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Matches 651 - 700 out of 29,396

Document Document Title
WO/2013/130958A1
The present invention relates to novel benzofuran-2-sulfonamide derivatives formula (I), processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals as modulators of chemokine receptors.  
WO/2013/125211A1
The purpose of the present invention is to provide an optical film that produces a large amount of in-plane retardation and sufficient reverse wavelength dispersion even with a low film thickness. This optical film contains a thermoplast...  
WO/2013/124745A9
The invention relates to a novel process for the preparation of dronedarone (I) and pharmaceutically acceptable salts thereof (formula I), which comprises oxidizing a compound of formula (VI), or a salt thereof and the obtained product i...  
WO/2013/124745A1
The invention relates to a novel process for the preparation of dronedarone (I) and pharmaceutically acceptable salts thereof (formula I), which comprises oxidizing a compound of formula (VI), or a salt thereof and the obtained product i...  
WO/2013/125599A1
[Problem] To provide an organic compound which is easy to synthesize and has excellent chemical stability, semiconducting properties (high carrier mobility) and high solubility in a solvent. [Solution] A compound represented by formula (...  
WO/2013/125732A1
The present invention provides a compound having a GOAT inhibitory action, which is useful for the prophylaxis or treatment of obesity and the like, and has superior efficacy. The present invention is a compound represented by the formul...  
WO/2013/121209A1
A compound of formula I, and its pharmaceutically acceptable salt or salts and physiologically hydrolysable derivatives in free form or salt form: (Formula (I)) wherein either Q1, CR6a and optionally R6b together form a cyclic moiety whe...  
WO/2013/121235A3
The invention relates to a process for preparation of dronedarone of formula (I) and pharmaceutically acceptable salts thereof characterized in that from the compound of formula (II). the hydroxyl group is removed,. and the obtained prod...  
WO/2013/122905A1
A method of making acid anhydrides from epoxide and carbon monoxide feedstocks is presented. In various aspects, the method includes steps of reacting the contents of a feed stream comprising an epoxide, a solvent, a carbonylation cataly...  
WO/2013/121235A2
The invention relates to a novel process for preparation of dronedarone of formula (I) and pharmaceutically acceptable salts thereof the hydroxyl group is removed, and the obtained product is isolated and, if desired, converted into a ph...  
WO/2013/121234A1
The invention relates to a novel process for the preparation of dronedarone (I) and pharmaceutically acceptable salts thereof which comprises oxidizing a compound of formula (IV) or a salt thereof with an oxidizing agent in an organic or...  
WO/2013/120229A1
Disclosed is a method for preparing aqueous nanoparticle suspensions of derivatives of 4,9-dihydroxy-naphtho[2,3-b]furan aliphatic acid esters. The compositions and the uses of the aqueous nanoparticle suspensions prepared according to t...  
WO/2013/120876A1
The present invention pertains to novel enaminoketones containing a CF3O-group, novel pyrazole-derivatives containing a CF3O group as well as to a novel process for their preparation comprising aminoformylation of CF30-ketones and cycliz...  
WO/2013/118847A1
An organic EL element with high efficiency and long life, an electronic device mounting said element, and compound making it possible to provide such an organic electroluminescent element are provided. Said compound is specifically repre...  
WO/2013/117585A1
Disclosed is a method for obtaining furan derivatives from D-glucose. In said method, A) D-glucose is transformed into D-fructose in an enzymatic process in which redox cofactors are used and regenerated, one of the two redox cofactors b...  
WO/2013/118907A1
An amide compound represented by formula (I) has an excellent pest control effect. (In the formula, Y represents a 3-7 membered saturated heterocyclic ring which contains, as ring-forming component(s), one or more atoms or groups that ar...  
WO/2013/118905A1
An amide compound represented by formula (I) has an excellent pest control effect. (In the formula, Y represents a 3-7 membered saturated heterocyclic ring which contains, as ring-forming component(s), one or more atoms or groups that ar...  
