Document |
Document Title |
WO/1999/009008A1 |
The invention relates to a method for producing an organic compound of formula (I) and optionally its E/Z-isomers, E/Z-isomer mixtures and/or tautomers, each in free or salt form, R¿1? representing hydrogen or C¿1?-C¿4? alkyl, R¿2? r...
|
WO/1999/009009A1 |
The invention relates to a method for producing compounds of formula (I), wherein R¿1? is hydrogen or C¿1?-C¿4? alkyl, R¿2? is hydrogen, C¿1?-C¿6?alkyl, C¿3?-C¿6? cycloalkyl or a radical -CH¿2?B, A is an unsubstituted or substit...
|
WO/1999/005127A1 |
A compound of formula (I), wherein R?1¿ and R?2¿ are independently selected from saturated fluorocarbon substituted side chains, such as NR?5¿(CH¿2?)¿n?C¿m?F¿2m+1?, O(CH¿2?)¿n?C¿m?F¿2m+1?, S(CH¿2?)¿n?C¿m?F¿2m+1?, NR?5¿S(O...
|
WO/1999/001510A1 |
Compounds of Formula (1) wherein: A is N, C-CI, C-CN or C-NO¿2?; L?1¿ is -OR?3¿; Z is -O-, -S- or -NR?2¿-; R?1¿ and R?2¿ are each independently H or optionally substituted alkyl; R?3¿ is H or alkyl; each W independently is -CO¿2?...
|
WO/1999/001442A1 |
Compounds of formula (I), pharmaceutically acceptable salts or $i(in vivo) hydrolysable esters thereof, wherein: X is O, NH, CH¿2?; R?1¿ is an optionally substituted aryl ring, optionally substituted heteroaryl ring, or such ring syste...
|
WO/1999/001376A1 |
The present invention provides a method and composition regeneration of an aminal that has previously been reacted with a sulfide selected from hydrogen sulfide and mercaptans. The method includes contacting a scavenging mixture which in...
|
WO/1999/001439A1 |
Corticotropin releasing factor (CRF) antagonists of formula (I), and their use in treating psychiatric disorders and neurological diseases, anxiety-related disorders, post-traumatic stress disorder, supranuclear palsy and feeding disorde...
|
WO/1999/000374A1 |
High pressure melamine manufacturing process starting from urea with high yields and conversion rates characterized in that it comprises the following steps: a) urea is fed to a reactor essentially containing molten melamine, which react...
|
WO/1998/058916A1 |
The invention relates to carboxylic acid derivatives of formula (I) wherein the constituents have the meaning given in the description. The invention also relates to the production of said derivatives, and to their use as endothelin rece...
|
WO/1998/055461A1 |
The invention relates to novel fluoromethoximino compounds, methods for producing the same and their use as pest-control agents, as well as to new intermediate products and several methods for producing said products.
|
WO/1998/055464A1 |
Fluoropolyether compounds of general formula (I) wherein Rf's may be the same or different and each represents a group of the following general formula (II): X-(CH�2?CF�2?CF�2?O)�a?- (CHClCF�2?CF�2?O)�b?-(CCl�2?CF�2?CFï...
|
WO/1998/055465A1 |
Multicrystalline melamine powder having the following properties : d�90?: 50-150 $g(m)m; d�50? < 50 $g(m)m; bulk density (loose) 430-570 kg/m?3�; color APHA less than 17; melamine: > 98.5 wt.%; melam: < 1 wt.%. Multicrystalline mel...
|
WO/1998/055466A1 |
Method for preparing melamine from urea via a high-pressure process in which solid melamine is obtained by transferring the melamine melt coming from the reactor to a vessel where the melamine melt is cooled with an evaporating cooling m...
|
WO/1998/054160A1 |
Method for preparing melamine from urea via a high-pressure process in which solid melamine is obtained by transferring the melamine melt coming from the reactor to a vessel where the melamine melt is cooled with an evaporating cooling m...
|
WO/1998/053369A1 |
Novel water-soluble triazine photoinitiators and bifunctional ionic photoinitiators having an anion containing a photo-labile halomethyl-1,3,5-triazine and a photoinitiator cation are described. The ionic compounds are good photoinitiato...
