Abstract: The invention relates to novel triazolopyrimidines of the formula in which R1, R2, R3 and X have the meanings given in the disclosure, and acid addition salts thereof, to a plurality of processes for preparing these novel substances, and to their use for controlling unwanted microorganisms. The invention further relates to novel amines and carbamates of the formulae indicated in the description and to processes for preparing these intermediates.

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: New pyrazolopyrimidines of the formula in which R1, R2, R3, R4, X and Hal have the meanings specified in the description, multiple methods for producing these materials and their use for combating undesired micro-organisms. New intermediate products of the formulas and methods for producing these materials.

Abstract: The invention relates to new triazolopyrimidines of the formula in which R1, R2, R3, G and X have the meanings given in the description, a process for preparing these substances and their use for combating undesirable micro-organisms. The invention further relates to new intermediate products of the formulae and processes for preparing these substances.

Abstract: Novel pyrazolopyrimidines of the formula in which R1, R2, R3, R4, R5 and R6 are as defined in the description, a plurality of processes for preparing these compounds and their use for controlling unwanted microorganisms.

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: The present invention relates to a novel active compound combination for controlling phytopathogenic fungi which comprises two oxime ether derivatives and a hydroxyethyltriazole derivative.

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 relates to prazolopyrimidines of the formula in which R1, R2, R3, R4, R5, and X are as defined in the disclosure, to a process for preparing these compounds, and to their use for controlling unwanted microorganisms.

Abstract: The present invention relates to novel 5-phenylpyrimidines, to a plurality of processes for their preparation, and to their use for controlling unwanted microorganisms. The invention further relates to novel intermediates and to processes for their preparation.

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 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: 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: The invention relates to novel gloyoxylic acid amides, to a process for their preparation and to their use for controlling harmful organisms.

Abstract: Novel triazolopyrimidines of the formula 1