Abstract: A herbicidal mixture, comprising A) picolinafen (I) ?or an agriculturally useful salt thereof, and B) at least one further herbicide selected from the group of the phthalamates (B1), semicarbazones (B2), chloracetanilides (B3), carbamates (B4), pyridazines (B5), dinitrophenols (B6), dipyridylenes (B7), benzothiadiazoles (B8), uracils (B9), pyridazinones (B10), phenylcarbamates (B11), benzoic acids (B12), quinolinecarboxylic acids (B13), nitriles (B14), benzamides (B15) and amides (B16).

Abstract: A synergistic herbicidal mixture comprising A) picolinafen; or one of its environmentally compatible salts; and B) a synergistically effective amount of at least a triazolopyrimidine herbicide selected from the triazolopyrimidine sulfonanilides and penoxsulam; or one of its environmentally compatible salts or esters; and, if desired, C) at least a safener. Compositions comprising these mixtures, processes for the preparation of these compositions and their use for controlling undesired plants.

Abstract: A synergistic herbicidal mixture comprising: A) [N-(5,7-Dimethoxy[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)]-3-pyridinesulfonamnid (I) or one of its environmentally compatible salts; B) and at least one herbicidal compound from the group of alloxydim, clethodim, cloproxydim, cycloxydim, butroxydim, clefoxydim, tepraloxydim, cyhalofop-butyl, fenthiapropethyl, fluazifop-P-butyl, isoxapyrifop, propaquizafop, quizalofop-ethyl, quizalofop-P-ethyl quizalofop-tefuryl, flamprop-methyl, flamprop-isopropyl, imazapyr, imazapic, pyrithiobac-acid, pyrithiobac-sodium, bispyribac-sodium, KIH-6127, pyribenzoxym, metosulam, azimsulfuron, bensulfuron-methyl, chlorsulfuron, cinosulfuron, cyclosulfamuron, ethoxysulfuron, flazasulfuron, halosulfuron-methyl, imazosulfuron, primisulfuron-methyl, pyrazosulffuron-ethyl, rirmsulfuron, sulfometuron-methyl, triflusulfuron-methyl, mesosulfuron, iodosulfuron, allidochlor (CDAA), benzoylprop-ethyl, bromobutide, chlorthiamid, diphenamid, etobenzanid (benzchlomet),

Abstract: The invention relates to 1-phenylpyrrolidin-2-one-3-carboxamides of the formula I where the variables R1, R2, R3, X, Y, A, n, Ra, Rb, Rc, Rd and Re are as defined in claim 1 and to their agriculturally useful salts. Moreover, the invention relates to the use of compounds I and/or their salts as herbicides; crop protection compositions comprising at least one 1-phenylpyrrolidin-2-one-3-carboxamide of the formula I and/or at least one agriculturally useful salt of I as active substances; and also a method for controlling unwanted vegetation, which comprises allowing a herbicidally effective amount of at least one 1-phenylpyrrolidin-2-one-3-carboxamide of the formula I or an agriculturally useful salt of I to act on plants, their habitat or on seed.

Abstract: Disclosed are 3-heterocyclyl substituted benzoic acid derivatives of general formula (I), in which the variables R1 to R8 and X have the meanings indicated in claim 1, and the use thereof as herbicides or for desiccating/defoliating plants.

Abstract: Phenylalanine derivatives of the formula I where the radicals are as defined in the description, and the use of these compounds as herbicides and/or for regulating plant growth is described.

Abstract: A method for increasing the resistance of plants to the phytotoxicity of agrochemicals comprises treating the plants, the soil or seeds with an effective amount of a compound of the formula I in which X is halogen, alkyl or trifluoromethyl; m is 0 or 1; Q is C(?CH—CH3)—COOCH3, C(?CH—OCH3)—COOCH3, C(?N—OCH3)—CONHCH3, C(?N—OCH3)—COOCH3, N(—OCH3)—COOCH3 or a group Q1, where # indicates the bond to the phenyl ring; A is —O—B, —CH2O—B, —OCH2—B, —CH?CH—B, —C—C—B, —CH2O—N?C(R1)—B or —CH2O—N?C(R1)—C(R2)?N—OR3, where B is phenyl, naphthyl, 5-membered or 6-membered hetaryl or 5-membered or 6-membered heterocyclyl, the ring systems being unsubstituted or substituted as specified in the description; R1 is hydrogen, cyano, alkyl, haloalkyl, cycloalkyl or alkoxy; R2 is phenyl, phenylcarbonyl, phenylsulfonyl, 5- or 6-membered hetaryl, 5- or 6-membered hetarylcarbonyl or 5- or 6-membered hetarylsulfonyl, the ring systems being unsubstituted or substituted as specified in the description, alkyl, cycloalkyl, alkenyl

