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 AbstractSeasonal Dispersal of the Oak Wilt Fungus by Colopterus truncatus and Carpophilus sayi in Minnesota    Next Abstract"Transverse approach between real world concentrations of SO2, NO2, BTEX, aldehyde emissions and corrosion in the Grand Mare tunnel" »

J Org Chem


Title:Stereoselective synthesis of trifluoro- and monofluoro-analogues of frontalin and evaluation of their biological activity
Author(s):Ambrosi P; Arnone A; Bravo P; Bruche L; De Cristofaro A; Francardi V; Frigerio M; Gatti E; Germinara GS; Panzeri W; Pennacchio F; Pesenti C; Rotundo G; Roversi PF; Salvadori C; Viani F; Zanda M;
Address:"CNR, Centro di Studio sulle Sostanze Organiche Naturali, via Mancinelli 7, I-20131 Milano, Italy"
Journal Title:J Org Chem
Year:2001
Volume:66
Issue:25
Page Number:8336 - 8343
DOI: 10.1021/jo0055640
ISSN/ISBN:0022-3263 (Print) 0022-3263 (Linking)
Abstract:"The stereoselective synthesis of both enantiomers of trifluoro frontalin (-)-(1S,5R)- and (+)-(1R,5S)-8, as well as of diastereomeric monofluoro frontalines (-)-(1R,2R,5R)-18 and (-)-(1R,2S,5R)-20, analogues of the bioactive component of the aggregation pheromone of the Scolytidae insect family, has been accomplished starting from (-)-(1R)- and (+)-(1S)-menthyl (S)-toluene-4-sulfinate as a source of chirality and methyl trifluoroacetate or fluoroacetate, respectively, as sources of fluorine. The C-1 stereocenters were installed via stereoselective epoxidation of beta-sulfinyl ketones 2 and 13 with diazomethane. The bicyclic core was obtained by totally stereocontrolled and chemoselective tandem Wacker oxidation/intramolecular ketalization of the intermediate unsatured sulfinyl diols 5, 15, and 19. Axially fluorinated (-)-20 elicited a strong electroantennographic response in laboratory tests on females of Dendroctonus micans, whereas equatorially fluorinated (-)-18 and the trifluoroanalogue (-)-8 showed modest responses. Field trials using (-)-20 were not indicative owing to the locally scarce population of D. micans, but it showed some attractiveness for other Coleoptera families"
Keywords:"Animals Behavior, Animal/drug effects Bridged Bicyclo Compounds, Heterocyclic/*chemical synthesis/chemistry Coleoptera Electrophysiology Female Fluorine Indicators and Reagents Insect Control Pheromones/*antagonists & inhibitors/biosynthesis Sense Organs;"
Notes:"MedlineAmbrosi, P Arnone, A Bravo, P Bruche, L De Cristofaro, A Francardi, V Frigerio, M Gatti, E Germinara, G S Panzeri, W Pennacchio, F Pesenti, C Rotundo, G Roversi, P F Salvadori, C Viani, F Zanda, M eng Research Support, Non-U.S. Gov't 2001/12/12 J Org Chem. 2001 Dec 14; 66(25):8336-43. doi: 10.1021/jo0055640"

 
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 16-11-2024