Login| Sign Up| Help| Contact|

Patent Searching and Data


Matches 151 - 200 out of 31,007

Document Document Title
WO/2017/004349A2
The present invention provides methods for the production of terephthalic acid and derivatives thereof using ethylene oxide, carbon monoxide and furan as feedstocks. The process is characterized by high yields and high carbon efficiency....  
WO/2016/207025A1
Described is a method that involves synthesizing a mixture containing 5-hydroxmethylfurfural (HMF, compound of formula (I)), and separating 5-hydroxymethylfurfural from the obtained mixture. The disclosed method involves step (A), synthe...  
WO/2016/208862A1
The present invention provides: a compound which can implement the low driving voltage, high light-emitting efficiency and high heat resistance of an element, and improve the color purity and lifespan of the element; an organic electric ...  
WO/2016/207365A1
The invention relates to a method for continuously producing 5-hydroxymethylfurfural (referred to as HMF below, a compound of the formula (I)) in a reactor arrangement, having the following steps: - setting reaction conditions in a mixtu...  
WO/2016/207217A1
Compounds of formula (I); wherein R1, R2, R3, R4, R5, R6, R7, R8, R14, W, A and n are as defined in the description. Medicaments.  
WO/2016/206909A1
The present invention relates to a process for preparing 5-hydroxymethylfurfural (also referred to hereinafter as "HMF", compound of the formula (I)) and humins, comprising steps (a), (b), (c), (d), (e) and (f) (cf. figure 1 and the appe...  
WO/2016/205202A1
The present disclosure provides treprostinil derivatives that can act as prodrugs of treprostinil. The treprostinil derivatives can be used to treat any conditions responsive to treatment with treprostinil, including pulmonary hypertensi...  
WO/2016/205539A1
Disclosed herein are methods of inducing sperm deformation. In certain embodiments, the method includes contacting a sperm with an effective amount of triptonide, thereby inhibiting sperm motility. Also disclosed herein are methods of co...  
WO/2016/202965A1
The present invention relates to a novel method for preparing pantolactone by reacting hydroxypivalaldehyde cyanohydrin in a phase separation method.  
WO/2016/203402A1
The design and synthesis of a novel bis-furan scaffold tailored for high efficiency at inhibiting transthyretin amyloid formation is reported. In vitro results show that the discovered compounds are more efficient inhibitors of amyloid f...  
WO/2016/199784A1
A compound represented by formula (1) is a material which enables the achievement of an organic electroluminescent element having a long service life and being able to be driven at a low voltage. (In formula (1), R1-R4, a-d, L0-L2 and Ar...  
WO/2016/199906A1
The purpose of the present invention is to provide a novel low-molecular-weight compound which exhibits orexin receptor agonist activity and is expected to be useful as a prophylactic agent or therapeutic agent for narcolepsy and the lik...  
WO/2016/199172A3
The present invention disclosed a novel compound of formula (I), (II) and (III) and process for preparation thereof. Further, the present invention provides a pharmaceutical composition comprising compound of formula (I) or (II) or (III)...  
WO/2016/198507A1
Compound of formula (I) wherein A is selected from (i), where RF1 is H or F; (ii); (iii) a N-containing C6 heteroaryl group; and B is (B), where X1 is either CRF2 or N, where RF2 is H or F; X2 is either CR3 or N, where R3 is selected fro...  
WO/2016/199743A1
The present invention provides an arylamine compound represented by general formula (1). The arylamine compound according to the present invention is a novel compound, and has higher hole mobility than conventional hole transport materia...  
WO/2016/198374A1
Substituted aromatic sulfonamides of formula (I) pharmaceutical compositions and combinations comprising said compounds and the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a di...  
WO/2016/197398A1
Disclosed are a sulfonic acid inner salt compound of amidine and a preparation method therefor. The product of a sulfonic acid inner salt of amidine is obtained and synthesized by adopting an o-aminobenzenesulfonyl chloride compound and ...  
WO/2016/198744A1
The invention relates to a method and an apparatus for producing a chemical compound from biomass based raw material. According to the invention, the biomass based raw material (1) is gasified in a gasification device (2) for forming a g...  
WO/2016/199789A1
The present invention addresses the problem of efficiently synthesizing a trifluoromethyl substituted semisquarate in a short process, in order to manufacture trifluoromethyl compounds with various functionalities. A method was developed...  
WO/2016/194901A1
Provided is a method for producing furfural, which enables furfural to be produced at higher yields from biomass starting materials containing hemicellulose. In this method for producing furfural, after contacting the biomass starting ma...  
WO/2016/191872A1
Methods and compositions are provided for the treatment of familial exudative vitreoretinopathy (FEVR) through the administration of a therapeutically effective amount of a sphingosine-1-phosphate receptor type 2 (S1PR2) antagonist. Also...  
WO/2016/195499A1
A purified acid composition comprising 2,5-furandicarboxylic acid is prepared by a process comprising a) providing an acid composition solution of a crude acid composition in a polar solvent, the crude acid composition comprising 2,5-fur...  
WO/2016/195077A1
This novel guanidine compound having excellent bactericidal activity is represented by formula [I]. (In the formula, Y represents a divalent group represented by formula [II] (wherein each of R7-R9 independently represents a hydrogen ato...  
WO/2016/195115A1
A supported catalyst for aldehyde coupling reaction, comprising a carrier having supported thereon a catalyst comprising at least one azolium compound selected from the group consisting of a thiazolium salt, an imidazolium salt, a benzim...  
WO/2016/195361A1
