Abstract: This invention relates to novel triazolopyrimidines of the formula in which R1, R2, R3, R4and X have the meanings given in the disclosure, to a plurality of processes for preparing these novel substances, and to their use for controlling unwanted microorganisms. This invention further relates to novel intermediates of the formulae and processes for their preparation and additionally relates to novel amines and carbamates of the formulae given in the disclosure and processes for their preparation.

Abstract: The present invention relates to active compound combinations of a fluorobenzo-thiazole of the formula (I) and at least one of the compounds listed herein. The active compound combinations of the present invention are useful as fungicides.

Abstract: The present invention relates to fungicidally active compound combinations of a fluorobenzothiazole derivative of the formula (I) and at least one of the compounds listed in the disclosure.

Abstract: This invention relates to novel pyrazolopyrimidines of the formula in which R1, R2, R3, X1 and X2 are as defined in the disclosure, to a process for preparing these substances and to their use for controlling harmful organisms. This invention further relates to novel intermediates of the formulae and to processes for their preparation.

Abstract: Novel triazolopyrimidines of the formula in which G, R and X are as defined in the description, a process for preparing these substances and their use for controlling unwanted microorganisms.

Abstract: Novel triazolopyrimidines of the formula in which R1 represents amino, represents in each case optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, alkylamino, dialkylamino, alkenylamino, alkynylamino, cycloalkylamino, N-cycloalkyl-N-alkylamino, alkylideneamino or heterocyclyl, and R2 represents hydrogen or represents in each case optionally substituted alkyl, alkenyl, alkynyl or cycloalkyl, or R1 and R2 together with the nitrogen atom to which they are attached form an optionally substituted heterocyclic ring, R3 represents aryl which is optionally mono- to tetrasubstituted, R4 represents halogen, cyano or represents in each case optionally substituted alkoxy or dialkylamino and X represents halogen, a process for preparing these novel substances and their use for controlling unwanted microorganisms. Novel intermediates of the formulae and processes for their preparation.

Abstract: The invention concerns 1-H-3-arylpyrrolidine-2,4-dione derivatives of formula (I), in which A, B, G, X, Y and Z are as defined in the description, methods of preparing them and intermediates used in their preparation. The compounds of formula (I) are suitable for use as pest-control agents.

Abstract: The invention relates to novel halobenzenes, to a plurality of processes for their preparation and to their use for controlling harmful organisms, and also to novel intermediates and processes for their preparation.

Abstract: The invention relates to compounds of the formula (I), in which R1, R2, R3, R4, R5 and R6 are as defined in the disclosure, to a plurality of processes for their preparation, and to their use for controlling unwanted microorganisms.

Abstract: The invention relates to novel fungicidally active compound combinations of

Abstract: The invention relates to novel hydroxamic acid derivatives, to a plurality of processes for their preparation and to their use as pesticides.

Abstract: There are described new active compound combinations of a compound of the formula (I) 1

Abstract: Novel triazolopyrimidines of the formula 1

Abstract: The invention relates to novel fungicidally active compound combinations of (a) methoximinoacetamide derivatives of the general formula (I), in which R1 represents unsubstituted or fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i- or t-butyl-, methoxy-, ethoxy-, or phenoxy-substituted phenyl, 2-naphthyl, 1,2,3,4-tetrahydronaphthyl, indanyl, 2-benzofuranyl, 2-benzothienyl, 2-thienyl, or 2-furanyl, and (b) the active compound groups (I) to (58) listed in the disclosure.

Abstract: There are described new active compound combinations of a compound of the formula (I) with known fungicidal active compounds, and their use for the control of phytopathogenic fungi.

Abstract: Novel triazolopyrimidines of the formula 1

Abstract: The invention relates to novel heterocyclylphenyl benzyl ethers, to a process for their preparation and to their use for controlling harmful organisms.

Abstract: The invention concerns substituted spiro heterocyclic 1H-3-arylpyrrolidine-2,4-dione derivatives depicted by the formula: X is alkyl, halogen or alkoxy; Y is hydrogen, alkyl, halogen, alkoxy or alkyl halide; Z is alkyl, halogen or alkoxy; n is 0, 1, 2 or 3; G is hydrogen (a) or one of the groups (b), (c), (d), (e), (f) or (g) as defined in the specification. The invention also concerns methods of preparing the substituted spiro heterocyclic 1H-3-arylpyrrolidine-2,4-dione derivative compounds, intermediate compounds thereof and use of substituted spiro heterocyclic 1H-3-arylpyrrolidine-2,4-dione derivative compounds as pest-control agents.

Abstract: There are described new active compound combinations of a compound of the formula (I) with known fungicidal active compounds, and their use for combating phytopathogenic fungi.

Abstract: Novel triazolopyrimidines of the formula 1