Abstract
IN this Department previous investigations1,2 of the metabolic fate of a series of chlorinated phenoxyacetic acids in stem tissues of Avena sativa have demonstrated that the formation of glucose esters or hydroxylation followed by conversion to a glucoside are major pathways. In this tissue 2,4-dichlorophenoxyacetic acid (2,4-D) is converted principally into 1-0-(2,4-dichlorophenoxyacetyl)-β-D-glucose. In contrast, in the stems of Phaseolus vulgaris the principal metabolite isolated was seemingly a glucoside of a phenolic acid3 which was not a hydroxy-2,4-dichlorophenoxyacetic acid3–5. Further investigation has identified the presence of a mixture of 2,5-dichloro-4-hydroxyphenoxyacetic acid and 2,3-dichloro-4-hydroxyphenoxyacetic acid.
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References
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Conant, J. B., and Fieser, L. F., J. Amer. Chem. Soc., 45, 2204 (1923).
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THOMAS, E., LOUGHMAN, B. & POWELL, R. Metabolic Fate of 2,4-Dichlorophenoxyacetic Acid in the Stem Tissue of Phaseolus vulgaris. Nature 204, 884–885 (1964). https://doi.org/10.1038/204884a0
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DOI: https://doi.org/10.1038/204884a0
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