Document Detail


Acidic derivatives of the fungicide fenpiclonil: effect of adding a methyl group to the N-substituted chain on systemicity and fungicidal activity.
MedLine Citation:
PMID:  15751009     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A new acidic derivative of the fungicide fenpiclonil was synthesized containing a methyl group on the alpha-position of the carboxyl function of N-carboxymethyl-3-cyano-4-(2,3-dichlorophenyl)pyrrole. The phloem mobility of the resulting N-(1-carboxyethyl)-3-cyano-4-(2,3-dichlorophenyl)pyrrole was comparable with that of the former compound, but was higher at external pH 5.0. Unlike the derivatives previously synthesized, it was comparable with fenpiclonil in its fungicidal activity against the pathogenic fungus Eutypa lata.
Authors:
Jean-François Chollet; Françoise Rocher; Cyril Jousse; Céline Delétage-Grandon; Georges Bashiardes; Jean-Louis Bonnemain
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Pest management science     Volume:  61     ISSN:  1526-498X     ISO Abbreviation:  Pest Manag. Sci.     Publication Date:  2005 Apr 
Date Detail:
Created Date:  2005-03-15     Completed Date:  2005-06-28     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  100898744     Medline TA:  Pest Manag Sci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  377-82     Citation Subset:  IM    
Copyright Information:
Copyright 2004 Society of Chemical Industry.
Affiliation:
Laboratoire Synthèse et Réactivité des Substances Naturelles, Unité Mixte de Recherche CNRS 6514, 40, av du Recteur Pineau, 86022 Poitiers cedex, France.
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MeSH Terms
Descriptor/Qualifier:
Ascomycota
Fungicides, Industrial / chemistry*,  metabolism
Hydrogen-Ion Concentration
Molecular Structure
Pyrroles / chemistry*,  metabolism
Ricinus / metabolism
Structure-Activity Relationship
Chemical
Reg. No./Substance:
0/Fungicides, Industrial; 0/Pyrroles; 0/fenpiclonil

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