Uso de compuestos de ditiina-tetracarboximidas que sirven para combatir hongos fitopatogenos; procedimiento para combatir dichos hongos; compuestos de ditiina-tetracarboximidas; uso de compuestos de ditiina-diisoimidas; y compuestos ditiina-diisoimidas

USO DE COMPUESTOS DE D(TIINA-TETRACARBOXIMIDAS QUE SIRVEN PARA COMBATIR HONGOS FITOPATÓGENOS: PROCEDIMIENTO PARA COMBATIR DICHOS HONGOS; COMPUESTOS DE DITIINA-TETRACARBOXIMIDAS; USO DE COMPUESTOS DE DITIINA-DIISOIMIDAS; Y COMPUESTOS DITIINA-DIISOIMIDAS. Use of dithiin-tetracarboximide compounds (I)...

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Main Authors DAHMEN, PETER, VOERSTE, ARND, SEITZ, THOMAS, DUNKEL, RALF, TIETJEN, KLAUS-GÜNTHER, WACHENDORFF-NEUMANN, ULRIKE, BENTING, JÜRGEN, HILLEBRAND, STEFAN
Format Patent
LanguageSpanish
Published 29.07.2011
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Summary:USO DE COMPUESTOS DE D(TIINA-TETRACARBOXIMIDAS QUE SIRVEN PARA COMBATIR HONGOS FITOPATÓGENOS: PROCEDIMIENTO PARA COMBATIR DICHOS HONGOS; COMPUESTOS DE DITIINA-TETRACARBOXIMIDAS; USO DE COMPUESTOS DE DITIINA-DIISOIMIDAS; Y COMPUESTOS DITIINA-DIISOIMIDAS. Use of dithiin-tetracarboximide compounds (I) and dithiin-diisoimide compounds (V) for treating phytopathogenic fungi, is claimed. Use of dithiin-tetracarboximide compounds of formula (I) and dithiin-diisoimide compounds of formula (V) for treating phytopathogenic fungi, is claimed. R 1>, R 2> : H, 1-8C-alkyl (optionally substituted by halo, OR 3> or COR 4>), 3-7C-cycloalkyl (optionally substituted by halo, 1-4C-alkyl or 1-4C-haloalkyl), aryl (optionally substituted by halo, 1-4C-alkyl, 1-4C-haloalkyl, COR 4> or sulfonylamino) or aryl-(1-4C-alkyl); R 3> : H, 1-4C-alkyl, 1-4C-alkyl carbonyl or aryl (optionally substituted by halo, 1-4C-alkyl or 1-4C-haloalkyl); R 4> : OH, 1-4C-alkyl or 1-4C-alkoxy; and n : 0 or 1. Independent claims are included for: (1) an agent for combating phytopathogenic fungi comprising (I), diluents and/or surface active materials; (2) the dithiin-tetracarboximide compounds of formula (Ic); and (3) the dithiin-diisoimide compounds of formula (Va). R1a, R2a : 1-8C-alkyl substituted by F, OR3a or COR4a, 3-7C-cycloalkyl substituted by halo, 1-4C-alkyl or 1-4C-haloalkyl, or aryl-(1-4C-alkyl) substituted by COR4a in alkyl portion, preferably 1-4C-alkyl (optionally substituted by F, OH, CH 3O, C 2H 5O, methylcarbonyloxy, or carboxyl), 3-7C-cycloalkyl (optionally substituted by Cl, CH 3 or CF 3), 1-phenethyl or 2-phenethyl; R3a : 1-4C-alkyl, 1-4C-alkylcarbonyl or aryl (optionally substituted by halo, 1-4C-alkyl or 1-4C-haloalkyl), preferably CH 3, methylcarbonyl or phenyl; R4a : OH, 1-4C-alkyl or 1-4C-alkoxy, preferably OH or CH 3O; and r : 0 (preferred) or 1. Where R1a and R2a are not simultaneously acetoxymethyl (preferred) or methoxymethyl. [Image] [Image] ACTIVITY : Fungicide; Nematocide; Anthelmintic; Insecticide; Acaricide; Antibacterial; Virucide. MECHANISM OF ACTION : None given.
Bibliography:Application Number: CL20110000603