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Matches 1 - 50 out of 8,753

Document Document Title
WO/2018/108925A1
A sulfonic acid salt composition comprises compounds of formula (I), wherein n is 1 or 2,R1 is H or C1-C6 alkyl, R2 is COOM, SO3M or CH(OH)SO2-OM, each M is an equivalent of a multivalent metal, preferably magnesium, calcium, aluminum, z...  
WO/2018/108922A1
The invention relates to mixed salts of hydroxyalkane sulfinic acids and optionally hydroxyalkane sulfonic acids, their preparation and the use of said salts as reducing agent. The reducing power of the salts of the invention is signific...  
WO/2017/099662A1
A method for producing derivatives of N-retinoylaminoalkane sulfonic acid, the method comprising providing retinoic acid, chloroformate, aminoalkanesulfonic acid selected from the group consisting of cysteic acidand alkyl ester thereof, ...  
WO/2017/051326A1
The invention relates to a novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active compounds, in particular neutral endopeptidase (NEP) inhibitors such as sacubitril, and prodrugs the...  
WO/2016/143634A1
Provided is a bimesogenic compound which exhibits high solubility in other bimesogenic compounds and substances used in conventional liquid crystal display elements, such as liquid crystalline compounds, liquid crystal compositions, chir...  
WO/2016/142315A1
The invention relates to a process for preparing an oxysulphide and fluorinated compound, which comprises reacting, in the presence of an organic solvent, at least one compound of formula Ea-X (I), in which Ea is a fluorine atom or a gro...  
WO/2016/091772A1
The invention relates to a method for producing an oxysulphidic and fluorinated derivative in the form of a salt of formula (II) Ea-SOO-Q+ (II) comprising providing an ionic liquid compound of formula (I) in the liquid state Ea-SOO-Q+ (I...  
WO/2015/087352A1
The present patent discloses a novel, efficient and transition-metal-free room temperature single step process for synthesis of aryl sulfones and substituted aryl sulfones starting from aryl substrates.  
WO/2015/060402A1
 Provided are a novel production method for trifluoromethanesulfonanilides, which are useful as herbicides, etc., and intermediates therefor. Specifically provided are: an industrially-useful production method for producing a trifluo...  
WO/2015/036504A1
The invention concerns a method for preparing an oxysulphide and fluorinated derivative, said method comprising the reacting, in the presence of an organic solvent, of: i) at least one compound of formula Ea-COOR (I), in which Ea represe...  
WO/2014/186571A1
Bezoxazole sulfenamide accelerators are provided. The bezoxazole sulfenamide accelerators may be used in cure system for the vulcanization of rubber. The bezoxazole sulfenamide accelerators may also be used in asphalt and polymer composi...  
WO/2014/081558A1
Disclosed is a process for making diastereomeric N-sulfinyl α-amino amides by reaction of chiral sulfinimines with formamides and lithium diisopropylamide. The process of the invention provides the N-sulfinyl α-amino amides in high yie...  
WO/2014/070215A1
Provided herein are novel chiral sulfinamide and imine compounds. Also provided herein are methods of synthesizing novel chiral sulfinamide and imine compounds comprising simplified purification methods when compared to prior methods. Th...  
WO/2013/124230A1
The invention relates to sulfinimidoyl- and sulfonimidoylbenzoyl derivatives of the general formula (I). In said formula (I), R, R', X, W and Z represent radicals such as hydrogen, organic radicals such as alkyl, and other radicals such ...  
WO/2013/100158A1
An actinic ray-sensitive or radiation-sensitive resin composition, which is excellent in sensitivity, resolution, a pattern profile and a depth of focus (DOF), and, an actinic ray-sensitive or radiation-sensitive film and a pattern formi...  
WO/2012/166578A3
Described herein are allyl ether-terminated fluoroalkylsulfinic acids and salts thereof and methods of making.  
WO/2012/166578A2
Described herein are allyl ether-terminated fluoroalkylsulfinic acids and salts thereof and methods of making.  
WO/2012/097550A1
Cyclohydrocarbyl formamide derivatives of general formula (I), preparation methods and uses thereof are provided. The present cyclohydrocarbyl formamide derivatives of general formula (I) target on the auxiliary protein Vif (Virus infect...  
WO/2012/090959A1
The purpose of the present invention is to meet the increasing demands on fine patterns in the microfabrication field, including the manufacture of integrated-circuit elements, by providing: a radiation-sensitive resin composition that n...  
WO/2012/082695A3
There is provided a process for preparing a perfluorovinyl ether sulfinate, comprising: a) providing a perfluorovinyl ether sulfonyl halide; and (b) reducing the perfluorovinyl ether sulfonyl halide with a reducing agent in an organic pr...  
WO/2012/082695A2
There is provided processes for preparing a perfluorovinylether sulfinate.  
WO/2012/082703A2
There is provided a method for preparing oligomers and co-oligomers of highly fluorinated sulfinic acids and salts thereof.  
WO/2012/082703A3
There is provided a method for preparing oligomers and co-oligomers of highly fluorinated sulfinic acids and salts thereof.  
WO/2011/143376A1
An odor control composition includes (a) at least one fragrance and (b) a halo active aromatic sulfonamide compound of Formula (I): wherein R1, R2, R3, R4, and R5 are independently selected from hydrogen, COOR', CON(R")2, alkoxy, CN, NO2...  
WO/2011/110653A1
Solution of conductive molecular materials and electromagnetic absorbents produced from these solutions. The invention relates to a stable solution of molecular material, characterized in that it comprises: - a first type of organic or o...  