|
WO/1998/052551A1 |
Cancer remedies, each containing a compound of the following general formula (I): Ar?1�-S-R?1�-S-Ar?2� [wherein RP represents a non-metallic connecting group; Ar?1� and Ar?2� each independently represents aryl or heteroaryl hav...
|
WO/1998/052928A1 |
Method for preparing melamine from urea via a high-pressure process in which solid melamine product is obtained directly from the melamine melt by transferring the melamine melt into a product cooling unit where it is cooled with ammonia...
|
WO/1998/052915A2 |
The invention relates to leukotriene B�4? derivatives of general formula (I) in which R�1? stands for H, CF�3?, CH�2?OH; R�2? stands for an organic acid radical; R�3? stands for H, C�1?-C�14?-alkyl, C�3?-C�10?-cycloal...
|
WO/1998/052942A1 |
A compound, or a solvate or a salt thereof, of formula (I): wherein, Ar is an optionally substituted aryl or a C�5-7? cycloalkdienyl group, or a C�5-7? cycloalkyl group or an optionally substituted single or fused ring aromatic heter...
|
WO/1998/049150A1 |
The present ivnention relates to a partially hydrogenated or completely hydrogenated 1,3,5-triazine derivative which has (i) a group of formula (a), wherein Q?1� represents an aromatic ring group which may optionally be substituted; R?...
|
WO/1998/046342A2 |
A description is given of an extrusion process for the preparation of a low-dust stabiliser, using a subcooled melt as granulation liquid, as well as of amorphous modifications of different stabilisers, including 2,2'-methylenebis(4-[1,1...
|
WO/1998/044007A1 |
A radiation-polymerizable composition contains at least one radiation curable acrylate resin oligomer prepared by reacting an alkoxylated polyol with a first acid component which includes an ethylenically unsaturated carboxylic acid; and...
|
WO/1998/042684A1 |
The invention relates to novel substituted 2,4-diamino-1,3,5-triazines of formula (I), wherein R?1� stands for (respectively unsubstituted ) phenyl or naphthyl, R?2� stands for alkyl, R?3� represents hydrogen, halogen or respective...
|
WO/1998/042685A1 |
The present invention provides new compounds having formula (1), in which X is O or, preferably, NH; M is hydrogen, an alkali metal atom, ammonium or a cation formed from an amine; each R�1?, independently, is an aminoacid residue from...
|
WO/1998/041206A1 |
This invention provides a method for treating cancer in an individual, wherein the cancer is a tumor in which endothelin is upregulated (e.g. tumors of the prostate, lung, liver, breast, brain, stomach, colon, endometrium, testicle, thyr...
|
WO/1998/040361A1 |
Aminosulfonylureas of general formula (I). The aminosulfonylureas of said formula are endowed with a high herbicidal activity against numerous weeds.
|
WO/1998/039308A1 |
A compound of formula (I) wherein: R?1� and R?2� each independently represents arylamino, diphenylamino, benzylamino or dibenzylamino, and Z represents a leaving group. In general the group -SO�2?-CH�2?-CH�2?-Z is a blocked vin...
|
WO/1998/038172A1 |
The invention relates to new phenyl-amino-sulfonyl-urea derivatives, a method for producing said derivatives, and the use thereof as fungicides.
|
WO/1998/038188A1 |
Novel herbicidal compounds, compositions containing them, and methods for their use in controlling weeds are disclosed. The novel herbicidal compounds are represented by formula (I), where J is a 1-substituted-6-trifluoromethyl-2,4-pyrim...
|
WO/1998/035944A1 |
$g(a)-alkoxy and $g(a)-thioalkoxyamide compounds of formula (I) and methods of administering the compositions to mammals to treat disorders such as obesity that are mediated by NPY and especially those mediated by NPY via the Y5 receptor...
|
WO/1998/035930A1 |
Process for the preparation of an N-acyl amino carboxylic acid by means of a carboxymethylation reaction. In this reaction, a reaction mixture is formed which contains a base pair, carbon monoxide, hydrogen and an aldehyde with the base ...
|
WO/1998/034925A1 |
Some 2-amino-4-(phenoxyethylamino)-1,3,5-triazines substituted in 6-position are known to possess herbicidal and plant-growth regulating properties, cf. WO 90/09378, WO 94/24086 and WO 96/25404. The invention describes structurally diffe...
