Abstract:
The invention relates to benzyl amidoxime derivatives of formula (I) as fungicides wherein: A represents an aryl or heteraryl radical; Y represents a straight-chained or branched C1-C4 alkylene group, whereby a carbon atom can be substituted by an oxygen, nitrogen or sulphur atom or by a cyclopropyl group; Rn represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy; R represents optionally substituted phenyl C1-C6 alkyl, thienyl C1-C4 alkyl, or pyrazolyl C1-C4 alkyl, Rp represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy, C1-C6 alkyl carbonyl; n represents 0-5; and p represents 0-4, according to the number of free valences.
Abstract:
The invention relates to 5-hetaryl-4-pyrimidines of formula (I) and to their salts and plant protection agents which contain at least one compound of said type as an active component, wherein W represents oxygen, sulphur, a group S=O or S(=O) 2 ; R 1 represents optionally substituted C 1 -C 8 -alkyl, C 3 -C 8 -cycloalkyl, C 5 -C 10 -bicycloalkyl, C 2 -C 8 -alkenyl, C 4 -C 10 -alkadienyl, C 3 -C 6 -cycloalkenyl, C 2 -C 8 -alkynyl, phenyl, naphthyl, or a C-bound five- or six-membered saturated, partially unsaturated or aromatic heterocycle containing one, two, three or four heteroatoms from the groups O, N or S as ring members; R 2 represents halogen, cyano, hydroxy, mercapto, N 3 , C 1 -C 6 -alkyl, C 2 -C 8 -alkenyl, C 2 -C 8 -alkynyl, C 1 C 6 -halogenalkyl, C 1 C 6 -alkoxy, C 3 -C 8 -alkenyloxy, C 3 -C 8 -alkynyloxy, C 1 C 6 -halogenalkoxy, C 1 -C 6 -alkylthio, C 3 -C 8 -alkenylthio, C 3 -C 8 -alkynylthio, C 1 -C 6 -halogenalkylthio, or a radical of formulae C(=Z)OR 21 , C(=Z)NR 22 R 23 , C(=Z)NR 24 -NR 22 R 23 , C(=Z)R 25 , CR 26 R 27 -OR 28 , CR 26 R 27 -NR 22 R 23 , ON(=CR 29 R 30 ), O-C(=Z)R 25 , NR 22 R 23a , NR 31 (C(=Z)R 25 ), NR 31 (C(=Z)OR 21 ), NR 31 (C(=Z)-NR 22 R 23 ), NR 32a (N=CR 29 R 30 ), NR 32 NR 22 R 23 , NR 32 OR 21 , or C(=N-Z'-R 25 )SR 21 ; or a cyclic radical; R3 represents hydrogen, OH, halogen, cyano, NR 37 R 38 , C 1 -C--alkyl, C 1 -C 8 -alkoxy, C 1 -C 8 -alkylthio, C 1 -C 8 -alkylsulfinyl, C 1 -C--alkylsulfonyl, C 2 -C 8 -alkenyl or C 2 -C 8 -alkinyl, whereby the seven latter radicals can be partially or totally halogenated and/or optionally can support one, two or three substitutes, selected among nitro, cyano, OH, C 1 -C 2 -alkoxy, C 1 -C 4 -alkoxycarbonyl, amino, C 1 -C 4 -alkylamino and Di-C 1 -C 4 -alkylamino, Het represents a substituted C- or N-bound, 5-or 6-membered aromatic heterocycle which comprises 1, 2, 3 or 4 heteroatoms as ring members selected among nitrogen, oxygen and sulphur. The invention also relates to the use of 5-hetaryl-4-pyrimidines of formula (I) and there salts for combating plant pathogenic fungi.
Abstract:
The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R represents alkyl, alkoxyalkyl, alkenyl or alkynyl; R represents alkyl, alkoxyalkyl, alkenyl or alkynyl, R and/or R being substituted according to the description. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.
Abstract:
Substituted 6-(2-halogenphenyl)-triazolopyrimidines of formula (I) in which R1 denote alkyl, alkenyl, alkynyl, alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or a 5- or 6-membered saturated, unsaturated, or aromatic heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, wherein R and R radicals may be substituted as defined in the description, R denote hydrogen, or a group mentioned for R ; or R and R together with the interjacent nitrogen atom represent a 5- or 6-membered heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which ring may be substituted as defined in the description; Hal is halogen; L , L independently denote hydrogen, halogen, or alkyl; L is hydrogen, halogen, haloalkyl, or NH2, NHR , or N(Rb)2, wherein Rb is as defined in the description,wherein at least one from L , L , and L is not hydrogen; X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
Abstract translation:取代的式(I)的6-(2-卤代苯基) - 三唑并嘧啶,其中R1表示烷基,烯基,炔基,链二烯基,卤代烷基,卤代烯基,环烷基,苯基,萘基或5-或6-元饱和,不饱和或 芳族杂环,其含有1-4个氮原子或一至三个氮原子和一个硫或氧原子,其中R 1和R 2基团可以如说明书中所定义地被取代,R 2表示氢,或 R 1中提到的基团; 或R 1和R 2连同相邻的氮原子表示含有1-4个氮原子或1-3个氮原子和一个硫或氧原子的5-或6-元杂环,该环可以被取代 如说明书中所定义的; 卤素是卤素; L 1,L 3独立地表示氢,卤素或烷基; L 2是氢,卤素,卤代烷基或NH 2,NHR b或N(R b)2,其中R b如说明书中所定义,其中至少一个L 1,L 2, 而L 3不是氢; X是卤素,氰基,烷基,烷氧基,卤代烷氧基或烯氧基,它们的制备方法,含有它们的组合物和它们用于防治植物病原性真菌的用途。
Abstract:
The invention relates to agrochemical compositions with a fungicidal action, containing compounds of formula (I) as their active agents. The radicals of said formula have the following meanings: R means hydrogen, C1-C6-alkyl, C1-C6-alkylcarbonyl, formyl or C1-C6-halogenalkylcarbonyl; R means halogen, C1-C6-alkylthio, C1-C6-alkoxy, C3-C6-cycloalkyl-C1-C6-alkoxy, C1-C6-alkoxy-C1-C6-alkyl, halogen-C1-C6-alkoxy, C1-C6-alkylsulfonyl, C1-C6-alkylsulfinyl, halogen-C1-C6-alkylsulfonyl, cyano or a radical NR R ; R -R mean hydrogen, halogen, C1-C8-cycloalkyl, C1-C6-alkyl, halogen-C1-C6-alkyl, C1-C6-alkoxy, halogen-C1-C6-alkoxy, C1-C6-alkylsulfonyl, halogen-C1-C6-alkylsulfonyl, formyl, C1-C6-alkylcarbonyl, cyano, C1-C6-alkylthio or phenyl, which can optionally be substituted by halogen atoms, C1-C6-alkyl or halogen-C1-C6-alkyl groups; R means hydrogen, C1-C6-alkyl; and R means C1-C6-alkyl, C1-C8-cycloalkyl or together with R and the nitrogen atom to which they are bonded, a saturated or unsaturated heterocyclic five or six-membered ring which has one or two heteroatoms selected from a group consisting of nitrogen atoms and oxygen atoms. The invention also relates to salts of said compositions which are suitable for agricultural use.
