http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20040063264-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N1-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-002
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
filingDate 2003-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61fc0e6bfcd72299e282e5aac414542a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fcd316d9343858dddec94514a65245ea
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publicationDate 2004-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20040063264-A
titleOfInvention Method for preparing optically active (R)-2-chloromandelic acid and its ester derivatives using Baker's Yeast
abstract The present invention relates to a method for preparing optically active (R) -2-chloromandelic acid ((R) -2-chloromandelic acid) and ester derivatives thereof using yeast (Baker's Yeast), and more specifically, to a phosphate buffer. Optical activity (R) -2-chloromandelic acid by biological method for selectively reducing alkyl 2-Chloro-benzoylformate in the presence of a solution using Baker's yeast and its It relates to a method for producing an ester derivative. The production method of the present invention uses yeast, which is inexpensive and easy to obtain, which makes the manufacturing process simple and economical, and has high optical purity and yield.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100752282-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11450245-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100722155-B1
priorityDate 2003-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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