| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e83d93ed02bbd6159e99b5a7796e3686 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C249-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C227-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-52 |
| classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C251-08 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C249-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-27
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00 |
| filingDate |
2001-05-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21165540c65cb63eaa4e33ae3416f307
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bd29c26e73fe0020f3d24fcdaf94e88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22958339882fea513db1fd4fce562c02 |
| publicationDate |
2003-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-1283824-A1 |
| titleOfInvention |
Preparation of enantiomerically enriched amine-functionalized compounds |
| abstract |
Process for removing a residual fragment of a chiral auxiliary from a diastereomeric compound with formula (2) in the preparation of an enantiomerically enriched, amine-functionalized compound, with the diastereomeric compound being subjected to a non-reductive removal of the residual fragment of the chiral auxiliary, the carbon atom that is removed having an oxidation state of +3 which is not lowered during the method of removal. The chiral auxiliary is preferably chosen from the group of amides or esters of proteogenous amino acids or from the group of phenylglycine amide, an ester of phenylglycine, p-OH-phenylglycine amide, an ester of p-OH-phenylglycine, α-methylphenylglycine amide and an ester of α-methylphenylglycine. |
| priorityDate |
2000-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |