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Matches 1,001 - 1,050 out of 4,297

Document Document Title
JP2012001525A
To provide a method for producing highly pure optically active trans-4-fluoroproline.In the method for producing the optically active trans-4-fluoroproline, when hydrogeneration reaction and deprotection reaction of a protection group of...  
JP2011530504A
therapeutic method Seki of a CNS disease and pathology where the non-racemic mixture of ロフェキシジンエナンチオマー was used for the present invention -- it carries out. The present invention relates to the manufacturing m...  
JP4842819B2  
JP4843615B2  
JP4834333B2  
JP4836897B2  
JP2011529469A
The present invention discloses a process for isolating enantiomer components from a mixture of enantiomers through particle-size-controlled crystallization, comprising the steps of: (a) forming a solution of a mixture of enantiomers (R)...  
JP2011241191A
To provide a method for producing an optically active alcohol in high yield with high enantio-selectivity from a ketone compound.The method for producing an optically active alcohol includes a step of allowing a ketone compound to react ...  
JP4825825B2  
JP2011528671A
Disclosed is a process for preparing chiral pharmaceutical intermediates of R-beta-amino phenylbutyric acid derivatives (I) and pharmaceutically acceptable salts thereof, which affords the desired object compounds having special optical ...  
JP2011236157A
To provide a method for producing an optically active 3-aminopiperidine derivative important as the raw material for medicine using inexpensive, easily obtainable raw material by an industrially suitable method.The method for producing o...  
JP2011236251A
To provide a new crystalline polymorphic form of substantially optically pure (-)-[[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phe nyl]hydrazono]propanedinitrile.There is provided the crystalline polymorphic form I of (-)-[[4-(1,...  
JP2011231071A
To provide an industrial optical resolution which obtains optical activity (R)-1-(4-fluoro phenyl)ethylamine.The optical resolution is carried out using natural type L-(-)-malic acid as a resolving agent, thereby optical activity (R)-1-(...  
JP4816454B2  
JP4812434B2  
JP2011219419A
To provide a triazole compound exhibiting remarkably excellent noxious organism-controlling activity and to provide (+)-1-[2,4-dimethyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl]- 3-(trifluoromethyl)-1H-1,2,4-triazole.The optically active (...  
JP4800213B2  
JP4797251B2  
JP2011526614A
A method including making S* of 2* arylpropionic acid compound or R* mirror image isomer which manufactures a racemic 2* arylpropionic acid compound or its salt in which permission on pharmacy is possible, and which is a method and corre...  
JP4790128B2  
JP4787795B2  
JPWO2009142194A
An amino alcohol derivative is obtained with high optical purity, and it develops that it is cheap and there is a manufacturing method compoundable extensive. For example, a general formula,Inside of a formula, R1は, for example, a trih...  
JP4783496B2  
JP4780536B2  
JP2011183361A
To provide a new separator usable as a separator for chromatography and carrying a cyclic oligosaccharide.The separator is prepared by carrying on a carrier the cyclic oligosaccharide comprised of a repeating unit of a D-glucopyranoside ...  
JP4776846B2  
JP4778178B2  
JP2011524909A
The present invention aims at the synthesizing method of practical quantity 収率 for preparing the compound of general formula III, IV, V, VII, VIII, IX, X, XII, XIV, and XV. Such a compound can be changed in order to prepare the outpu...  
JP2011524907A
The medicine constituent containing out the crystal R (+) *N* propargyl *l* amino in and this containing the water of less than 0.5% of the weight of quantity, manufacturing method, and verification are indicated. The preparing method of...  
JP4768145B2  
JP4769562B2  
JP4768638B2  
JP4768953B2  
JP4761769B2  
JP4763771B2  
JP4754753B2  
JP4752285B2  
JP4750265B2  
JP4747320B2  
JP4745655B2  
JP2011522023A
The present invention relates to an improved process for the preparation of (R)-1-aminoindan (2), rasagiline (1) and pharmaceutically acceptable salts of rasagiline.  
JP2011144162A
To provide a new crystal of an optically active 4-amino-3-(4-chlorophenyl)butanoic acid, and a method for producing the same.This method for producing the following crystal A, comprising a process of heating the following crystal B in wa...  
JP4735263B2  
JP4728548B2  
JP4728636B2  
JP4723245B2  
JP4719471B2
Production of crystalline forms (specifically polymorphic forms or solvates) of enantiomers of modafinil (A) involves dissolving an enantiomer of (A) (preferably the levorotatory isomer, (-)-(A)) in a solvent other than ethanol, crystall...  
JP2011126825A
To provide an industrially practicable method for producing optically active L- or D-tert-leucinamide important as a raw material for a medicine or an agrochemical in excellent operability.The optical purity of the tert-leucinamide in a ...  
JP2010527345A5  
JP2011116780A
To provide processes for preparing 3-benzazepines and salts thereof [which can be useful as serotonin (5-HT) receptor agonists for the treatment of, for example, central nervous system disorders (such as obesity)], and to provide interme...  

Matches 1,001 - 1,050 out of 4,297