摘要:
Carboxamides of the formula I ##STR1## where the substituents have the following meanings: R.sup.1 is unsubstituted or substituted bicycloalkyl, tricycloalkyl or bicycloalkenyl;R.sup.2,R.sup.3 and R.sup.4 are each, independently of one another, hydrogen, or unsubstituted or substituted: alkyl, cycloalkyl, cycloalkenyl or heterocyclyl;Ar is unsubstituted or substituted aryl or hetaryl,but excluding 2-cyano-N-[1-(1-naphthyl)ethyl]-3-phenyl-bicyclo[2.2.1]hept-5-ene-2-carboxamide, a process for their preparation, compositions comprising compounds I and the use of compounds I for preparing the compositions, and further a process for controlling harmful fungi and the use of the compounds I for this purpose.
摘要:
N-heterocyclic compounds I ##STR1## or their salts or N-oxides, wherein A is an N-heterocycle selected from the group consisting of ##STR2## R.sup.1 -R.sup.6, R.sup.24 -R.sup.26 are hydrogen, cyano, nitro, halogen, aminocarbonyl, methylsulfonyl, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, alkoxyalkyl, alkoxycarbonyl, aryl or aryloxy;m is 0, 1 or 2;Alk is optionally substituted 1,2-ethylidene, 1,3-propylidene cycloalkyl or cycloalkenyl;X is oxygen or sulfur;Q is optionally substituted aryl, cycloalkyl, cycloalkenyl, or arylalkyl;their manufacture and suitable intermediates therefore, as well as compositions comprising them and their use for controlling harmful fungi.
摘要:
Carbamoylcarboxamides of the general formula I ##STR1## and their salts (R.sup.1 is unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or an unsubstituted or substituted nonaromatic carbo- or heterocycle; R.sup.2 is H or unhalogenated or halogenated alkyl or cycloalkyl; R.sup.3 is unsubstituted or substituted alkyl, cycloalkyl or phenylalkyl; R.sup.4 is H or one of the radicals R.sup.3 or R.sup.3 and R.sup.4, together with the C atom to which they are bonded, are an unsubstituted or substituted carbo- or heterocycle; R.sup.5 independently of these is one of the radicals R.sup.2 ; X independently of one another is hydrogen, unsubstituted or substituted alkyl and/or alkenyl; Y independently of one another and of these is one of the radicals X; p,q independently of one another are 0, 1 or 2; R.sup.6 is halogen, cyano, nitro or unsubstituted or substituted alkyl, alkoxy, alkylthio or an unsubstituted or substituted phenyl group bonded via oxygen or sulfur; r is 0, 1, 2 or 3), and compositions containing them, processes for preparation, and the use of the compounds I and the compositions are described.
摘要翻译:PCT No.PCT / EP95 / 03303 Sec。 371日期1997年3月3日 102(e)1997年3月3日PCT PCT 1995年8月19日PCT公布。 公开号WO96 / 07638 日期:1996年3月14日通式I(I)的氨基甲酰甲酰胺及其盐(R1是未取代或取代的烷基,烯基,炔基,环烷基,环烯基或未取代或取代的非芳族碳 - 或杂环; R2是H或 未卤化或卤代烷基或环烷基; R 3为未取代或取代的烷基,环烷基或苯基烷基; R 4为H或R 3或R 3和R 4中的一个与它们所键合的C原子一起为未取代或取代的碳 - 或杂环; R 5独立地为基团R 2; X彼此独立地为氢,未取代或取代的烷基和/或烯基; Y彼此独立地且这些基团为基团X; p,q独立地为 R 1为0,1或2; R 6为卤素,氰基,硝基或未取代或取代的烷基,烷氧基,烷硫基或未经取代或取代的通过氧或硫键合的苯基; r为0,1,2或3) 和组成 包含它们,制备方法以及化合物I和组合物的用途。
摘要:
Quinolines of the formula I ##STR1## where the substituents are as defined herein, the corresponding N-oxides and acid addition salts, a process for their preparation, fungicidal compositions, and their use for controlling harmful fungi.
摘要:
Carbamoylcarboxamides of the general formula I ##STR1## (R.sup.1 =unsubstituted or substituted alkyl, alkenyl, alkynyl; R.sup.2 =hydrogen, halogen, cyano, nitro, or unsubstituted or substituted alkyl, alkoxy, alkylthio, or an unsubstituted or substituted phenyl group which is bonded via oxygen or sulfur) and compositions comprising them, processes for their preparation, and the use of the compounds I and of the compositions.
摘要:
Benzamidoxime derivatives of the formula I: where R1 is difluoromethyl or trifluoromethyl R2 is hydrogen or fluorine R3 is C1-C4-alkyl which may be substituted by cyano, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, C3-C8-cycloalkyl-C1-C4-alkyl R4 is phenyl-C1-C6-alkyl which may carry one or more substitutents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the phenyl ring, or is thienyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the thienyl ring, or is pyrazolyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the pyrazole ring, are prepared, and intermediates for their preparation and their use as fungicides are described.
摘要:
The present invention relates to carbomoylcarboxamide oximes of the formula (I): ##STR1## or salts thereof, processes for preparing the carbomoylcarboxamide oximes, compositions containing the carbomoylcarboxamide oximes and processes for controlling harmful fungi with an effective amount of the carbomoylcarboxamide oximes.
摘要:
Benzamidoxime derivatives of the formula I where R1 is difluoromethyl or trifluoromethyl R2 is hydrogen or fluorine R3 is C1-C4-alkyl which may be substituted by cyano, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, C3-C8-cycloalkyl-C1-C4-alkyl R4 is phenyl-C1-C6-alkyl which may carry one or more substitutents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the phenyl ring, or is thienyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the thienyl ring, or is pyrazolyl-C1-C4-alkyl which may carry one or more substituents selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy on the pyrazole ring, are prepared, and intermediates for their preparation and their use as fungicides are described.
摘要:
The invention relates to benzamidoxim derivatives of formula (I) wherein the substituents have the following meanings: R1 represents difluoromethyl or trifluoromethyl, R2 represents hydrogen or fluorine, R3 represents C1-C4 alkyl optionally substituted with cyano, C1-C4 halogenalkyl, C1-C4 alkoxy-C1-C4 alkyl, C3-C6 alkenyl, C3-C6 halogenalkenyl, C3-C6 alkinyl, C3-C8 cycloalkyl-C1-C4 alkyl, R4 represents phenyl-C1-C6 alkyl, which can carry one or more substituents selected from the group composed of halogen, C1-C4 alkyl, C1-C4 halogenalkyl, C1-C4 alkoxy or C1-C4 halogenalkoxy on the phenyl ring, or thienyl-C1-C4 alkyl, which can carry one or more substituents selected from the group composed of halogen, C1-C4 alkyl, C1-C4 halogenalkyl, C1-C4 halogenalkoxy on the thienyl ring, or pyrazol-C1-C4 alkyl, which can carry one or more substituents selected from the group composed of halogen, C1-C4 alkyl, C1-C4 halogenalkyl, C1-C4 alkoxy or C1-C4 halogenalkoxy on the pyrazol ring. The invention also relates to intermediate products for the preparation of these derivatives and to their use as fungicides.
摘要:
The present invention relates to novel cycloalkylalkane-carboxamides of the formula I where the substituents have the following meanings: A is C3-C6-cycloalkyl; R1 is C1-C6-alkyl or C2-C6-alkenyl; R2, R3 and R4 are hydrogen or, independently of this meaning, have one of the meanings of the radical R1; n is 0 or 1; Y is cyano or halogen; w is phenyl, naphthyl or heteroaryl.