Abstract: 3-Heteroaryl-substituted isoxazolines of the formula I where: X is substituted 5-membered heteroaryl having one to four nitrogen atoms or one to three nitrogen atoms and one oxygen or sulfur atom or one oxygen or sulfur atom; or substituted 6-membered heteroaryl having one to four nitrogen atoms; where the abovementioned 5-membered heteroaryl is not pyrazolyl or thienyl; R1-R7 are hydrogen, alkyl or haloalkyl; Y is unsubstituted or substituted aryl, or benzo[1,4]dioxonyl, benzo[1,3]dioxolanyl, 2,3-dihydrobenzofuranyl or benzimidazole; or unsubstituted or substituted 5- to 6-membered heteroaryl; and their agriculturally useful salts, processes and intermediates for their preparation, and the use of these compounds or of the compositions comprising these compounds for controlling unwanted plants are described.

Abstract: Cyclohexenone derivatives of benzazolones of the formula I where the variables R1, R2, R3, A and Hex are as defined in claim 1, and their salts, and their use for controlling harmful plants, are described.

Abstract: The invention relates to a method of preparing 1-alkyl-3-aryl-5-difluoromethoxy-1H-pyrazoles of the formula (I), wherein aryl represents a mono- or polysubstituted phenyl ring, and R1 represents C1-C4 alkyl. The inventive method is characterized by reacting, in a first reaction step, a ?-ketoester of the general formula (II) with hydrazine and by successively reacting the reaction product obtained with chlorodifluoromethane and a compound R1-L, wherein R1 has the meanings indicated above and L represents the leaving group of a nucleophilic displacement reaction.

Abstract: A process for preparing 7-(pyrazol-3-yl)benzoxazoles of the formula I in which the variables R1-R6 are as defined in claim 1, which process is characterized in that a 2-halo-3-(pyrazol-3-yl)anilide of the formula II, in which X is bromine or iodine is reacted with a base in the presence of a transition metal compound of subgroup VIIa, VIIIa or Ib of the Periodic Table of the Elements, is disclosed.

Abstract: 2,?-Diaminocarboxylic acid compounds of formula (I), where X, X1, Ar?, Ar2 and Y are as defined in claim 1, and their use as herbicides, are described.

Abstract: Herbicidally active compositions comprising: A) at least one 7-pyrazolylbenzoxazole compound of the formula (I) in which the variables R1-R5 are as defined in the patent claims and/or at least one of its agriculaturally acceptable salts; and at least one further active compound selected from herbicidally active compounds and safeners.

Abstract: ?-Cyanoacrylates of the formula I where: R1 is ORa wherein Ra is hydrogen, substituted alkyl, branched alkyl, branched alkenyl, cycloloalkyl, heterocyclyl, aryl, phenylalkyl or alkylimino; is NRbRc wherein Rb is hydrogen, alkyl which may be substituted, alkenyl, alkynyl; Rc is hydrogen, alkyl which may be substituted alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, phenylalkyl or alkylimino; or Rb and Rc form an alkandiyl-chain which may be substituted; or is SRd wherein Rd is hydrogen, alkyl which may be substituted, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, phenylalkyl or alkylimino; R2 is alkyl which may be substituted; is alkenyl or alkynyl; R3 is alkyl may be substituted; is alkenyl or alkynyl; R4 is hydrogen, halogen, cyano or alkyl; and their agriculturally useful salts, processes and intermediates for their preparation; and the use of these compounds or of compositions comprising these compounds for controlling undesirable plants are described.

Abstract: The invention relates to a solid crop protection formulation comprising

Abstract: The invention relates to a solid crop protection formulation comprising

Abstract: Herbidically active compositions, comprising: A) at least one phenyluracil compound of the formula (I); in which the variables R1-R7 are as defined in the claims, and/or at least one of its agriculturally acceptable salts; and at least one further active compound, selected from B) herbicides of classes b1) to b15): b1) lipid biosynthesis inhibitors; b2:) acetolactate synthase inhibitors (ALS inhibitors:); b3:) photosynthesis inhibitors; b4) protoporphyrinogen-IX oxidase inhibitors; b5) bleacher herbicides; b6) enolpyruvyl shikimate 3-phosphate synthase inhibitors (EPSP inhibitors); b7) glutamine synthetase inhibitors; b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors); b9) mitose inhibitors; b10) inhibitors of the synthesis of very long chain fatty acids (VLCFA inhibitors); b11) cellulose biosynthesis inhibitors; b12) decoupler herbicides; b13) auxin herbicides; b14) auxin transport inhibitors: b15) other herbicides selected from the group consisting of benzoylprop, flamprop, flamprop-M, bromobutide

Abstract: Benzoylcyclohexenone derivatives of the formula I 1

Abstract: Pyrazolyl-substituted thienyloxypyridines of the formula I 1

Abstract: 4-Alkyl-substituted thienyloxypyridines of the formula I 1