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Matches 1,001 - 1,050 out of 7,343

Document Document Title
WO/2002/002515A1
Compounds useful in pest control, represented by the general formula [I] wherein A, B and C are each hydrogen, halogeno, trifluoro- methylsulfonyloxy, alkyl, alkylthioalkyl, or the like; X is a single bond, methylene, ethylene, or the li...  
WO/2002/000609A2
Formula (I) compounds are described where the groups are as defined in the description, as well as processes for their preparation and their use as medicaments, particularly for the preparation of medicaments with phosphodiesterase IV in...  
WO/2001/098250A1
New compounds of formula (I) are described. The compounds have potentially valuable pharmaceutical properties in the treatment of some central and peripheral nervous system disorders.  
WO2001039787A3
The invention relates to novel glyoxyl acid amides, a method for the production thereof and the use of said compounds to control harmful organisms.  
WO/2001/094298A1
The invention relates to a process for the production of cyclohexanone oxime in which a phosphate-containing aqueous reaction medium is cycled from a hydroxylammonium synthesis zone to a cyclohexanone oxime synthesis zone and back to the...  
WO/2001/094297A1
Process for the production of cyclohexanone oxime in which a phosphate-containing aqueous reaction medium is cycled from a hydroxylammonium synthesis zone to a cyclohexanone oxime synthesis zone and back to the hydroxylammonium synthesis...  
WO/2001/094296A1
The invention relates to a process for the production of cyclohexanone oxime in which a phosphate-containing aqueous reaction medium is cycled from a hydroxylammonium synthesis zone to a cyclohexanone oxime synthesis zone and back to the...  
WO/2001/094357A1
New spisulosine derivatives of use in treating tumors are of the formula (I) wherein: each X is the same or different, and represents H, OH, OR', SH, SR', SOR', SO¿2?R', NO¿2?, NH¿2?, NHR', N(R')¿2?, CN, halogen, C(=O)H, C(=O)CH¿3?,...  
WO/2001/092354A2
In the copolymerization of ethylene and acrylate esters, the use of selected acrylate esters suppresses the formation of acrylate ester homopolymer, and/or allows the rapid analysis by ?1¿H-NMR of the amount of homopolymer by product pr...  
WO/2001/092201A1
Novel substituted phenylpropionic acid derivatives of the general formula (1), which bind to human peroxisome proliferator activated receptor $g(a) (PPAR$g(a)) as ligand to activate the receptor and thereby exhibit a potent lipid-decreas...  
WO/2001/092342A2
Transition metal complexes of selected monoanionic phosphine ligands, which also contain a selected Group 15 or 16 (IUPAC) element and which are coordinated to a Group 3 to 11 (IUPAC) transition metal or a lanthanide metal, are po-lymeri...  
WO/2001/092347A2
Polymers are produced using transition metal complexes that have sites capable of binding a Lewis acid in close proximity to the metal center.  
WO/2001/090048A1
Process for removing a residual fragment of a chiral auxiliary from a diastereomeric compound with formula (2) in the preparation of an enantiomerically enriched, amine-functionalized compound, with the diastereomeric compound being subj...  
WO2000041476A3
Compounds of formula (I) wherein R1 is C1-C4-alkyl or cyclopropyl; R2 is C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkinyl; or C1-C6-alkyl substituted by 1 to 5 fluorine atoms; R3 is C1-C6-alkyl, C1-C6-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy...  
WO/2001/087826A1
The present invention relates to certain aryl cyclopropyl oxime ether and oxime amide compounds, compositions containing these compounds, and methods for controlling fungi by the use of a fungitoxic amount of these compounds.  
WO/2001/086057A1
The invention relates to an agent for coloring fibers, which is prepared before use by mixing an acidic component (A1), which contains at least one enamine of formula (I)/(Ia), with a component (A2), which contains a Schiff's base of for...  
