Fungicidal activity of phenyl N-(4-substituted-phenyl)thionocarbamates

Thirteen phenyl N-(4-substituted-phenyl)thionocarbamates [(4-X-C6H4)NHC(S)OC6H5] were synthesized, and their activities as spore germination inhibitors of Alternaria brassicicola, Botrytis cinerea, Septoria nodorum, and Uromyces viciae-fabae and as protectants against Puccinia recondita on wheat see...

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Bibliographic Details
Published in:Journal of agricultural and food chemistry 1995-08, Vol.43 (8), p.2260-2261
Main Authors: Albores-Velasco, Martha, Thorne, John, Wain, Ralph L
Format: Article
Language:English
Subjects:
ALTERNARIA BRASSICICOLA
Biological and medical sciences
BOTRYTIS CINEREA
Chemical control
Control
ESPORAS
FONGICIDE
Fundamental and applied biological sciences. Psychology
Fungal plant pathogens
FUNGICIDAS
GERMINACION
GERMINATION
LEPTOSPHAERIA NODORUM
Phytopathology. Animal pests. Plant and forest protection
PLANTULAS
PLANTULE
PUCCINIA RECONDITA
SPORE
TRITICUM AESTIVUM
UROMYCES VICIAE-FABAE
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Summary:Thirteen phenyl N-(4-substituted-phenyl)thionocarbamates [(4-X-C6H4)NHC(S)OC6H5] were synthesized, and their activities as spore germination inhibitors of Alternaria brassicicola, Botrytis cinerea, Septoria nodorum, and Uromyces viciae-fabae and as protectants against Puccinia recondita on wheat seedlings were determined. High fungicidal activity was found in thionocarbamates substituted with electron-withdrawing groups or the OH group. Results are discussed on the basis of the physicochemical properties of the thionocarbamates
ISSN:0021-8561
1520-5118
DOI:10.1021/jf00056a054