Abstract: A wood preservative which contains a dimethylalkylamine, an aliphatic C8-C20-dicarboxylic acid and a triazole compound.

Abstract: Substituted cyclohexene-1,2-dicarboxylic acid derivatives I (R1 and R2 are each H, unsubstituted or substituted C1-C6-alkyl, C3-C6-alkenyl or C3-C6-alkynyl, C3-C8-cycloalkyl, unsubstituted or substituted phenyl or heterocyclyl and, if R1 is H or C1-C6-alkyl, R2 is additionally OH, C1-C6-alkoxy, C3-C6-alkenyloxy, C3-C6-alkynyloxy, C3-C6-cycloalkoxy, C5-C7-cycloalkenyloxy, C1-C6-haloalkoxy, C3-C6-haloalkenyloxy, C3-C7-cycloalkyl-C1-C6-alkoxy, C1-C6-alkyl-carbonyloxy, C1-C6-cyanoalkoxy, hydroxy-C1-C6-alkoxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkoxycarbonyl-C1-C6-alkoxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkylamino-C1-C6-alkoxy, C1-C6-dialkylamino-C1-C6-alkoxy, unsubstituted or substituted phenyl-C1-C6-alkoxy, phenyl-C3-C6-alkenyloxy or phenyl-C3-C7-alkynyloxy or unsubstituted or substituted amino, or R1 and R2, together with the nitrogen atom to which they are bonded, form an unsubstituted or substituted 3-membered to 8-membered heterocyclic structure, R3 is H or C1-C6-alkyl, R4 is H or halogen

Abstract: Thiazolimine derivatives of the formula I ##STR1## where: X and Y independently of one another are each hydrogen, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl;Z is hydrogen; C.sub.l -C.sub.8 -alkyl, C.sub.2 -C.sub.8 -alkenyl, C.sub.2 -C.sub.8 -alkynyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.8 -alkylthio, it being possible for these groups to be substituted by one to five halogen or C.sub.1 -C.sub.4 -alkoxy; aryl, hetaryl, benzyl, it being possible for these groups to be substituted by C.sub.l -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.l -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, halogen, nitro or cyano; or one of the groups below: ##STR2## R.sup.1 and R.sup.2 are each hydrogen, halogen; C.sub.1 -C.sub.4 -alkyl, C.sub.2 -C.sub.4 -alkenyl, C.sub.2 -C.sub.4 -alkynyl, it being possible for these groups to be substituted by one to five halogens or by C.sub.1 -C.sub.4 -alkoxy;n is 1 or 2;m is 0, 1 or 2R.sup.3 -R.sup.

Abstract: Heterocyclic substituted benzoyl derivatives of the formula ##STR1## where Z is a 5-membered or 6-membered heterocyclic, saturated or unsaturated radical containing one to three hetero atoms selected from the group consisting of oxygen, sulfur and nitrogen, useful as intermediates for herbicidal compounds.

Abstract: 4-(3-Alkenylbenzoyl)pyrazoles of the formula I ##STR1## and agriculturally useful salts thereof; processes for preparing the compounds of the formula I; compositions comprising them; and the use of these derivatives or of compositions comprising them for controlling undesirable plants.

Abstract: 4-Benzoylpyrazoles of the formula I where:A is a group of the formula IIIa, IIIb or IV ##STR1## Q is a pyrazole of the formula II, ##STR2## useful as herbicides.

Abstract: 2-Benzoylcyclohexane-1,3-diones of the formula I: ##STR1## where: R.sup.1 and R.sup.2 are each hydrogen, mercapto, nitro, halogen, cyano, thiocyanato, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkynyl, --OR.sup.10, --OCOR.sup.10, --OSO.sub.2 R.sup.10, --S(O).sub.n R.sup.10, --SO.sub.2 OR.sup.10, --SO.sub.2 NR.sup.3 R.sup.10, --NR.sup.10 SO.sub.2 R.sup.10 or --NR.sup.10 COR;Q is a cyclohexane-1,3-dione ring with or without substitution, which is attached in position 2;A is a group of the formula IIa, IIb or III: ##STR2## where the substituents are as defined in claim 1, and agriculturally useful salts thereof are described.

Abstract: Sulfur-containing 2-chloro-3-(4,5-dihydro-3-isoxazolyl)-benzoic acids of the formula I in which the substituents have the meanings given in the description are prepared as described.

