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Matches 601 - 650 out of 4,313

Document Document Title
WO/1992/013872A1
Compounds of general formula (I) in the form of a 22R and 22S epimer, wherein X1 and X2 are the same or different and each represents a hydrogen atom or a fluorine atom, provided that X1 and X2 are not simultaneously a hydrogen atom, pro...  
WO/1992/013823A1
A compound of formula (I), or a salt or solvate thereof, in which R1 and R2 each independently represents hydrogen, alkyl, optionally substituted aryl or optionally substituted aralkyl; R3 represents alkyl, optionally substituted aryl or...  
WO/1992/012152A1
Azabicyclo[2.2.2]octan-3-imines of general formula (I), wherein R1, R2 and R3 are as defined herein are prepared by reacting a compound of formula (II) with a compound of formula (III), wherein A is MgCl, MgBr or Li.  
WO/1992/012180A1
Novel cyclodextrin and epichlorohydrin based polymers are obtained by adding an epoxy-ammonium salt to a cyclodextrin-epichlorohydrin polycondensate wherein the ratio of cyclodextrin to epichlorohydrin is 1:3 to 1:10 and the proportion o...  
WO/1992/012135A1
Optically substantially pure (-) enantiomer of [[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl] hydrazono]propanedinitrile or pharmaceutically acceptable salt thereof, intermediates and a process for the preparation are descr...  
WO/1992/008702A1
A method for resolving chiral hydantoins having general formula (I), wherein R1 is a lower alkyl radical having 1-5 carbon atoms in a linear or branched chain; and R2 is a phenyl radical which is optionally mono-, di- or trisubstituted b...  
WO/1992/005151A1
This invention relates to salts of formula (I) where, A is 1 and X is 1 or 2; R1 is C8 to C13 alkyl, C7 to C12 alkoxy, C7 to C12 alkylthio, C10 to C12 1-alkynyl, 10-undecynyloxy, 11-dodecynyl, phenyl-C4 to C10 alkyl, phenyl-C3 to C9 alko...  
WO/1992/003404A1
Process for transforming (benzoyl-3 phenyl)-2 propionic-R(-) acid into an S(+) isomer through the action of a base either in situ during the splitting of racemic ketoprofen or on the crystallization mother liquor of a (benzoyl-3 phenyl)-...  
WO/1992/002283A1
The media is an ether derivative of cyclodextrin such as a permethylated hydroxy ether of cyclodextrin or a dialkyl trifluoroacetyl ether derivative of cyclodextrin and is used in capillary gas chromatographic columns. Particular benefit...  
WO/1992/000965A1
1R-cis,1'R-cis isomer of a 2',2'-(3,11-dioxo-4,10-dioxatridecylene)-bis-(1,2,3,4-tetrah ydro-6,7-dimethoxy-2-methyl-1-veratrylisoquinolinium) salt, substantially free from other geometrical and optical isomers thereof. The 1R-cis,1'R-cis...  
WO/1992/000275A1
The description relates to a process for producing enantiomer-pure $g(a)-hydroxypropionoaldehyde derivatives of the general formula (I) in which: R¿1? is the substituent Q which may be a hydrocarbon radical interrupted by oxygen atoms, ...  
WO/1991/018878A1
Novel processes are disclosed for the preparation and resolution of substituted piperidines of formula (I), wherein R1 and R2 are defined as below, and related compounds, as well as novel intermediates used in such processes.  
WO/1991/018910A1
A compound of general formula (I), in which each of R1, R2, R3 and R4 independently represent a hydrogen atom or a group -(CO)nR5 in which n is 0 or 1 and R5 represents an alkyl, aryl, cycloalkyl, alkaryl or aralkyl group, or R1 or R2 to...  
WO/1991/017816A1
The invention relates to a process for the high yield, cost efficient means of separating enantiomers. The process utilizes a supported liquid membrane and a chiral carrier which selectively complexes with one of the two enantiomeric opt...  
WO/1991/017977A1
Process for the stereoselective preparation of phenylisoserin derivatives of general formula (I) from benzylamine. In the general formula (I), R is a phenyl radical or tert.butoxy and R1 is a hydroxy function protective group.  
