Microbial Hydroxylation of the Herbicide N-(3,4-Dichlorophenyl)methacrylamide (Dicryl)

Peter R. Wallnöfer; Steve Safe; Otto Hutzinger

doi:10.1021/jf60187a047

Microbial Hydroxylation of the Herbicide N-(3,4-Dichlorophenyl)methacrylamide (Dicryl)

Peter R. Wallnöfer, Steve Safe, Otto Hutzinger

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

The fungus Rhizopus japonicus converts the herbicide N-(3,4-dichlorophenyl)methacrylamide (dicryl) to N-3,4-dichlorophenyl)-2-methyl-2,3-dihydroxypropionamide. This metabolite was formed by the addition of two hydroxyl groups to the ethylenic double bond of dicryl. Its structure was elucidated by nuclear magnetic resonance and mass spectrometric analysis.

Original language	English (US)
Pages (from-to)	502-504
Number of pages	3
Journal	Journal of Agricultural and Food Chemistry
Volume	21
Issue number	3
DOIs	https://doi.org/10.1021/jf60187a047
State	Published - May 1 1973

ASJC Scopus subject areas

Chemistry(all)
Agricultural and Biological Sciences(all)

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title = "Microbial Hydroxylation of the Herbicide N-(3,4-Dichlorophenyl)methacrylamide (Dicryl)",

abstract = "The fungus Rhizopus japonicus converts the herbicide N-(3,4-dichlorophenyl)methacrylamide (dicryl) to N-3,4-dichlorophenyl)-2-methyl-2,3-dihydroxypropionamide. This metabolite was formed by the addition of two hydroxyl groups to the ethylenic double bond of dicryl. Its structure was elucidated by nuclear magnetic resonance and mass spectrometric analysis.",

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year = "1973",

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T1 - Microbial Hydroxylation of the Herbicide N-(3,4-Dichlorophenyl)methacrylamide (Dicryl)

AU - Wallnöfer, Peter R.

AU - Safe, Steve

AU - Hutzinger, Otto

PY - 1973/5/1

Y1 - 1973/5/1

N2 - The fungus Rhizopus japonicus converts the herbicide N-(3,4-dichlorophenyl)methacrylamide (dicryl) to N-3,4-dichlorophenyl)-2-methyl-2,3-dihydroxypropionamide. This metabolite was formed by the addition of two hydroxyl groups to the ethylenic double bond of dicryl. Its structure was elucidated by nuclear magnetic resonance and mass spectrometric analysis.

AB - The fungus Rhizopus japonicus converts the herbicide N-(3,4-dichlorophenyl)methacrylamide (dicryl) to N-3,4-dichlorophenyl)-2-methyl-2,3-dihydroxypropionamide. This metabolite was formed by the addition of two hydroxyl groups to the ethylenic double bond of dicryl. Its structure was elucidated by nuclear magnetic resonance and mass spectrometric analysis.

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ER -

Microbial Hydroxylation of the Herbicide N-(3,4-Dichlorophenyl)methacrylamide (Dicryl)

Abstract

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