Abstract: 5-(Dioxabicyclohept-6-yl)cyclohexenone oxime ethers of the formula I ##STR1## where: R.sup.1 is hydrogen, the equivalent of an agriculturally useful cation, C.sub.1 -C.sub.10 -alkylcarbonyl, C.sub.1 -C.sub.10 -alkylsulfonyl, C.sub.1 -C.sub.10 -alkylphosphonyl, benzoyl, benzenesulfonyl or benzenephosphonyl;R.sup.2 is C.sub.1 -C.sub.6 -alkyl;R.sup.3 is in each case, independently of the others, hydrogen or C.sub.1 -C.sub.4 -alkyl;Z is a C.sub.1 -C.sub.6 -alkylene, C.sub.3 -C.sub.6 -alkenylene or C.sub.3 -C.sub.6 -alkynylene chain which may carry an exo-methylene substituent (.dbd.CH.sub.2) and/or in each case one to three additional substituents selected from the group consisting of C.sub.1 -C.sub.3 -alkyl substituents and halogen atoms,is a C.sub.3 --C.sub.6 -alkylene or C.sub.4 --C.sub.6 -alkenylene chain which may carry one to three C.sub.1 -C.sub.3 -alkyl substituents and which contains, in addition to methylene or methine units, one of the following bridge members: oxygen, sulfur, --SO--, --SO.sub.

Abstract: 4-Benzoylisothiazoles of the formula 1 ##STR1## wherein x is oxygen or sulfur;R.sup.1 is hydrogen, alkyl, alkenyl, alkynyl; or is optionally substituted alkoxycarbonyl, aryl, heterocyclyl or hetaryl;R.sup.2 is hydrogen, halogen, cyano, nitro, alkylsulfonyl or alkoxycarbonyl; or is optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, aryloxy, arylthio, alkylamino, arylamino, hetaryl or heterocyclyl;R.sup.3 is optionally substituted alkyl, cycloalkyl or aryl, or their salts, their manufacture and herbicidal compositions containing them.

Abstract: Saccharin-5-carbonylcyclohexane-1,3,5-trione derivatives of the formula I ##STR1## where: L is C.sub.1 -C.sub.3 -alkyl or C.sub.1 -C.sub.3 -alkoxy;Z is C.sub.1 -C.sub.4 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.5 -alkynyl, benzyl or phenyl, the phenyl rings in each case being unsubstituted or mono- or polysubstituted by C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.3 -alkoxy or halogen;M is hydrogen, C.sub.1 -C.sub.3 -alkyl, C.sub.1 -C.sub.3 -alkoxy, fluorine, chlorine, cyano, nitro or trifluoromethyl;R.sup.1, R.sup.2, R.sup.3, R.sup.4 are each C.sub.1 -C.sub.4 -alkyl;and agriculturally useful salts of compound I.

Abstract: Benzoyl derivatives of the formula I ##STR1## where the substituents L, M, X, Y and n have the meaning given in claim 1 andQ for [sic] a cyclohexane-1,3-dione ring, which is linked in the 2-position, of the formula II, ##STR2## where R.sup.15, R.sup.16, R.sup.18 and R.sup.20 are hydrogen or C.sub.1 -C.sub.4 -alkyl,R.sup.19 is hydrogen, C.sub.1 -C.sub.4 -alkyl or a group --COOR.sup.14,R.sup.17 is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.3 -C.sub.4 -cycloalkyl, it being possible for these groups, if desired, to carry one to three of the following substituents: halogen, C.sub.1 -C.sub.4 -alkylthio or C.sub.1 -C.sub.4 -alkoxy,orR.sup.17 is tetrahydropyran-3-yl, tetrahydropyran-4-yl or tetrahydrothiopyran-3-ylorR.sup.17 and R.sup.20 together form a bond or a three to six-membered carbocyclic ring,where in the case where Y=C.dbd.O, X is not equal to NR.sup.23,and agriculturally utilizable salts, a process for their preparation and their use as herbicides are described.

Abstract: 4-Benzoylisothiazoles of the general formula 1 ##STR1## where the substituents have the following meanings: X is oxygen or sulfur;R.sup.3 is a radical of the general formula 2 ##STR2## where Z and the substituents R.sup.1, R.sup.2, R.sup.4, R.sup.5, R.sup.6 and R.sup.7 have the meanings given in claim 1,salts of the 4-benzoylisothiazoles of the general formula 1 which are conventionally used in agriculture, their preparation, and their use as herbicides.

