Synthesis of tritiated derivatives of the diphenylether herbicides acifluorfen and acifluorfen methyl
✍ Scribed by René Mornet; Lucien Gouin; Michel Matringe; René Scalla; Colin Swithenbank
- Book ID
- 102375819
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- French
- Weight
- 336 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Acifluorfen 1 and acifluorfen methyl 2, two herbicides of the diphenylether family, are inhibitors of protoporphyrinogen oxidases. Two tritiated derivatives of these compounds, namely 3‐[^3^H]‐5‐[2‐chloro‐4‐(trifluoromethyl)phenoxy]‐2‐nitrobenzoic acid [^3^H]‐1, and methyl 3‐[^3^H]‐5‐[2‐chloro‐4‐(trifluoromethyl)phenoxy]‐2‐nitrobenzoic acid [^3^H]‐2, have been synthesised from 3‐[^3^H]‐5‐hydroxybenzoic acid, in order to probe their interactions with the target enzymes.
📜 SIMILAR VOLUMES
Polyclonal and monoclonal antibodies reactive with aciÑuorfen (AF) were prepared by the immunization of, respectively, rabbits and mice with AFbovine serum albumin conjugates. The reactivities of polyclonal antibody and three monoclonal antibodies (AF 9-1, AF 51-5 and AF 75-144) were examined in an