|
WO/1998/034926A1 |
A compound of formula (1) and salts thereof, wherein Ar, Ar?1�, J, J?1�, X, X?1�, W, W?1�, L and m are as defined in the description. The compounds of formula (1) are useful as additives in inks, especially ink jet printing inks,...
|
WO/1998/032718A1 |
The properties of biologically active compounds, for example drugs and agrochemicals, which contain in their molecular structure one or more functional groups selected from alcohol, ether, phenyl, amino, amido, thiol, carboxylic acid and...
|
WO/1998/032743A1 |
The invention concerns compounds of formula (I) and their salts, in the formula R?1�-R?9�, W and A being defined as in formula (I) according to claim 1. These compounds and salts are suitable as herbicides and plant-growth regulators...
|
WO/1998/030719A1 |
Reagents capable of forming branched oligomers with monomeric units are disclosed, together with oligomers incorporating such reagents, kits containing such reagents and methods for use of such reagents in forming oligomers with monomeri...
|
WO/1998/029399A1 |
The invention relates to ionic compounds in which the anionic load has been delocalized. A compound disclosed by the invention includes an anionic portion combined with at least one cationic portion M?+m� in sufficient numbers to ensur...
|
WO/1998/029388A1 |
The invention relates to ionic compounds in which the anionic load has been delocalized. A compound disclosed by the invention is comprised of an amide or one of its salts, including an anionic portion combined with at least one cationic...
|
WO/1998/029877A1 |
Disclosed is a proton conductor in liquid form, comprised of a mixture of the following components: (a) a salt combined with a nitrogenated base along with an acid, according to formula (I), wherein Z�1?, Z�2?, Z�3?, and Z�4?, wh...
|
WO/1998/029389A1 |
The invention is related to ionic compounds, derivatives of malononitrile, in which the anionic load has been displaced. An ionic compound disclosed by the invention includes an anionic portion combined with at least one cationic portion...
|
WO/1998/029396A1 |
The invention relates to ionic compounds in which the anionic load has been displaced, and the uses of these compounds. A compound disclosed by the invention comprises an anionic portion combined with at least one cationic portion M?+mï¿...
|
WO/1998/029358A2 |
Disclosed is a method for grafting a polymer onto the surface of a carbonate material with carboxyl, amine, and/or hydroxyl functions on its surface. Said material is placed in suspension in a solution including the polymer to be grafted...
|
WO/1998/027071A1 |
The invention relates to a method for the preparation of melamine from urea in which solid melamine is obtained by transferring the melamine stream leaving the reactor to a product cooling unit where the melamine stream is cooled to a te...
|
WO/1998/022447A1 |
A description is given of symmetrical triazine derivatives of formula (1), wherein R�1? and R�2? are each independently of the other hydrogen; C�1?-C�12?alkyl, C�1?-C�12?alkoxy; and R�3? is C�1?-C�12?alkyl; or C�1?-Cï...
|
WO/1998/021963A1 |
Novel agrichemical quaternary salts, compositions and a method to prepare them are disclosed.
|
WO/1998/021191A1 |
Cyanoethylmelamine derivatives represented by general formula (I) wherein one to five of the substituents X?1� to X?6� each represents cyanoethyl; at least one remaining substituent represents C�1-20? alkyl, C�2-20? alkenyl (the ...
|
WO/1998/021190A1 |
This invention provides compounds of formula (1) having the structure wherein R?1�, R?2�, R?3�, R?4�, and R?5� are each independently, hydrogen, halogen, alkyl, cycloalkyl, alkenyl, alkynyl, phenylalkyl, alkoxy, aryloxy, fluoro...
|
WO/1998/017630A1 |
The invention relates to novel amides of the general formula (I), a method for their production and their use as pesticides.
|
WO/1998/016515A1 |
There is disclosed pharmaceutical compositions that possess anti-infective activity against HIV virus and certain parasites. The pharmaceutical compositions comprise oral formulations having an active arylene bis (methyl carbonyl) deriva...
|
WO/1998/015540A1 |
The invention relates to X�n?(alkoxy)�(6-n)?alkyl melamine, in which X = halide, n = 1-6, and the alkoxy group and the alkyl group contain 1 to 6 carbon atoms, a process for the preparation of these compounds and the use of these com...
|