http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0332047-A2
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_db7324dd156e7b5744b5c160e3f02ccf |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D313-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D313-00 |
filingDate | 1989-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f61d073ee1c65b7e82b4cdbee344c014 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71aa162a2939a782311b9ea7e07e8b84 |
publicationDate | 1989-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-0332047-A2 |
titleOfInvention | A process for the separation of macrocyclic diastereomers |
abstract | A process for the separation of the two diastereomers (3S,7R) and (3S,7S)-3,4,5,6,7,8,9,10,11,12-decahydro-7,14,16-trihydroxy-3-methyl- 1H -2-benzoxacyclotetradecin-1-one (α- and β-zeranol), of formulae Ia and Ib:n starting from the mixture thereof, which contains 50-60% diastereomer Ia, by means of crystallization from acetonitrile containing 0.2-2% water, under controlled cooling conditions, to obtain compound Ia ( α-zeranol) with a diastereomeric purity (titre) higher than 98.5%. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8674120-B2 |
priorityDate | 1988-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 51.