Abstract:
Compounds have the formula (I), in which Ar?1 and Ar2¿ stand for aryl or heteroaryl, which may be substituted, and R stands for a possibly substituted aliphatic or alicyclic residue. Also disclosed are a process for preparing the same, an agent containing the same and its use for controlling animal pests.
Abstract:
PCT No. PCT/EP93/03128 Sec. 371 Date Jul. 3, 1995 Sec. 102(e) Date Jul. 3, 1995 PCT Filed Nov. 9, 1993 PCT Pub. No. WO94/10846 PCT Pub. Date May 26, 1994The present invention relates to insecticidal and acaricidal compositions which comprise an effective content of endosulfan (A) (A) in combination with the entomopathogenic fungus Beauveria bassiana (B).
Abstract:
The invention relates to compounds of the formula defined in the description, X is NH or oxygen and E is a bond or a 1- to 4-membered carbon chain, to a process for their preparation, to agents containing them, and to their use in the control of pests and as fungicides.
Abstract:
The invention relates to substituted 4-alkoxypyrimidines of the formula in which R denotes hydrogen, halogen, alkyl or cycloalkyl, R denotes hydrogen, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted alkylthio, alkylamino or dialkylamino, R denotes hydrogen, alkyl, alkoxy, haloalkoxy, halogen, alkylthio, amino, alkylamino or dialkylamino and R denotes hydrogen, alkyl, cycloalkyl or haloalkyl, where R and R together with the C atoms carrying them can also form a ring and Q has the meanings defined in the description. The invention furthermore relates to a process for their preparation, agents containing them and their use as pesticides.
Abstract:
Compounds of the formula (I) and their stereoisomers (I) wherein A, B, C' and D independently of one another denote CH or N, in which at least one of the symbols A, B, C' or D must correspond to a nitrogen atom, X denotes CH2 or oxygen, R1 denotes a radical bonded to a carbon atom from the series comprising H, trialkylsilyl, halogen, nitro, cyano, alkenyl, alkynyl, amino, cycloalkyl, phenyl, phenxy, alkoxy, alkenyloxy, alkynyloxy, hydroxycarbonyl, alkylthio, cycloalkyloxy, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, halogenoalkyl, alkoxyalkyl, halogenoalkoxy, halogenoalkylthio, halogenoalkoxyalkyl, alkylthioalkyl, alkoxyalkoxy, halogenoalkoxyalkoxy, alkenyloxyalkoxy, halogenoalkenyloxy, alkoxyalkylthio, alkylthioalkoxy, alkylthioalkylthio, halogenoalkoxycarbonyl, halogenoalkenyloxycarbonyl or dialkylamino or two radicals R1 when they are positioned ortho to one another together denote a methylenedioxy, ethylenedioxy or alkylene radical, R2 and R3 independently of one another denote alkyl, alkenyl or phenyl, or R2 and R3 denote an alkylene chain which-together with the quaternary carbon atom-forms an unsubstituted or fluorinesubstituted ring having three to six ring members, R4 denotes -H, F, -CN, -CCl3, -C 3BOND CH, (C1-C4)alkyl, -C-NH2, S R5 denotes pyridyl, furyl or thienyl which can all be substituted, phthalimidyl, dialkylmaleimidyl, thiophthalimidyl, dihydrophthalimidyl, tetrahydrophthalimidyl or substituted phenyl, or R4 and R5-together with the carbon atom bridging them-denote an optionally substituted indanyl, cyclopentenoyl or cyclopentenyl radical and n denotes 0, 1 or 2, possess advantageous properties for combating pests, in particular insects and acarids. Furthermore, processes for the preparation of compounds of the formula I are described.
Abstract:
The compounds of the formulae I and II, their stereoisomers and the mixtures of these in which R represents pyridyl, pyrimidyl, thienyl, thiazolyl, furanyl, pyrazolyl, 1,3-oxazolyl or imidazolyl, each of which can be substituted, R represents H, (C1-C4)alkyl, (C1-C4)haloalkyl, (C1-C4)alkoxy, (C3-C6)cycloalkyl, -CH=CH2 or -C IDENTICAL CH, R represents H or (C1-C4)alkyl, R represents H, (C1-C4)alkyl, -CN or -C IDENTICAL CH, A represents CH2, O or S, B represents CH, N or C(CH3), R represents H or halogen and R represents phenyl, phenoxy or benzyl, each of which can be monosubstituted to pentasubstituted by halogen or (C1-C3)haloalkyl, have advantageous insecticidal or acaricidal properties.
Abstract:
of the disclosure Heteroaryl-aryl-butene and -butane derivatives, process for their preparation, agents containing them, and their use as pesticids Compounds of the fonmulae I and II, the stereoisomers thereof, and the mixtures of the latter (I) (II) where R1 is pyridyl, pyrimidyl, thienyl, thiazolyl, furanyl, pyrazolyl, 1,3-oxazolyl or imidazolyl, all of which can be substituted, R2 is H, (C1-C4)alkyl, (C1-C4)haloalkyl, (C1-C4)alkoxy (C3-C6)cycloalkyl, -CH=CH2 or -C=CH, R3 is H or (C1-C4)alkyl, R4 is H, (C1-C4)alkyl, -CN or -C=CH, A is CH2, 0 or S, B is CH, N or C(CH3), R5 is H or halogen and R6 is phenyl, phenoxy or benzyl, all of which can be monosubstituted to pentasubstituted by halogen or (C1-C3)haloalkyl, have advantageous insecticidal or acaricidal properties.
Abstract:
Compounds of the formula I, their optical isomers and mixtures thereof … … in which… M represents C or Si,… R represents unsubstituted or substituted pyridyl, unsubstituted or substituted pyrimidyl, and - when M = C - unsubstituted or substituted pyridazinyl, unsubstituted or substituted pyrazinyl, unsubstituted or substituted 1,2,4-triazinyl, unsubstituted or substituted 1,2,4,5-tetrazinyl,… R , R independently of one another represent alkyl, alkenyl, haloalkyl, phenyl, or R and R represent an alkylene chain which - together with the quaternary central atom (M)- forms an unsubstituted or fluorine-substituted ring having four to six ring members (when M = Si) or having three to six ring members (when M = C),… R represents H, F, -CN, -CCl3, -C IDENTICAL CH, (C1-C4)alkyl, - @ -NH2,… R represents pyridyl, furyl, thienyl, all of which can be substituted, phthalimidyl, dialkylmaleimidyl, thiophthalimidyl, dihydrophthalimidyl, tetrahydrophthalimidyl, substituted phenyl,… or R and R - together with the carbon atom linking them - form an optionally substituted indanyl, cyclopentenoyl or cyclopentenyl radical,… and their salts and quaternisation products have advantageous insecticidal, acaricidal or nematocidal properties.