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Metabolism and Selectivity of Plant-growth Regulator Herbicides

Abstract

THE inability of the herbicide 4-chloro-2-methyl phenoxyacetic acid (MCPA) to control certain dicotyledonous weeds can be overcome by introducing into the molecule a single α-alkyl substituent1. DL-α-(4-chloro-2-methylphenoxy) propionic acid (CMPP) is now widely used to control Galium aparine (cleavers), an important cornland weed.

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References

  1. Lush, G. B., and Leafe, E. L., Proc. Third British Weed Control Conf., 625 (1956).

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  3. Fang, S. C., and Butts, J. S., Plant Physiol., 29, 56 (1954).

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LEAFE, E. Metabolism and Selectivity of Plant-growth Regulator Herbicides. Nature 193, 485–486 (1962). https://doi.org/10.1038/193485a0

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