Abstract: 2- Aroylcyclohexanediones I ##STR1## where X, Y=O or S;Ar=phenyl or heteroaryl in each case having 1-4 substituents: halogen, cyano, nitro, --N.dbd.N--Ph, C.sub.1 -C.sub.4 -alkoxycarbonyl, --N(R.sup.9)--COR.sup.10, --N(R.sup.9)--SO.sub.2 --R.sup.11, --SO.sub.2 --N(R.sup.9)R.sup.10, --S(O).sub.m --R.sup.8 or opt. subst. C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl or C.sub.1 -C.sub.4 -haloalkoxy;two adjacent C atoms of the phenyl or heteroaryl ring can also be bridged by means of a chain --C(R.sup.12).dbd.C(R.sup.13)--C(R.sup.14).dbd.C(R.sup.15)--, --Z.sup.1 --C(R.sup.12).dbd.N--, --Z.sup.1 --N.dbd.C(R.sup.12)--, --Z.sub.1 --C(R.sup.12).dbd.C(R.sup.13)--, --Z.sup.1 --C(R.sup.12).dbd.C(R.sup.13)--C(R.sup.14,R.sup.15)--, --Z.sup.1 --C (R.sup.12,R.sup.13)--C(R.sup.14,R.sup.15)--, --Z.sup.1 --C(R.sup.12,R.sup.13)--C(R.sup.14 R.sup.15)--Z.sup.2 --, --C(R.sup.12,R.sup.13)--Z.sup.1 --C(R.sup.14,R.sup.15)--C(R.sup.16,R.sup.17)--, --Z.sup.1 --N(R.sup.20)--Z.sup.2 --, --Z.sup.1 --Z.sup.

Abstract: There are described N-aminopyridone derivatives of the formula I: ##STR1## where the substituents R.sup.1 to R.sup.12 have the meanings given in claim 1, a process for their preparation, and their use for controlling undesirable vegetation.

Abstract: The invention relates to 4-benzoylpyrazoles of the formula I and their agriculturally useful salts thereof, processes and intermediates; compositions thereof; and use thereof for controlling undesireable plants.

Abstract: Hetaroyl derivatives of the formula I ##STR1## where the substituents have the following meanings: L and M hydrogen, C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkynyl, C.sub.1 -C.sub.4 -alkoxy, it being possible for these groups to be unsubstituted or substituted by one to five halogen atoms or C.sub.1 -C.sub.4 -alkoxy; halogen, cyano, nitro;X oxygen or sulfur which can be substituted by one or two oxygens;n zero, one, two;Q,R.sup.1,R.sup.2,R.sup.3 and R.sup.4 have the meanings given in claim 1,processes for preparing the hetaroyl derivatives, compositions which contain them and the use of these derivatives or compositions containing them for controlling weeds are described.

Abstract: Benzoyl derivatives of the formula I ##STR1## where Z is a 5-membered or 6-membered heterocyclic, saturated or unsaturated radical containing one to three hetero atoms selected from the group consisting of oxygen, sulfur and nitrogen,Q is a cyclohexane-1, 3-dione ring bonded in the 2-position and of the formula II, ##STR2## or conventional agricultural salts of the compounds I.

Abstract: Quinoline-3-carboxamides I ##STR1## where R.sup.1 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, and the organic radicals may be substituted or unsubstituted;R.sup.2 is hydrogen, hydroxyl, alkoxy, alkenyloxy, dialkylamino, alkyl, alkenyl, alkynyl, cycloalkyl, and the organic radicals may be substituted or unsubstituted;orR.sup.1, R.sup.2 together denote an alkylene chain of 4 to 7 members and which may be interrupted by oxygen, sulfur or N-methyl;R.sup.3 -R.sup.6 are hydrogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkylthio, haloalkylthio, halogen, cyano or nitro;X is oxygen or sulfur;with the proviso that R.sup.2 is not hydrogen, C.sub.1 -C.sub.3 -alkyl, n-butyl, 3-methylbutyl, cyclohexyl, hexyl, heptyl, octyl, 2-chlorobenzyl, 3-(dimethylamino)propyl, 3-(diethylamino)propyl, 2-morpholinoethyl or 2-(3,4-dimethoxyphenyl)ethyl when R.sup.1 and R.sup.3 to R.sup.6 are hydrogen and X is oxygen, and that R.sup.2 is not benzyl when R.sup.1 is methyl, R.sup.3 to R.sup.6 are hydrogen and X is oxygen, and that R.

Abstract: 4-Benzoylisothiazoles of the general formula 1 ##STR1## where the substituents have the following meanings: X is oxygen or sulfur;R.sup.3 is a radical of the general formula 2a-d ##STR2## where n, A, B and the substituents R.sup.4, R.sup.5 and R.sup.6 have the meanings given in claim 1,salts of the 4-benzoylisothiazoles of the general formula 1 which are conventionally used in agriculture, processes for their preparation, and their use as herbicides.