WO/1991/017159A1
(-)-4-Amino-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyr imidin-2-one, its pharmaceutically acceptable derivatives, pharmaceutical formulations thereof, methods for its preparation and its use as an antiviral agent are described.  
WO/1991/015471A1
A process is disclosed for the isolation of an enantiomerically enriched alcohol from a first mixture of an enantiomerically enriched alcohol and an enantiomerically enriched ester. The process includes the steps of: (a) contacting the m...  
WO1991013066A3  
WO/1991/015472A1
A process is disclosed for the separation of an enantiomerically enriched 1-tosyloxy-2-acyloxy-3-butene and an enantiomerically enriched 1-tosyloxy-2-hydroxy-3-butene from a first mixture containing both compounds. The process includes t...  
WO/1991/014671A1
The new (S)-4-(2-bromobenzoyl)-5-hydroxy-benzocyclobutene-1-carboxyl ic acid, i.e., the compound of formula (I), in free or salt form, can be used as the active substance in pharmaceutical preparations and can be made by a new process wh...  
WO/1991/013066A2
Method for the preparation of beta-phenylglycidic-(2R,3R) acid optionally in the form of salt or ester by precipitation of the salt of the beta-phenylglycidic-(2R,3R) acid with (+)-alpha-methylbenzylamine-(R) in a solution of a mixture o...  
WO/1991/013046A1
A process for separating optical isomers in a pseudo-moving bed system, which comprises introducing a solution containing an optical isomer mixture and a desorbing liquid into a packed bed containing an optical resolution packing therein...  
WO/1991/012072A1
Disclosed are processes and apparatus for separating a desired solute (A), such as an optically active isomer, from a complex mixture (A, X, Y) using carrier (C) facilitated transport in an immobilized liquid membrane (50) or carrier (C)...  
WO/1991/007366A1
A novel process for preparing the R(+)-enantiomer of terodiline (N-tert.butyl-1-methyl-3,3-diphenylpropylamine) and pharmaceutically acceptable salts thereof by optical resolution of a racemic mixture of terodiline using tartaric acid, c...  
WO/1991/002006A1
New polysaccharide derivatives useful for the separation of optical isomers, prepared by substituting at least one atomic group of formula (1), (2) or (3) for part or the whole of hydrogen atoms of the hydroxyl or amino groups of the pol...  
WO/1991/000270A1
The invention relates to a novel process for the resolution of an acid mixture (hereinafter: threo acid mixture) containing (+)-threo-3-[(2-aminophenyl)thio]-2-hydroxy-3-(4-methoxyphen yl)propionic acid [hereinafter: (+)-threo acid] and ...  
WO/1990/009376A1
A process for the optical resolution of racemic 1,4-dihydropyridines, containing isothioureido groups. Salification of racemic isothioureas with optically active acids produces diasteroisomeric mixtures of isothiouronium salts, that, usi...  
WO/1990/008126A1
The invention relates to a novel process for preparing the optical isomers of 2,2-dimethyl-3-(2,2-disubstituted vinyl)cyclopropanecarboxylic acids of general formula (I), wherein R1 and R2, independently from another, stand for halogen o...  
WO/1990/003962A1
A novel process for the preparation of compounds of formula (I), wherein X is -CH2CH2- or -CH=CH-; R1 is an ester group inert to the reaction conditions; and R is an organic radical having groups which are inert under reducing conditions...  
WO/1989/009235A1
Substituted cylodextrins of general formula (I), where R2 and R6 are linear-chain or branched-chain alkyl or alkenyl groups with 1 to 8 atoms of carbon or cycloalkyl groups with 5 to 8 atoms of carbon, which can be equal or different, an...  
WO/1988/010249A1
Crystallizable pyrethroid isomer or enantiomer pairs are converted to more pesticidally active isomers by contacting a hydrocarbon slurry of the starting isomers with a base and a catalyst, the catalyst being substantially soluble in the...  
WO/1988/007050A1
Process for the production of (+)-bicyclo-[3.3.0]octane-3-on-2-carboxylic acid steroid esters having the formula (I), in which X represents oxygen or the -O-(CH2)n-O- or the -O-CH2-C(CH3)2-CH2-O- residue; n represents 2 or 3; R2 represen...  
WO/1988/001614A1
A process for the resolution of dl-methyl 3-[4-(2-hydroxy-3-isopropylamino)propoxy]phenylpropionate [(dl-esmolol)] into a dextro (+) and a levo (-) isomer.  