WO/2001/085672A1
Compounds of general formula (I), where X = a CHO, CN, CH=NOH, or CH¿2?OH group and the C=C double bond may be either E or Z configuration are characterised by an interesting and original odour characteristic with high dispersion. Said ...  
WO/2001/082923A1
The present invention relates to compounds and derivatives thereof, their synthesis, and their use as estrogen receptor modulators. The compounds of the instant invention are ligands for estrogen receptors and as such may be useful for t...  
WO/2001/083571A2
Catalyst compositions useful for the polymerization or oligomerization of olefins are disclosed. Certain of the catalyst compositions comprise N-pyrrolyl substituted nitrogen donors. Also disclosed are processes for the polymerization or...  
WO/2001/083421A1
A process for the preparation of 2-halobenzoic acids of the general formula (I), characterized by reacting a benzoic acid of the general formula (II) with a halogenating agent in the presence of a Pd catalyst. [In the formulae, A is -OH,...  
WO/2001/081349A1
A novel, optically active, quaternary ammonium salt with axial asymmetry which is useful as a phase-transfer catalyst with which a glycine derivative is stereoselectively alkylated to convert it into an optically active $g(a)-amino acid ...  
WO/2001/080845A2
The subject invention provides compounds which are easily metabolized by the metabolic drug detoxification systems. Particularly, fluvoxamine analogs which have been designed to include esters within the structure of the compounds are ta...  
WO/2001/079157A1
Compounds having the formula are methionine aminopeptidase type 2 (MetAP2) inhibitors and are useful for inhibiting angiogenesis. Also disclosed are MetAP2-inhibiting compositions and methods of inhibiting angiogenesis in a mammal.  
WO/2001/079183A1
The invention relates to 2-phenyl-2H-pyridazine-3-ones of general formula (I), wherein the variables R?1¿, R?2¿ and X have the following meanings: X represents halogen; R?1¿ represents hydrogen or C¿1?-C¿4? alkyl, and; R?2¿ represe...  
WO/2001/077070A1
The invention relates to a method for producing oxime ethers of formula (I), in which the substituents R?1¿ and R?2¿ can be identical or different and can respectively represent cyano, alkyl, haloalkyl, cycloalkyl, phenyl and naphthyl ...  
WO2001038294A3
The invention relates to several novel methods for producing 2-(2-hydroxyphenyl)-2-(alkoxyimino)-N-methylacetamide derivatives, to novel intermediate products for their production, and to methods for producing these intermediate products.  
WO/2001/074760A1
The invention relates to a method for oximating organic carbonyl compounds and/or CH-acid compounds, wherein at least one organic carbonyl compound and/or CH-acid compound in a liquid or dissolved form is mixed with at least one oximatin...  
WO/2001/072695A1
Neovascularization inhibitors containing compounds of the general formula (II) or salts thereof are useful as preventive and therapeutic drugs for tumors and so on, wherein R?4¿ is an optionally substituted hydrocarbon group or the like...  
WO/2001/072854A2
Transition metal complexes of a monoanionic ligand derived from a selected o-(arylamino)benzalimine, and optionally in the presence of other cocatalysts, polymerize olefins. The resulting polymers are useful as elastomers and molding res...  
WO/2001/072680A1
This invention pertains to substituted chalcones, specifically substituted 1-(4-methoxyphenyl)-3-(3,5-dimethoxyphenyl)prop-1-en-3-ones, which have therapeutic application, for example, as potent antiproliferative agents and antiinflamma...  
WO/2001/072694A1
Zofimarin derivatives of the general formula (I), pharmacologically acceptable esters of the same, or salts thereof, exhibiting excellent antimycotic activity: (I) wherein X is formyl or cyano; and A is CH=N-O-R?a¿, -CH¿2?-S(=O)¿g?-R?...  
WO/2001/070676A1
New antitumor compounds isolated from a sponge are of the formulae (1), (2), (3) and (4).  
WO/2001/070675A2
The invention relates to the inhibition of histone deacetylase. The invention provides compounds and methods for inhibiting histone deacetylase enzymatic activity. The invention also provides compositions and methods for treating cell pr...  