WO/2011/108622A1
Disclosed is a preparation method for obtaining an alkali metal perfluorosulfinate by reacting a perfluoroalkane sulfinyl halide with a sulfur-containing reducing agent in the presence of water, wherein mineral salts, which are an impuri...  
WO/2011/098417A1
Substituted cyanobutyrates of the formula I in which the variables are defined according to the description, processes and intermediates for preparing the compounds of the formula I and their N-oxides, their agriculturally suitable salts...  
WO/2011/080752A1
A process for the preparation of perfluoroalkyl sulfenyl chloride; said process comprising i) reacting a compound of formula (I) wherein R represents an aromatic group with or without a substituent; and R' represents a halogen, with at l...  
WO/2011/060113A1
The invention relates generally to optical agents for biomedical applications, including phototherapy. Provided are sulfenamide compounds having an acyclic S-N bond with at least one aromatic and/or heterocyclic aromatic group providing ...  
WO/2011/012248A3
The invention relates to 2-(3-aminobenzoyl)-3-cyclopropyl-3-oxopropane nitriles of general formula (I) as herbicides. In said formula (I), X and Y are organic groups such as alkyl and other groups such as halogen, nitro and cyano.  
WO/2011/012248A2
The invention relates to 2-(3-aminobenzoyl)-3-cyclopropyl-3-oxopropane nitriles of general formula (I) as herbicides. In said formula (I), X and Y are organic groups such as alkyl and other groups such as halogen, nitro and cyano.  
WO/2010/132982A1
It is reported herein that certain muscle diseases and conditions, including forms of muscular dystrophy, are characterized by impaired insulin-dependent signaling in the muscle tissue, in essence, a form of insulin resistance. The prese...  
WO/2010/127991A1
The present invention relates to a method for preparing fluoroalkanesulphinic acid esters. The invention specifically relates to the preparation of esters of trifluoromethanesulphinic acid, commonly referred to as "triflinic acid". The m...  
WO/2010/104177A1
A fluoroalkanesulfinic acid ammonium salt is obtained using an organic base when a bromofluoroalkyl carboxylate ester is sulfinated using a sulfinating agent. The fluoroalkanesulfinic acid ammonium salt is oxidized, thereby obtaining a f...  
WO/2010/104178A1
An ammonium hydroxyfluoroalkanesulfinate is obtained by using an organic base while sulfinating a bromofluoroalcohol with a sulfinating agent. An ammonium hydroxyfluoroalkanesulfonate is obtained by oxidizing said ammonium hydroxyfluoroa...  
WO/2010/100337A1
The present invention relates to novel prodrugs of metformin, their pharmaceutically acceptable salts, pharmaceutical compositions containing the prodrugs, and methods of using the prodrugs. In particular, the present invention relates t...  
WO/2010/096677A3
Compounds are provided that comprise dinitroso-derivatives of dihydrolipoic acid. Pharmaceutical compositions comprising the compounds and methods of using the compounds for treating various diseases and disorders, including angina, hype...  
WO/2010/096677A2
Compounds are provided that comprise dinitroso-derivatives of dihydrolipoic acid. Pharmaceutical compositions comprising the compounds and methods of using the compounds for treating various diseases and disorders, including angina, hype...  
WO/2010/050392A1
An aimed alkoxycarbonylfluoroalkanesulfonic acid salt is obtained by using a halofluoroalkanoic acid ester as a starting raw material, and by sulfinating the ester in the presence of an amine (step 1) and then oxidizing the resulting pro...  
WO/2010/037693A1
The invention relates to a method for purifying trifluoromethanesulfinic acid by azeotropic distillation using an aromatic solvent, to a method for producing purified trifluoromethanesulfinic acid, and to the use of the purified trifluor...  
WO/2010/013687A1
A perfluoroalkanesulfonyl halide is reacted with hydrazine to obtain a perfluoroalkanesulfinic acid hydrazine salt (RfSO2H·N2H4). The hydrazine salt obtained is reacted with a base such as an alkali metal hydroxide to obtain a perfluor...  
WO/2009/133052A1
The present invention relates to a compound of formula (I), including any stereochemically isomeric form thereof, wherein the substituents are as defined in the specification and the claims; a N-oxide thereof, a pharmaceutically acceptab...  
WO/2009/128907A1
Processes useful for making a pharmaceutically useful compound according to Formula (I), forms of such a compound, and intermediates useful in such processes are described.  
WO/2009/099902A1
Described herein are compounds that are antagonists of PGD2 receptors. Also described are pharmaceutical compositions and medicaments that include the compounds described herein that are antagonists of PGD2 receptors. Also described here...  
WO/2009/068533A1
The present invention relates to a method for preparing a highly pure trifluoromethanesulphinic acid. The method of the invention for preparing a highly pure trifluoromethanesulphinic acid, starting from an aqueous mixture comprising a t...  
WO/2009/068534A1
The present invention relates to a method for preparing a salt of trifluoromethanesulphinic acid termed "triflinic acid". More specifically, the invention relates to a method for preparing a highly pure triflinic acid salt. The method of...  
WO/2009/039181A3
Organocatalysts, particularly proline sulfonamide organocatalysts, having a first general formula as follows are disclosed. Embodiments of a method for using these organocatalysts also are disclosed. The method comprises providing a disc...  
WO/2009/009041A3
The invention relates to compounds and methods for modulating one or more components of a kinase cascade.  
WO/2009/009041A2
The invention relates to compounds and methods for modulating one or more components of a kinase cascade.  
WO/2008/110698A3
The invention relates to a method for preparing polyfluorinated sulphanylamides of formula (I) and polyfluorinated sulphinamidines of formula (II), wherein R1-R4 are defined as in the claims, and for preparing the precursors of same.  

Matches 1 - 50 out of 8,753