Abstract:
The invention relates to novel cycloalkylalkane carboxylic acid amides of the general formula (I), as well as salts thereof which are suitable for use in agriculture, in which the substituents have the following meanings: A is C3-C6 cycloalkyl which can carry one or more substituents; Alk is straight-chain or branched C1-C6-alkylene; R is C1-C6-alkyl or C2-C6-alkenyl, which can carry one or more substituents; R , R are hydrogen, C1-C6-alkyl or C2-C6-alkenyl, which rests can be partly or fully halogenated; and W is a fused bicyclic ring system with six ring atoms each. The invention also relates to fungicidal agents containing a compound of formula (I) as plant protectant.
Abstract:
Biphenylsulfonamides of the formula (I) and the N-oxides and the agriculturally acceptable salts and the veterinarily acceptable salts of the compounds I, a process for preparing these compounds, compositions comprising them, their use for controlling phytopathogenic harmful fungi and harmful arthropodes, a method for combating arthropodal pests, a method for protecting crops from attack or infestation of arthropodal pests, a method for protecting seed and non-living materials from infestation by arthropodal pests, a method for protecting non-living materials from attack or infestation by arthropodal pests and seed comprising the compounds I.
Abstract:
The invention relates to 2-substituted 7-amino-azolopyrimidine of formula (I), wherein substituents have the following meanings: R 1 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, Cycloalkyl, alkoxy, alkoxyalkyl, benzyloxyalkyl, alkoxyalkenyl or akoxyalkinyl; R 2 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkoxyalkyl and alkylthioalkyl, wherein a carbon chain in R 1 and/or R 2 are substitutable according to a description; R 3 is halogen, Cyano, NR A R B , hydroxy, mercapto, alkyl, halogenalkyl, cycloalkyl, alkoxy, alkylthio, cycloalkoxy, cycloalkylthio, carboxyl, formyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, phenyl, phenoxy, phe- nylthio, benzyloxy, benzylthio, alkyl-S(O) m- ; A N and CR x ; R x is hydrogen or one of above groups for R 3 . A method and intermediate products for producing said compounds, agents containing said compounds and the use thereof for combating plant-pathogen fungi are also disclosed.
Abstract translation:2-取代的式(I)其中取代基具有以下含义的7-氨基azolopyrimidines:R t 1 SUP>为氢,卤素,氰基,烷基,卤代烷基,烯基,炔基,环烷基,烷氧基,烷氧基烷基, benzyloxyalkyl,烷氧基烯基或alkoxyalkynyl; [R 2 SUP>为氢,卤素,氰基,烷基,卤代烷基,烯基,炔基,环烷基,烷氧基,烷氧基烷基和烷硫基烷基,其中在R中的碳链 1 SUP>和/或R 2 SUP>可以根据描述被取代; [R 3 SUP>为卤素,氰基,NR 一 SUP> - [R 乙 SUP>,羟基,巯基,烷基,卤代烷基,环烷基,烷氧基,烷硫基,环烷氧基,环烷硫基, 羧基,甲酰基,烷基羰基,烷氧基羰基,烯氧基羰基,炔氧基羰基,苯基,苯氧基,苯丙氨酸nylthio,苄氧基,苄硫基,烷基-S(O)米 - SUB>; A N和CR X SUP>; ,R 3 SUP>基 X SUP>是氢或其中R 称作; 的方法和中间体制备这些化合物,含有它们和它们在防治植物病原性有害真菌的组合物。
Abstract:
The invention relates to 6-(2,6-dichlorophenyl)-triazolopyrimidines of formula (I) wherein the substituents have the following designations: R and R represent hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group containing O, N or S; R and R can also form, together with the nitrogen atom to which they are bound, a five-membered or six-membered heterocycle or heteroaryl which is bound by N and contains between one and three other heteroatoms from the group containing O, N and S as a cyclic member and is substituted according to the description; and X represents alkyl, cyano, alkoxy, halogenalkoxy, alkenyloxy or halogenalkenyloxy, but does not represent C1-C4 alkyl when R and R together represent piperidin-1-yl or 4-methylpiperidin-1-yl. The invention also relates to a method for producing said compounds, agents containing the same, and the use thereof for controlling plant pathogenic fungi.