http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H10279572-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e83d93ed02bbd6159e99b5a7796e3686 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2602-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D281-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C219-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D303-48 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D281-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C219-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D301-03 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-48 |
filingDate | 1998-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a3bd4035ead4f9fde19799e68ae7aaf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b02a83e8bf0a4e83aede6f6e17d46a65 |
publicationDate | 1998-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H10279572-A |
titleOfInvention | Method for producing optically active phenylglycidylic acid derivative |
abstract | [PROBLEMS] To produce a trans-phenylglycidyl derivative with a high pyramidal or diastereomeric ratio. (wherein, R represents a substituted or unsubstituted phenyl group, preferably p- methoxyphenyl represents phenyl) in an optically active acetyl compound having the following formula (3) X-CH 2 -COOA (3) ( wherein, X Is a leaving group, and A is an amino alcohol having a rigid structure, preferably derived from β-amino alcohol), and is contacted in the presence of a base to give an optically active trans compound having the following formula (1). -Compounds (Where R represents a substituted or unsubstituted phenyl group, preferably p-methoxyphenyl), and A is derived from an optically active compound. Particularly preferred A is amino having the following formula (4) Indanol compound. (Here, R 1 and R 2 each represent a substituted or unsubstituted (hetero) alkyl or (hetero) aryl group having 1 to 10 carbon atoms.) |
priorityDate | 1997-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 31.