WO/2001/070674A1
The invention refers to novel propenecarboxylic acid amidoxime derivatives furthermore N-oxides and/or geometrical isomers and/or optical isomers and/or pharmaceutically suitable acid addition salts and/or quaternary derivatives thereof....  
WO/2001/070677A1
A class of compounds is disclosed, comprising sulphonamido-substituted bridged bicycloalkyl structures of formula (I) (where the variables are as defined in the claims). The compounds are inhibitors of $g(g)-secretase, and hence are usef...  
WO/2001/070667A1
A compound represented by the formula (I) or a salt or solvate thereof; and a composition and a kit both containing any of these. In said formula X represents CH, sulfur, or nitrogen; Y represents CH, sulfur, or nitrogen or is absent; (a...  
WO/2001/068588A1
An $g(a)-iminoester derivative capable of being stably present under ordinary conditions; and a method of synthesizing various $g(a)-aminoester derivatives from the $g(a)-iminoester derivative in high yield. The derivative is a polymer-i...  
WO/2001/068724A2
Olefins, such as ethylene, are polymerized using as a polymerization catalyst a complex of a selected transition metal with an anionic ligand that has at least three atoms that may coordinate to the transition metal. Also disclosed are t...  
WO/2001/064646A2
Hydrazones and hydrazone analogs are provided which are useful as upregulators of LDL receptors and can be used in the treatment of hypercholesterolemia and related disorders and conditions.  
WO/2001/058848A1
The invention relates to a process for the purification of aminopropanediols having formula (I), in which D¿1? and D¿2? are independently H or CH¿2?OH, through the formation of the Schiff base of formula (III), obtained by reaction wi...  
WO/2001/056975A1
The invention concerns novel substituted imide derivatives of general formula (I), wherein R?1¿ represents optionally substituted cycloalkyl; R?2¿ represents optionally substituted alkyl or optionally substituted cycloalkyl; R?3¿ repr...  
WO2000002986A3
There is provided a process for producing particles of amine reaction product by means of a carrier having a melting point between 30 DEG C and 135 DEG C, optionally followed by a coating step. Processed amine reaction products and finis...  
WO/2001/055066A2
Compounds of general formula (I) wherein the substituents are as defined in claim 1 are suitable for use as herbicides.  
WO/2001/053254A1
Novel calcilytic compounds and methods of using them are provided.  
WO/2001/051453A1
Methods of making and using racemic and optically pure metabolites of sibutramine, and pharmaceutically acceptable salts, solvates, and clathrates thereof, are disclosed. Pharmaceutical compositions and dosage forms are also disclosed wh...  
WO2001002370A9
The invention relates to a compound comprising a labeled nickel complex (Figure 1) that is used to detect and purify nucleic acid sequences by forming an adduct between a specific nucleic acid base and the labeled nickel complex. The add...  
WO2001042196A8
The present invention provides an ester compound encompassed by formula (I) wherein R<1> represents a hydrogen atom, a C1 to C5 alkyl group which may be substituted with at least one halogen atom, a C4 to C5 cycloalkyl group which may be...  
WO/2001/045696A1
The use of a mono-cationic salt of N,N'-bis(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED) in iron chelating therapy is disclosed. In particular, the invention relates to the intravenous use of a mono-cationic salt of HBED for...  
WO/2001/046114A1
The preparation of mono-cationic salt of N,N'-bis(2-hydroxybenzyl)- ethylenediamine-N,N'-diacetic acid (HBED) and HBED itself is disclosed. In particular, the invention relates to the hydrolysis of the t-butyl ester of HBED with a weak a...  
WO/2001/043712A1
The invention relates to cosmetic and/or dermatological preparations which contain, in part, novel catechol oximes of formula (I). Said preparations can promote, in physiological systems, the natural defense mechanisms against free radic...  

Matches 1,001 - 1,050 out of 7,343