http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5132457-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb945eb5582e8ee65ed7517ad568b5c4 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C225-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C221-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C221-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C225-16 |
filingDate | 1991-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1992-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20e03244e1437318b560a578cc17f363 |
publicationDate | 1992-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-5132457-A |
titleOfInvention | Stereospecific synthesis of 2(R)-2-methyl-3-dimethylamino-propiophenone (d-DAMP) |
abstract | In a method for producing 2(R)-2-methyl-3-dimethylamino-propiophenone (d-DAMP), a chiral ester of the formula ##STR1## wherein R is an alkyl of from 1 to about 5 carbon atoms, is provided. The chiral easter of formula (I) is converted into a chiral amino-alcohol of the formula ##STR2## and the chiral amino-alcohol is oxidized so as to form d-DAMP. |
priorityDate | 1991-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 89.