http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H08119890-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-143
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-46
filingDate 1994-10-25^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47fa08e2b89504ae1b87610343ebf9f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2576e5b72ad999294cc01901fa68a6d1
publicationDate 1996-05-14^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08119890-A
titleOfInvention Method for producing optically active alcohol
abstract (57) [Summary] (Modified) [Structure] 3'-Substituted phenyl bromomethyl ketone was prepared by a complex obtained by reacting (1S, 2R) -1,2-diphenyl-2-aminoethanol with borane. (R) -3 ′ of the optically active general formula II characterized by being reduced -Method for producing substituted phenyl bromomethyl carbinol. (X represents a fluorine atom, a chlorine atom, a bromine atom, a methoxy group or an ethoxy group.) [Effect] High yield and high yield of (R) -3′-substituted phenylbromomethylcarbinol, which has been difficult to synthesize by conventional methods. It can be manufactured with optical purity.
priorityDate 1994-10-25^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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