Abstract: The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzoazepines of Formula I as selective 5-HT2C receptor agonists for the treatment of 5-HT2C associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety: where: R6 is -C?C-R10, -O-R12, -S-R14, or -NR24R25; and other substituents are as defined in the specification.

Abstract: The present invention relates to heteroaroyl-substituted alanines of the formula I in which the variables A and R1 to R7 are as defined in the description, and to their agriculturally useful salts, to processes and intermediates for their preparation, and to the use of these compounds or of compositions comprising these compounds for controlling unwanted plants.

Abstract: A herbicidal composition comprising a) at least one 3-phenyluracils of formula I wherein the variables R1 to R7 are as defined in the specification; and b) at least one 3-sulfonylisoxazoline of formula II wherein the variables R8 and R9 are as defined in the specification; and c) optionally at least one safener III selected from the group as defined in the specification.

Abstract: The present invention relates to benzoyl-substituted alanines of the formula I in which the variables R1 to R12 are as defined in the description, and to their agriculturally useful salts, to processes and intermediates for their preparation, and to the use of these compounds or of compositions comprising these compounds for controlling unwanted plants.

Abstract: The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines of Formula (I) as selective 5-HT2c receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety, where, R6 is —NR10R11, where R10 is substituted phenylalkyl or substituted pyridylalkyl and other substituents are as defined in the specification.

Abstract: The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines of Formula (I) as selective 5-HT2C receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety: R6 D R?N—R?R* where R6 is —(CrC3)alkyl-S—(C0-C3)alkyl-R10, —(C1-C3)alkyl-NR11R12, —(CrC3)alkyl-O—R13. and other substituents are as defined in the specification.

Abstract: A herbicidal mixture comprising A) exo(+)-1 -methyl-4-(1-methylethyl)-2-[(2-methylphenyl)methoxy]-7-oxabicyclo[2.2.1]heptane (Common Name Cinmethylin) including its respective isomers and B) at least one herbicidal compound of the group of dinitro anilines of formula (I) in which the substituents have the following meanings R1 C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkinyl R2 H, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkinyl R3, R4, R5 the same or different H, halogen, nitro, CN, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkinyl, C1-C10-halogenalkyl, C2-C10-halogenalkenyl, C3-C10-halogenalkinyl, —SOR6, —SO2R6, —OR7, —SR7, —N(R8)2 R6 C1-C10-alkyl, NH2 R7 H, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkinyl, C1-C10-halogenalkyl C3-C10-halogenalkinyl R8 H, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkinyl including their respective isomers as well as their respective environmentally compatible salts.

Abstract: The present invention relates to benzoyl-substituted serineamides of the formula I in which the variables R1 to R11 are as defined in the description, and to their agriculturally useful salts, to processes and intermediates for their preparation, and to the use of these compounds or of compositions comprising these compounds for controlling unwanted plants.

Abstract: The present invention relates to heteroaroyl-substituted serineamides of the formula I in which the variables A and R1 to R6 are as defined in the description, and to their agriculturally useful salts, to processes and intermediates for their preparation, and to the use of these compounds or of the compositions comprising these compounds for controlling unwanted plants.

Abstract: The present invention relates to benzoyl-substituted serineamides of the formula I in which the variables Het and R1 to R10 are as defined in the description, and to their agriculturally useful salts, to processes and intermediates for their preparation, and to the use of these compounds or of the compositions comprising these compounds for controlling unwanted plants.

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: The present invention relates to heteroaroyl-substituted serinamides of the formula I in which the variables A, Het and R1 to R5 are as defined in the description, and to their agriculturally useful salts, to processes and intermediates for their preparation, and to the use of these compounds or of the compositions comprising these compounds for controlling unwanted plants.

Abstract: The present invention relates to benzoyl-substituted phenylalanineamides of the formula I in which the variables R1 to R15 are as defined in the description, and to their agriculturally useful salts, to processes and intermediates for their preparation and to the use of these compounds or of compositions comprising these compounds for controlling unwanted plants.

Abstract: The present invention relates to a process for preparing sulfamoyl halides of primary or secondary amines, comprising the following steps: i) reacting a primary or secondary amine A1 with at least equimolar amounts of SO3 or an SO3 source in the presence of at least equimolar amounts of a tertiary amine A2, based in each case on the amine A1, and ii) reacting the reaction mixture obtained in step i) with at least the amount of a phosphorus halide required by the stoichiometry; The invention further relates to a process for preparing sulfonic diamides, comprising the preparation of sulfamoyl halides by means of carrying out steps i) and ii) and subsequently reacting the sulfamoyl halide obtained with ammonia. The invention further relates to the use of this process for preparing active herbicidal ingredients having a sulfuric diamide structure. The invention further relates to novel sulfamoyl chlorides.

Abstract: Pyrazolylcarbonyl-substituted phenylalanineamides of the formula I in which the variables A and R1 to R10 are as defined in the description, 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 unwanted plants are described.

Abstract: A process is described for preparing 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I, by reacting a phenyl iso(thio)cyanate of the formula II with an enamine of the formula III and, if appropriate, in a further step, the resulting 3-phenyl(thio)uracil or 3-phenyldithiouracil of the formula I where R1=R1a, when R1=hydrogen, is reacted with an aminating agent of the formula IV to give 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I where R1=amino where the variables R1, R1a, R2, R3, R4, X1, X2, X3, Ar, A and L1 are each as defined in claim 1.

Abstract: The present invention relates to benzenesulfonamide derivatives of the formula I in which the variables are as defined below: X1 is hydrogen or halogen; X2 is hydrogen, cyano, CS—NH2, halogen, alkyl or haloalkyl; X3 is hydrogen, cyano, alkyl, alkoxyalkyl, cycloalkyl, alkenyl, alkynyl or phenylalkyl, where the phenyl radical for its part may be substituted; Y is a group —C(A)B, SO2 or SO2NR2; A is oxygen or sulfur; B is oxygen, sulfur, NR2 or a bond; R1 is hydrogen, halogen, hydroxy, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, cycloalkenyl, alkynyl, alkoxy, cycloalkyloxy, alkenyloxy, alkynyloxy, aryl, aryloxy, arylalkyl, where the 13 last mentioned radicals for their part may be substituted; unsubstituted or substituted four- to six-membered heterocyclyl; unsubstituted or substituted four- to six-membered heterocyclyl-C1-C4-alkyl; unsubstituted or substituted five- or six-membered heteroaryl having one to four nitrogen atoms or having one to three nitrogen atoms and one oxygen or one sulfur atom

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: A process for preparing phenyl iso(thio)cyanates of the formula I in which a compound of the formula II or its HCl adduct is reacted with a phosgenating agent where W is oxygen or sulfur and Ar and A are as defined in claim 1 is described. Moreover, the invention relates to the use of the phenyl iso(thio)cyanates for preparing crop protection agents.

Abstract: The present invention provides serotonergic benzofurylpiperazines of Formula I: where: A is a piperazine of formula: and R, R1, R2, R3, R4, R5, R5?, R6, R6?, R7, R7?, R8, and R8? are as described in the specification.