The present invention provides: a novel benzylidene dihydroindenone derivative; and a composition for preventing or treating inflammatory bowel disease, containing the same. The benzylidene dihydroindenone derivative maintains the thickn...  
WO/2016/193822A1
A process for preparing (E)-(5,6-dihydro-l,4,2-dioxazin-3-yl)(2- hydroxyphenyl)methanone O-methyl oxime is described which includes: (i) reacting benzofuran-3(2H)-one O-methyl oxime (1) with at least one nitrite selected from n-butyl nit...  
WO/2016/193459A1
The present invention relates to compounds according to Formula I: or a pharmaceutically acceptable salt thereof. The compounds can be used as inhibitors of RORy and are useful for the treatment of RORy mediated diseases such as autoimmu...  
WO/2016/192631A1
The present invention provides an abietane-type diterpene compound having lipid-lowering activity, a method for preparing same, and use of same. Specifically, the compound has the structure shown in formula I. The definitions of the grou...  
WO/2016/193332A1
Ether analogues of galiellalactone, methods of preparing the analogues, and use of the analogues in the treatment of cancer are disclosed.The analogues are of formula (I) or (II):  
WO/2016/195500A1
A purified acid composition comprising 2,5-furandicarboxylic acid is prepared in a process, comprising (i) oxidizing a feedstock containing 5-alkoxymethylfurfural to an oxidation product comprising 2,5-furandicarboxylic acid (FDCA) and 2...  
WO/2016/189876A1
The present invention provides a urea derivative or a pharmacologically acceptable salt thereof that has a formyl peptide receptor like 1 (hereinafter may be abbreviated as FPRL1) agonist effect, a pharmaceutical composition containing t...  
WO/2016/189877A1
The present invention provides a urea compound or a pharmacologically acceptable salt thereof that has a formyl peptide receptor like 1 (hereinafter may be abbreviated as FPRL1) agonist effect, a pharmaceutical composition containing the...  
WO/2016/191682A1
Acid chloride derivatives of 5-(chloromethyl)furan-2-carboxylic acid and furan-2,5-dicarboxylic acid (FDCA) can be produced in high yield by treatment of the precursor aldehydes 5-(chloromethyl)furfural (CMF) and 2,5-diformylfuran (DFF) ...  
WO/2016/190739A1
A fructose-rich solution is prepared from a solid composition comprising fructose and glucose, in a process comprising i) admixing the solid composition comprising fructose and glucose with a selective solvent that consist for at least 8...  
WO/2016/190170A1
A polyimide, which is produced from a tetracarboxylic acid dianhydride represented by formula (1) and having both a cyclic hydrocarbon skeleton and an ester group, has excellent solubility in solvents, excellently low dielectric properti...  
WO/2016/190600A1
The present invention provides a compound represented by chemical formula 1. Further, the present invention provides an organic electric element comprising a first electrode, a second electrode, and an organic matter layer between the fi...  
WO/2016/186276A1
The present invention relates to an organic compound represented by chemical formula 1, an organic optoelectronic element, and a display device.  
WO/2016/186278A1
The present invention relates to a method for preparing 2,5-furandicarboxylic acid (FDCA), the method comprising oxidizing 5-hydroxymethylfurfural (HMF) in a mixture solvent containing an alcohol and an organic acid, in the presence of a...  
WO/2016/186505A1
A carboxylic acid-containing composition, which composition contains an aldehyde, is purified in a process, which process comprises introducing the carboxylic acid-containing composition and an aqueous electrolyte into an electrolytic ce...  
WO/2016/186504A1
An aromatic dicarboxylic acid of chemical formula HOOC-Ar1-COOH is prepared in a process wherein a feedstock comprising at least an aromatic aldehyde compound of chemical formula (1): OHC-Ar1-COOH, wherein Ar1 represents an arylene or he...  
WO/2016/186963A1
The present invention provides a compound having the structure : Formula (I).  
WO/2016/181413A1
The present invention relates to an enantiospecific process for the preparation of (R) and (S) enantiomers of sex pheromones of the long-tailed mealybug with high enantiopurity.  
WO/2016/181413A4
The present invention relates to an enantiospecific process for the preparation of (R) and (S) enantiomers of sex pheromones of the long-tailed mealybug with high enantiopurity.  
WO/2016/178544A2
The present invention relates to a novel compound and, more particularly, to a novel compound which forms a deep HOMO, has a high LUMO enabling easy electron blocking, and has an excellent hole mobility, thereby suppressing a roll-off ph...  
WO/2016/178544A3
The present invention relates to a novel compound and, more particularly, to a novel compound which forms a deep HOMO, has a high LUMO enabling easy electron blocking, and has an excellent hole mobility, thereby suppressing a roll-off ph...  
WO/2016/176082A1
Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, wherein R1, R2, R3, R4, R5, Q1, Q2, Y1, and Y2 are as defined in the disclosure. Also disclosed are compositions containing the compounds of ...  
WO/2016/175533A2
The purpose of the present invention is to provide: a compound having a high light emitting efficiency, a low driving voltage, and an improved lifespan of an element; an organic electronic element using the same; and an electronic device...  
WO/2016/175533A3
The purpose of the present invention is to provide: a compound having a high light emitting efficiency, a low driving voltage, and an improved lifespan of an element; an organic electronic element using the same; and an electronic device...  
WO/2016/173274A1
Aromatic farnesyl compound and application of a pharmaceutical salt thereof as an inhibitor of α-glucosidase, dipeptidyl peptidase-4, aldose reductase, protein tyrosine phosphatase-1B or HMG-CoA reductase, or use thereof in preparing me...  
WO/2016/168938A1
Described herein is an antibiotic compound of formula (I): or a salt or stereoisomer thereof; wherein R1-R3, R5 and R6 are independently selected from H, alkyl group, substituted alkyl group, halogen, OH, NH2, or SH; R4 is H, alkyl group...  

Matches 151 - 200 out of 31,007