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The D- and L-enantiomers of the wild oat herbicide diclofop-methyl (title compound) were prepared utilizing resolution operations and by synthetic routes with optically active compounds as starting material. The dextro-rotatory product which the D(R)-configuration can be attributed to, was found to be the herbicidally active species.

zeitschrift für naturforschung b

Synthese und herbizide Wirksamkeit der D- und L-Enantiomeren des 2- [4-(2.4-Dichlorphenoxy)-phenoxy] -propionsäure-methylesters / Synthesis and Herbicidal Activity of the D- and L-Methyl 2-[4-(2,4-Dichlorophenoxy)-phenoxy]-propionate Enantiomers