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

Abstract: Novel silylated carboxamides of the formula (I) in which M, L, R1, R2, R3, R and A are as defined in the description, a plurality of processes for preparing these compounds and their use for controlling unwanted microorganisms, and also novel intermediates and their preparation.

Abstract: This invention relates to triazolopyrimidines-of the formula in which R1, R2, R3, R4 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 invention relates to new triazolopyrimidines of the formula in which R1, R2, R3 and X have the meanings specified 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 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: 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: This invention relates to novel pyrazolopyrimidines of the formula in which R1, R2, R3, R4, R5, R6, R7 and R8 are as defined in the disclosure, to a plurality of processes for preparing these compounds and to their use for controlling unwanted microorganisms.

Abstract: This invention relates to imidazolopyrimidines 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 invention relates to novel triazolopyrimidines of formula (I), in which R1, R2, R3 and X are defined as cited in the description, to a method for producing said substances and to their use for controlling undesirable micro-organisms. The invention also relates to novel intermediate products of the formulae (II), (VI), (VII-a) and (VII-b), in addition to methods for producing said substances.

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: 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: 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 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: Novel triazolopyrimidines of the formula 1

Abstract: Novel triazolopyrimidines of the formula 1

Abstract: The present invention relates to methods for identifying fungicides and also inhibitors of the 20S and 26S proteasomes, to methods for isolating 20S proteasomes, to the use of 20S proteasomes for identifying fungicides and to the use of the inhibitors of 26S and/or 20S proteasomes as fungicides.