WO/1987/006929A1
A new chiral reagent of formula (I), wherein X is halogen, an azide group or a succinimidyl group and wherein R is an alkyl group or a trifluormethyl group. The invention further relates to a method for derivatization, determination and ...  
WO/1987/000165A1
The system comprises two immiscible liquid phases and one or more enantioselectively binding chiral components, each of which is substantially in one of said phases. Also disclosed is a method for chiral resolution of racemic mixtures, o...  
WO/1986/004215A1
An insecticidal composition containing more than one active ingredients which comprises as active ingredient in an amount of 0.001-99% by weight a synthetic pyrethroide of general Formula (I), (wherein X stands for chlorine or bromine) -...  
WO/1986/004216A1
A synergistic insecticidal composition containing more than one active ingredients and being harmless to environment characterized by comprising in an amount of from 0.001 to 99% by weight a synthetic pyrethroide of the formula (I) - nam...  
WO/1986/001799A1
A novel sequence of highly selective chemical reactions for conversion of 3-Aryl-2-propyn-1-ols into cis-1-Aryl-3-fluoro-1-propene and into D,L-(threo)-1-Aryl-2-acylamido-3-fluoro-1-propanols. Preparation of D-(threo)-1-Aryl-2-acylamido-...  
WO/1986/000066A1
New butyramide derivatives corresponding to formula (I), wherein X and Y independently represent hydroxymethyl; cyano; carboxy; functionally modified carboxy selected from esterified carboxy, carbamoyl, and N-substituted carbamoyl; 5-tet...  
WO/1985/003932A1
The separation of optically active phenylalanine and N-acyl derivatives thereof and novel diastereomer salts of the said compounds. According to the invention a racemic compound of formula (I), is reacted with an optically active resolvi...  
WO/1985/000661A1
A packing for use in liquid chromatography for optical resolution of racemic compounds, which comprises a carrier of silica gel having bound thereto a spacer introduced by reacting with a silane treating agent and having chemically bound...  
WO/1983/004103A1
A grafted chromatographic filler comprising an inorganic carrier having hydroxy groups on its surface to which alpha-arylalkylamine derivative is grafted, said alpha-arylalkylamine derivative comprising asymmetric carbon-containing, opti...  
JPWO2018212216A1
A manufacturing method of an optically active substance including an asymmetric induction process of raising an abundance ratio of one Enantiomer of the chiral molecule is provided by making an asymmetric induction agent act on a chiral ...  
JP2020040957A
[Subject] Offer of a method of preparing a new Kinazo linon derivative which checks PI3K (phosphatidyl inositol 3-kinase), and a derivative, and a medicine constituent containing the Kinazo linon derivative which treats a blood new organ...  
JP2020506160A
The simple preparing method of red-throated loon Bactam is provided, and let piperidine 5-on- 2S-formate ester II be materials, After carrying out a condensation reaction to the hydroxylamine hydrochloride which has a О-blocking group, ...  
JP2020500158A
The present invention is a repeat unit of formula (RR)-(IA), formula (SS)-(IA), formula (RS)-(IA), or formula (SR)-(IA), Or it is related with the constituent containing a crystalline metal organicity structure and it including the repea...  
JP2019218402A
To provide a method for producing an optically active valeric acid derivative substituted with a cycloalkyl group with high purity.A method of producing a high-purity compound represented by formula (5) comprises adding (S)-2-amino-1-pro...  
JP2019531307A
The present invention relates to a method of condensing mirror image isomer from a mirror image isomer mixture by judgment fusion crystallization within a fusion crystallizing device. Especially the present invention relates to chiral Te...  
JP2019530709A
1R, (R [3]) -, or 1S and (3S) - Enantiomer of 2 and 2-dichloro 3- (substitution phenyl) cyclopropane carboxylic acid, It is manufactured by the method of following processing by the acid of the above-mentioned salt on isolation and the l...  
JP2019530723A
The compound denoted by formula (I) applicable as hepatitis C virus inhibitor of the present invention or its optical isomer, the salt permitted pharmacologically, a hydrate, or solvent Japanese food , It can apply to the medical treatme...  

Matches 601 - 650 out of 4,313