http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007254418-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d93502a23a72b56472bc75854cfe7c60
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-93
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-30
filingDate 2006-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1c146c0819f69ce5156b426c562561ca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7d475003a55b70182db4a02962cb062
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publicationDate 2007-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2007254418-A
titleOfInvention Method for producing optically active lactone compound
abstract The present invention provides a method for producing an optically active lactone compound, which can industrially advantageously produce an optically active lactone compound. The step of reacting an optical isomer mixture of a lactone compound with an amine compound to obtain an optical isomer mixture (A) of a hydroxycarboxylic acid amide, the mixture (A) is a bicyclo [3.3.0]. ] A step of reacting with a 2-oxa-1-octane compound to obtain a diastereomer mixture (B), a step of separating the mixture (B) into each diastereomer, and decomposing the separated diastereomer to obtain an optical A method for producing an optically active lactone compound comprising a step of obtaining an active hydroxycarboxylic acid amide (C) and a step of obtaining an optically active lactone compound by hydrolysis and ring-closing reaction of the hydroxycarboxylic acid amide (C). [Selection figure] None
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priorityDate 2006-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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