WO/2013/117120A1
Provided in the present invention are a 2-arylbenzofuran-7-formamide compound as shown in general formula I or a pharmacologically or physiologically acceptable salt thereof, a preparation method thereof and use thereof in preparing anti...  
WO/2013/115378A1
The present invention relates to: a method for producing a ruthenium catalyst, wherein ruthenium supported by a metal oxide is pretreated with an aldehyde compound, a phosphorus compound and a lower alcohol compound; and a method for pro...  
WO/2013/114040A1
The present invention relates to novel organic compounds, to the process for synthesizing same and to the uses thereof, in particular in the field of cancer treatment. In particular, the present invention relates to novel anticancer comp...  
WO/2013/110313A1
Compounds of formula (I) are provided wherein R1 represents H, CN and CF3; R2 represents 1-naphthyl, 3,5-dichlorophenyl, 4-(4-fluorophenylthio)phenyl or phenyl substituted with one or more substituent selected from halogen, methoxy, cyan...  
WO/2013/107904A1
The invention relates to an alkoxycarbonylation process for the preparation of an optionally substituted alkanoic acid ester comprising reacting: (a) an optionally substituted alkene or a mixture thereof; (b) a source of a group 8-10 met...  
WO/2013/107947A1
The present invention describes a method for pretreating lignocellulosic biomass comprising: a) a step of acid hydrolysis of the biomass with an acid solution resulting in a liquid fraction and a solid fraction, b) a step of separating t...  
WO/2013/107948A1
The present invention relates to a method for preprocessing lignocellulosic biomass, include: a) a step for the acid hydrolysis of the biomass using an acid solution so as to obtain a liquid fraction and a solid fraction; a step of separ...  
WO/2013/109477A1
Processes are disclosed for the conversion of a carbohydrate source to hexamethylenediamine (HMDA) and to intermediates useful for the production of hexamethylenediamine and other industrial chemicals. HMDA is produced by direct reductio...  
WO/2013/104257A1
Disclosed in the present invention are polycyclic derivatives as represented by general formula (I), the preparation method thereof, pharmaceutical compositions containing the derivatives and uses thereof as therapeutical agents, especia...  
WO/2013/105708A1
The present invention relates to a method for preparing α-metylene lactone comprising the steps of: (A) preparing an enolate intermediate by reacting lactone with alkyl formate under conditions in which an alcoxide base exists; and (B) ...  
WO/2013/105118A1
Disclosed herein is a novel route of synthesis of syn azide epoxide of formu 5, which is used as a common intermdeiate for asymmetric synthesis of HIV protease inhibitors such as Amprenavir, Fosamprenavir, Saquinavir and formal synthesis...  
WO/2013/106136A1
Hydroxymethylfurfural is made from an aqueous hexose sugar solution, especially from a high fructose corn syrup product. By rapidly heating the sugar solution to the elevated temperatures involved as well as rapidly cooling the resultant...  
WO/2013/106137A1
A process is described wherein a feed of a six-carbon carbohydrate-containing material or of a furanic dehydration product from a six-carbon carbohydrate-containing material or of a combination of these is supplied to a reactor in a cont...  
WO/2013/105118A8
Disclosed herein is a novel route of synthesis of syn azide epoxide of formu 5, which is used as a common intermdeiate for asymmetric synthesis of HIV protease inhibitors such as Amprenavir, Fosamprenavir, Saquinavir and formal synthesis...  
WO/2013/102935A2
The present invention disclosed herein is a novel commercially feasible, one pot synthesis of library of 3-substituted phthalides of formula I via CuCN mediated oxidative cyclization in high yield. Formula I  
WO/2013/102911A1
The present invention relates to a process for chemical conversion of cellulose isolated from aromatic spent biomass to hydroxymethyl furfural using an eco-friendly and economical liquids system with recoverable and reusable solid Indion...  
