http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006000006-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P13-04
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filingDate 2004-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_765e30ec7a7bb63747813174dffcd4c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8c76f38b2ad84114cbbb0077c169347
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publicationDate 2006-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2006000006-A
titleOfInvention Process for producing optically active 2-alkyl-D-cysteine ester
abstract 【Task】 Provided is an economical and industrially feasible production method for optically active 2-alkyl-D-cysteine esters important as production intermediates for various industrial chemicals, agricultural chemicals and pharmaceuticals. [Solution] A 2-alkylcysteine amide is reacted with a microbial cell or a treated product of a microorganism having an activity of stereoselectively hydrolyzing the amide bond of 2-alkyl-L-cysteine amide to produce 2-alkyl cysteine as a product. A mixture of L-cysteine and unreacted 2-alkyl-D-cysteine amide, which is reacted with an aldehyde, ketone, or acetal (ketal) to give thiazolidine-4-carboxylic acid and thiazolidine-4-carboxylic acid After separation of thiazolidine-4-carboxylic acid amide from the mixture, ring opening and hydrolysis yielded 2-alkyl-D-cysteine, which was esterified to give 2-alkyl-D-cysteine Esters are produced.
priorityDate 2004-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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