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- W2497785557 endingPage "79" @default.
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- W2497785557 abstract "Herbicidal activity and non-target toxicity may be drastically different between enantiomers of a chiral herbicide. The enantiomers of chiral herbicides are usually separated and analyzed by chromatographic methods such as high-performance liquid chromatography (HPLC), gas chromatography (GC), supercritical fluid chromatography (SFC), and capillary electrophoresis (CE). Several chromatographic techniques are used for preparing pure-enantiomer herbicides. Some chiral herbicides have been commercialized with the pure active enantiomer, such as 1′S-metolachlor (aSS, aRS), quizalofop-p-ethyl, haloxyfop-p-methyl, fluazifop-p-butyl, (R)-napropamide, etc." @default.
- W2497785557 created "2016-08-23" @default.
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- W2497785557 date "2011-01-01" @default.
- W2497785557 modified "2023-09-26" @default.
- W2497785557 title "Enantioselective Separation and Analysis of Chiral Herbicides" @default.
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- W2497785557 doi "https://doi.org/10.1021/bk-2011-1085.ch004" @default.
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