WO/2013/102935A3
The present invention disclosed herein is a novel commercially feasible, one pot synthesis of library of 3-substituted phthalides of formula I via CuCN mediated oxidative cyclization in high yield. Formula I  
WO/2013/097042A1
Disclosed is a compound of formula 1, as shown below, where R1, R2, R3, R4, R5, R6 and R7 are as described herein. Also, disclosed is a process for the preparation of compounds of formula 1, and intermediates used therein. The compound o...  
WO/2013/100467A1
The present invention relates to a compound for an organic optoelectric device, an organic light-emitting diode including the same, and a display device including the organic light-emitting diode, wherein the compound for the organic opt...  
WO/2013/099998A1
The present invention is a radiation-sensitive resin composition which contains [A] a polymer that has a structural unit represented by formula (1) and [B] an acid generator. In formula (1), R2 represents a hydrogen atom or a monovalent ...  
WO/2013/100464A1
The present invention relates to a compound for an organic optoelectronic element, to an organic light-emitting element comprising same and to a display device comprising the organic light-emitting element; and provided is a compound for...  
WO/2013/101970A1
Disclosed are processes comprising contacting an aqueous reaction mixture having an initial pH between about 3 and about 6 and comprising levoglucosenone with a catalyst, and heating the reaction mixture to form a product mixture compris...  
WO/2013/102000A1
Furfural is produced by contacting an aqueous feedstock solution containing C5 sugar and/or C6 sugar using a soluble acid catalyst with reactive distillation. Both high yield and high conversion are obtained in the reaction vessel. Degra...  
WO/2013/101977A1
Disclosed herein are processes comprising contacting isosorbide with hydrogen in the presence of a first hydrogenation catalyst to form a first product mixture comprising tetrahydrofuran-2, 5-dimethanol. The processes can further compris...  
WO/2013/102015A1
Furfural is produced by contacting a feedstock solution containing C5 sugar and/or C6 sugar with a solid acid catalyst using reactive distillation. Both high yield and high conversion are obtained, without production of insoluble char in...  
WO/2013/096998A1
The present invention refers to a process for production of a mix¬ ture comprising 2,4-furandicarboxyiic acid (2,4-FDCA) and 2,5 furandicar- boxyiic acid (2,5-FDCA) through the disproportionation route, using as base compounds oxidation...  
WO/2013/097752A1
Disclosed are natural products as retinoic acid receptor (RARs) excitomotors and the uses thereof. The marine natural products Luffariellolide and Manoalide are specific excitomotors of retinoic acid receptors (RARs), able to inhibit the...  
WO/2013/099553A1
Provided is a novel 2-fluorophenylpropionic acid derivative which has excellent anti-inflammatory/analgesic effects, while avoiding side effects such as gastrointestinal disorders, namely a 2-fluorophenylpropionic acid derivative represe...  
WO/2013/098416A2
The present invention relates to the use of compounds for the treatment or prevention of pain in mammals, in particularly in human beings, and also to a process for preparing these compounds.  
WO/2013/102027A1
Furfural is produced by mixing an aqueous feedstock solution containing C5 sugar and/or C6 sugar with a heated high boiling, water-miscible solvent, such as sulfolane, and a solid acid catalyst. Furfural product and water can be distille...  
WO/2013/102002A1
Processes for making furfural and 5-hydroxymethylfurfural from sugars are provided. The processes can be carried out using a batch process or a continuous mode of operation. An aqueous sugar solution is pressurized with CO2, thereby prod...  
WO/2013/097773A1
The invention provides novel ethylene derivatives represented by Formula I, which may be used as selective estrogen receptor modulators (SERMs) and useful in the prophylaxis and/or treatment of estrogen-dependent conditions or conditions.  
WO/2013/098416A3
The present invention relates to the use of compounds for the treatment or prevention of pain in mammals, in particularly in human beings, and also to a process for preparing these compounds.  

Matches 651 - 700 out of 29,396