Abstract: The invention relates to a conveyor system for conveying products (18) to be conveyed, in particular for conveying food products, with at least one conveyed-products carrier (4) for receiving the products (18) to be conveyed, and a drive system (17) for discontinuously conveying the conveyed-products carrier (4) within a conveying surface (9) along a conveying path. The invention provides that the drive system (17) angles the conveyed-products carrier (4) to the conveying surface (9).

Abstract: The invention relates to a food-processing device for cutting food products (2) into slices (6), the slices (6) preferably together forming a portion, in particular for cutting pieces of meat or pieces of cheese. The food-processing device according to the invention comprises a cutting device (1) for cutting the slices (6) from the food products (2), and a conveyor (AS, 12-18) for receiving the cut slices (6) after a cutting operation, wherein the conveyor (AS, 12-18) is preferably arranged in the line of fall of the slices (6), so that the cut slices (6) fall from the cutting device (1) onto the conveyor (AS, 12-18). The invention provides that the conveyor (AS, 12-18) is a discontinuous conveyor, which conveys the deposited slices (6) discontinuously, in contrast to a conveyor belt. Furthermore, the invention comprises a corresponding operating method.

Abstract: The invention relates to a belt conveyor (1) for conveying products to be conveyed (e.g. food products), with a deflection (8), in particular as a rotatable deflection pulley (8), and a conveyor belt (2) which is guided around the deflection (8). The invention provides that the deflection (8) comprises a central circumferential annular groove (11), and the conveyor belt (2) comprises a centre bar (12) on the inside which engages in the annular groove (11) of the deflection (8).

Abstract: The invention relates to a conveying device for conveying food products in a food processing installation, having at least one movable conveyed-product carrier (12, 13; 30, 31) for receiving the food products to be conveyed, and a drive system (15-18) for conveying the conveyed-product carrier (12, 13; 30, 31) discontinuously along a conveying path (27). The invention additionally provides a cleaning device (32) for cleaning the conveyed-products carrier (12, 13; 30, 31) and/or the conveying path (27).

Abstract: The present invention relates to a process for preparing 4-{4-[({[4-chloro-3-(trifluoro-methyl)phenyl]amino}carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxamide and its tosylate salt.

Abstract: The present invention relates to a process for preparing 4-{4-[({[4-chloro-3-(trifluoro-methyl)phenyl]amino}carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxamide and its tosylate salt.

Abstract: The present invention relates to a novel process for preparing 8-methoxy-3-quinolonecarboxylic acids which are antibiotics having potent antibacterial action.

Abstract: A gas collection pipe (1) carrying hot gas establishes the connection between the combustion chambers (9) of a gas turbine plant and the flow channel (13) of the gas turbine. The gas collection pipe (1) has two inlet pipe connections (2), which open via an elbow (3) axially into a gas ring channel (4), which is joined to the flow channel (13). Cooling air is guided on the outside along the elbow (3). A plurality of ribs (8) are arranged at spaced locations from one another on the outside on the gas collection pipe (1) in the area of the elbow (3) on the side facing away from the flow channel (13).

Abstract: The present invention relates to a novel process for preparing 8-methoxy-3-quinolonecarboxylic acids which are antibiotics having potent antibacterial action.

Abstract: The present invention relates to a novel process for preparing 8-methoxy-3-quinolonecarboxylic acids which are antibiotics having potent antibacterial action.

Abstract: A gas collection pipe (1) carrying hot gas establishes the connection between the combustion chambers (9) of a gas turbine plant and the flow channel (13) of the gas turbine. The gas collection pipe (1) has two inlet pipe connections (2), which open via an elbow (3) axially into a gas ring channel (4), which is joined to the flow channel (13). Cooling air is guided on the outside along the elbow (3). A plurality of ribs (8) are arranged at spaced locations from one another on the outside on the gas collection pipe (1) in the area of the elbow (3) on the side facing away from the flow channel (13).

Abstract: The present invention relates to a novel process for preparing 8-methoxy-3-quinolonecarboxylic acids which are antibiotics having potent antibacterial action.

Abstract: The invention relates to phenylacetic acid derivatives which are substituted by a five-membered nitrogen heterocycle bonded via an N atom. They are prepared by reaction of phenylacetic acid derivatives substituted with leaving groups with the appropriate nitrogen heterocycles and can be used as active substances in medicaments for the treatment of high blood pressure and atherosclerosis.

Abstract: The invention relates to phenylacetic acid derivatives of the formula ##STR1## which are substituted by a five-membered nitrogen heterocycle bonded via an N atom. They are prepared by reaction of phenylacetic acid derivatives substituted with leaving groups with the appropriate nitrogen heterocycles and can be used as active substances in medicaments for the treatment of high blood pressure and atherosclerosis.

