1995
DOI: 10.1021/jf00055a035
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Kinetics and mechanisms of hydrolysis of dicarboximide fungicides in micellar media

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Cited by 9 publications
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“…In nonionic micelles, the loss of the ethyl ester group and the opening of a dihydrocarbon ring will be inhibited. In the alkaline hydrolysis of benzoic acid and benzyl fungicides, the degradation mechanism was inferred to be a carboxyl fracture (Figures 2(f )-2(k)) [79][80][81][82].…”
Section: Fungicidementioning
confidence: 99%
“…In nonionic micelles, the loss of the ethyl ester group and the opening of a dihydrocarbon ring will be inhibited. In the alkaline hydrolysis of benzoic acid and benzyl fungicides, the degradation mechanism was inferred to be a carboxyl fracture (Figures 2(f )-2(k)) [79][80][81][82].…”
Section: Fungicidementioning
confidence: 99%