturally occurring serricornin, both acyclic and cyclic forms, are fitted best to calcd.(3) J HHs of (4S (*), 6S (*), 7S (*))-acyclic and (3S (*), 5S (*), 6S (*))-cyclic serricornin, respectively, among those of four enantiomeric pairs of serricornin"
Keywords:
Notes:"PubMed-not-MEDLINEChuman, T Shimazaki, K Mori, M Okada, K Goto, H Osawa, E Sakakibara, K Hirota, M eng 1990/10/01 J Chem Ecol. 1990 Oct; 16(10):2877-88. doi: 10.1007/BF00979480"

 
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 05-12-2024