Abstract: New phenylsulphonamide of the formula in which ##STR1## R.sup.1 represents a pyridyl, quinolyl or isoquinolyl radical which is unsubstituted or substituted by halogen, alkyl, cycloalkyl, alkoxy, cyano, nitro, halogenoalkyl, halogenoalkoxy, alkoxycarbonyl or alkylsulphonyl,R.sup.2 represents hydrogen, cyano, nitro, halogen, alkyl, alkoxy, halogenoalkyl, halogenoalkoxy or alkoxycarbonyl,R.sup.3 represents an aryl radical which is unsubstituted or monosubstituted, disubstituted or trisubstituted by halogen, halogenoalkyl, halogenoalkoxy, alkyl, alkoxy, alkylthio, alkylsulphonyl, cyano, nitro or alkoxycarbonyl, the substituents being identical or different, or represents pentafluorophenyl or represents a straight-chain, branched or cyclic alkyl which is unsubstituted or substituted by halogen, aryl, aryloxy, cyano, alkoxycarbonyl, alkoxy, alkylthio or trifluoromethyl, andX represents an --O--, --A--B-- or --B--A-- group, whereA denotes ##STR2## and B denotes ##STR3## where R.sup.

Abstract: For inhibiting lipoxygenzce, (quinolin-2-yl-methoxy) phenylacetic acid derivatives containing cyclic substituents of the formula ##STR1## in which A, Q, D, E, G, T and M are hydrogen or various radicals,R.sup.3 is halogen or an alkyl or phenyl radical, andR.sup.1 and R.sup.2 complete a carbocyclic ring which may be substituted and/or fused to another ring,and salts thereof.

Abstract: Inhibiting leucotriene synthesis in patients with novel substituted N-(quinolin-2-yl-methoxy)benzylsulphonyl-urea of the formula ##STR1## in which A, B, D, E, G, K and M each independently is H, OH, halogen, CF.sub.3, OCF.sub.3, COOH, alkyl, alkoxy, alkoxycarbonyl or aryl,R.sup.1 is alkyl or cycloalkyl,R.sup.2 and R.sup.3 each independently is H or alkyl, andR.sup.4 is alkyl, aryl or a heterocyclic radical,and salts thereof.

Abstract: Inhibiting leucotriene synthesis in patients with novel disubstituted (quinolin-3-yl-methoxy)phenylacetic acid derivatives of the formula ##STR1## in which A, B, D, E, G, K and M each independently is H, OH, halogen, CF.sub.3, OCF.sub.3, COOH, alkyl, alkoxycarbonyl or aryl,R.sup.1 is alkyl or cycloalkyl,R.sup.2 and R.sup.3 each independently is H, alkyl or aryl, andX is O or S,and salts thereof.

Abstract: Substituted (quinolin-2-ylmethoxy)phenyl-thio-ureas of the formula ##STR1## in which A, B, D, E, G, K and Mrepresent hydrogen, hydroxyl, halogen, carboxyl, nitro, trifluoromethyl or trifluoromethoxy, orrepresent alkyl, alkoxy or alkoxycarbonyl, orrepresent aryl, which is optionally substituted by halogen, hydroxyl, nitro or cyano,R.sup.1represents hydrogen or alkyl, which is optionally substituted by aryl or cycloalkyl, orrepresents cycloalkyl,R.sup.2represents alkyl, which is optionally substituted by halogen or hydroxy, orrepresents cycloalkyl, which is optionally substituted by halogen or cyano, orrepresents aryl which is optionally substituted by halogen, nitro, cyano, alkyl, or by --SO.sub.2 --R.sup.3, in whichR.sup.3 denotes alkyl or --NR.sup.4 R.sup.5, in whichR.sup.4 and R.sup.5 denote hydrogen, alkyl or phenyl,orR.sup.2 represents --CO--R.sup.6, in whichR.sup.

Abstract: New phenylsulphonamides of the formula in which ##STR1## R.sup.1 represents a pyridyl, quinolyl or isoquinolyl radical which is unsubstituted or substituted by halogen, alkyl, cycloalkyl, alkoxy, cyano, nitro, halogenoalkyl, halogenoalkoxy, alkoxycarbonyl or alkylsulphonyl,R.sup.2 represents hydrogen, cyano, nitro, halogen, alkyl, alkoxy, halogenoalkyl, halogenoalkoxy or alkoxycarbonyl,R.sup.3 represents an aryl radical which is unsubstituted or monosubstituted, disubstituted or trisubstituted by halogen, halogenoalkyl, halogenoalkoxy, alkyl, alkoxy, alkylthio, alkylsulphonyl, cyano, nitro or alkoxycarbonyl, the substitutents being identical or different, or represents pentafluorophenyl or represents a straight-chain, branched or cyclic alkyl which is unsubstituted or substituted by halogen, aryl, aryloxy, cyano, alkoxycarbonyl, alkoxy, alkylthio or trifluoromethyl, andX represents an --O--, --A--B-- or --B--A-- group, whereA denotes --O--, ##STR2## B denotes --O--; ##STR3## where R.sup.