Acidic derivatives of the fungicide fenpiclonil: effect of adding a methyl group to the N-substituted chain on systemicity and fungicidal activity
✍ Scribed by Jean-François Chollet; Françoise Rocher; Cyril Jousse; Céline Delétage-Grandon; Georges Bashiardes; Jean-Louis Bonnemain
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 174 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1526-498X
- DOI
- 10.1002/ps.977
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✦ Synopsis
Abstract
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. Copyright © 2004 Society of Chemical Industry