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 present invention relates to compounds of the general formula (I) and to the salts thereof, wherein the substituents and the n index have the following values: Q represents -C(=CHCH3)-COOCH3, -C(=CHOCH3)-COOCH3, -C(=NOCH3)-COOCH3 or -C(=NOCH3)-CONH(CH3); R represents hydrogen, halogen, C1-C4 alkyl, C1-C2 halogenalkyl, C1-C4 alkoxy or C1-C2 halogenalkoxy; R represents halogen, C1-C4 alkyl, C1-C2 halogenalkyl or C1-C4 alkoxy; n is 0, 1 or 2, wherein the R substituents can be different when n = 2; and R represents phenyl, pyridyle or pyrimidyle. This invention also relates to agents containing these compounds as well as to the use of said compounds (I) and agents against noxious fungi and animal parasites.
Abstract translation:通式(I)和它们的盐,其中取代基和指数n具有以下含义的化合物:Q是-C(= CHCH 3)-COOCH 3,-C(= CHOCH 3)-COOCH 3,C(= NOCH 3) - COOCH 3或-C(= NOCH 3)-CONH(CH 3); R 1是氢,卤素,C 1 -C 4烷基,C 1 -C 2卤代烷基,C 1 -C 4烷氧基或C 1 -C 2卤代烷氧基; R 2是卤素,C 1 -C 4烷基,C 1 -C 2卤代烷基,C 1 -C 4烷氧基; n是0,1或2,其中当n = 2时取代基R 2可以不同; R 3苯基,吡啶基或嘧啶基,含有它们的试剂以及化合物(I)和防治有害真菌和动物害虫的试剂的用途。
Abstract:
Настоящееизобретениеотноситсяк замещенным 5-фенилпиримидинамформулы I, которыенесутрадикал X в 4-ойпозициипиримидиновогокольца, радикал Y в 6-ойпозициипиримидиновогокольца, где X означаетгруппуформулы NRR, вкоторой Rозначает C-C-алкил, C-C-алкенил, C-C-галоалкил, C-C-циклоалкил, которыемогутбытьзамещены C-C-алкилом, Rозначаетводород, C-C-алкилили C-C-алкенил, радикал Y выбираетсяизгруппы, состоящейизгалогенаи С-С-алкилаи фармацевтическиприемлемымсолямзамещенного 5-фенилпиримидина I дляпримененияв терапииилилечениираковыхзаболеваний.
Abstract:
Popisují se fungicidní smesi obsahující jako aktivní složky a) slouceninu vzorce I, její N-oxid nebo jednu z jejích solí, kde: R.sup.1.n., R.sup.2.n., R.sup.3.n., R.sup.4.n. jsou nezávisle na sobe: vodík, hydroxyl, nitro, halogen, C.sub.1-4.n.alkyl, C.sub.1-4.n.halogenalkyl, C.sub.1-4.n.alkoxy, C.sub.1-4.n.halogenalkoxy, C.sub.1-4.n.alkylthio, C.sub.1-4.n.halogenalkylthio; R.sup.5.n., R.sup.6.n., R.sup.7.n. jsou nezávisle na sobe: vodík, hydroxyl, kyano, nitro, halogen, C.sub.1-7.n.alkyl, C.sub.1-7.n.halogenalkyl, C.sub.1-7.n.alkoxy, C.sub.1-7.n.halogenalkoxy, C.sub.1-7.n.alkylthio, C.sub.1-7.n.halogenalkylthio, C.sub.1-7.n.hydroxyalkyl, C.sub.2-4.n.acyl, aryl, aryloxy, kde skupiny obsahující jako soucást aryl mohou být jednou až trikrát substituovány následujícími skupinami: kyano, nitro, halogen, C.sub.1-4.n.alkyl, C.sub.1-4.n.halogenalkyl, C.sub.1-4.n.alkoxy, C.sub.1-4.n.halogenalkoxy, C.sub.1-4.n.alkylthio a C.sub.1-4.n.halogenalkylthio, a b) karbamáty vzorce II, kde T je CH nebo dusík, n je 0, 1 nebo 2 a R je halogen, C.sub.1-4.n.alkyl, nebo C.sub.1-4.n.halogenalkyl, kdy R mohou být ruzné, pokud n je 2, v synergicky úcinném množství.
Abstract:
Oxazin(ethi)one compounds of the formula I: in which the variables Z, R 1 , R 2 , R 3 and n are as defined in claim 1 and A is a 5- or 6-membered carbocycle or a 5- or 6-membered heterocycle having 1, 2 or 3 heteroatoms selected from the group consisting of N, O and S, each of which cycles is attached via two carbon atoms to the oxazin(ethi)one ring, and the agriculturally useful salts of the oxazin(ethi)one compounds I are described. Moreover, the invention describes the use of compounds I and their salts for controlling phytopathogenic fungi, compositions which comprise the compounds I and/or their salts in a fungicidally effective amount and a method for controlling phytopathogenic fungi which comprises treating the fungi or the materials, plants, seeds or the soil threatened by fungal attack with a fungicidally effective amount of at least one compound of the formula I as claimed in claim 1 and/or a salt of I.
Abstract:
Disclosed is a fungicidal mixture, comprising the triazolopyrimidine derivative of formula I and fenpropimorph of formula II in a synergistically effective amount. Also disclosed is a method for controlling harmful fungi which are rice pathogens, such as Corticium sasakii, which comprises treating the fungi, their habitat or the plants, the soil or the seeds to be protected against fungal attack with an effective amount of the above mixture.
Abstract:
Disclosed is a fungicidal mixture comprising 1) the triazolopyrimidine derivative of the formula I and 2) dodine of the formula II in a synergistically effective amount. Also disclosed is a method for controlling harmful fungi which are rice pathogens, which comprises treating the fungi, their habitat or the seed, the soil or the plants to be protected against fungal attack with an effective amount of the compound I and the compound II.