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Matches 951 - 1,000 out of 4,297

Document Document Title
JP4995728B2  
JP4994427B2  
JP2012136480A
To provide a new optically active macrocyclic compound capable of identifying asymmetry of an asymmetric compound, especially, capable of identifying asymmetry of an asymmetric compound incapable of hydrogen-bonding, to provide a product...  
JP2012131785A
To provide a method for producing optically-active menthol, which is composed of a few steps that are all catalytic reaction steps, therefore producing little environment-polluting waste, and can achieve a reduction in the manufacturing ...  
JP4975450B2  
JP2012515142A
A process for manufacture of 2* acylamino *3* diphenyl propanoic acid and an intermediate useful to composition of a compound active in medicine, especially neutral endopeptidase (NEP) inhibitor, and division.  
JP2012515187A
A way the present invention separates the エナンチオマー mixture of the (R) - and (S) -3-amino 1-butanol from which the oxygen atom was protected by the case, And it is related with the method of essentially preparing (R) -3-amino...  
JP4966449B2  
JP4966933B2  
JP4961562B2  
JP2012514005A
The present invention provides the new method of the 2* amino * tetrahydro carbazole * propanoic acid composition which is the important synthetic intermediate of Lamaism トロバン. In detail, amino cyclohexanol is oxidized and amino ...  
JP4954886B2  
JP4956614B2  
JP4954378B2  
JP2012106997A
To provide a novel process for producing an optically active 4-chloro-3-hydroxybutanal compound.The process for producing the optically active 4-chloro-3-hydroxybutanal compound (2) includes a step of making chloroacetaldehyde and an ald...  
JP2012107067A
To provide methods and intermediates for the preparation of 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.Se...  
JP2012512172A
The present invention relates to dialdehyde useful to stereoselective synthesis or a dinitrile compound of piperidine, pyrrolidine, and a アゼパン derivative. [Chosen drawing] Nothing  
JP2008530180A5  
JP2012102032A
To provide a purification method capable of obtaining optically active 1,1,1-trifluoro-2-propanol with high purity.The optically active 1,1,1-trifluoro-2-propanol with high purity can be obtained by reacting with an aralkyl halide a mixt...  
JP4942656B2  
JPWO2010067824A
Inhibitory action of the Xth factor of activation blood coagulation was shown, and offer of a method which manufactures industrially an intermediate of a compound useful as a prevention agent and/or a medical treatment agent of a thrombo...  
JP4927258B2  
JP2012082223A
To provide a method for efficiently producing a monatin useful as a sweetener, especially an optically active monatin.A monatin whose 2-position and 4-position configurations are different from each other is subjected to isomerization of...  
JP2012072151A
To provide a compound useful for preparing caspase inhibitors and/or prodrugs thereof.The invention relates to processes and compounds useful for producing modified aspartic acid derivatives, such as aspartic acid aldehyde moieties. Aspa...  
JP4916064B2  
JP4915019B2  
JP2012508162A
The present patent application relates to an alternative process for the preparation of amino derivatives. In particular, the present application relates to an improved process for the manufacture of Lacosamide (LCM), (R)-2-acetamido-N-b...  
JP2012508235A
amino alcohol lipid -- manufacture by making amine of an id react to the EPO キシド end compound is indicated. amino alcohol lipid -- the method for preparing an id from a commercial starting material is also provided. amino alcohol l...  
JP2012067122A
To provide a method for producing enantiomerically pure 4-pyrrolidinophenylbenzyl ether derivatives.In this method, a pyrrolidine-3-carboxylic acid type racemic body is resolved by a resolving agent, then transformed into corresponding p...  
JPWO2010050499A
The present invention adds a specific quantity of alkali to a mirror image isomer mixture of optical activity organicity carboxylic acid which has deviation in a mirror image isomer's existence molar ratio, Or a thing a specific quantity...  
JPWO2010050499A1
本発明は、鏡像異性体の存在モル比に偏りが ある、光学活性有機カルボン酸の鏡像異性体 混合物に、特定量のアルカリを加えることに より、または該光学活性有機カルボン酸...  
JP4906511B2  
JP4898658B2  
JP2012051820A
To provide a novel optical resolving agent comprising an optically active azulene derivative which facilitates separation in column chromatography by observation with the naked eye, and a novel method for producing optically active alcoh...  
JP4896294B2  
JPWO2010041739A1
本願発明は、安価に入手し易く安全な原料を 用いて、高収率及び高光学純度にて光学活性 ビニルシクロプロパンカルボン酸誘導体を得 る方法を提供することを課題とする。更...  
JP2012044931A
To provide a method for producing an optically active amino acid and an optically active amino acid amide in a good efficiency.This method for producing the optically active amino acid and optically active amino acid amide by bringing th...  
JPWO2010041739A
The invention in this application makes it a subject to provide a method of obtaining an optical activity vinyl cyclopropane carboxylic acid derivative in quantity 収率 and the Takamitsu study purity, using safe materials that it is ea...  
JP4892195B2  
JP2012505183A
The present invention describes a novel process for the preparation of optically active (S)-(-)-2-(N-propylamino)-5-methoxytetraline and (S)-(-)-2-(N-propylamino)-5-hydroxytetraline compounds based on the optical resolution of mixtures o...  
JP4887720B2  
JP4874122B2  
JP2012025705A
To provide a method for simply producing (S)-4-[(4-chlorophenyl)(2-pyridyl)methoxy]piperidine by high-yielding and excellently operable optical resolution.An optically active dicarboxylic acid selected from among di-p-toluoyl-D-tartaric ...  
JP4871887B2  
JP4868301B2  
JP4856070B2
The present invention relates to a method for the chemical separation of the enantiomers of 1,1'-spirobiindane-6,6'-diol derivatives comprising providing a racemic chiral 1,1'-spirobiindane-6,6'-diol derivative, reacting a nonracemic chi...  
JP2009149600A5  
JP4853834B2  
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...  

Matches 951 - 1,000 out of 4,297