http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20110080659-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a6209e5a437bf57ab1a4d6d690e27f42 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-357 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-94 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-94 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04 |
| filingDate | 2010-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99594dd38da149188248914a8a336200 |
| publicationDate | 2011-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20110080659-A |
| titleOfInvention | Efficient synthetic method for sumadain a and its derivatives |
| abstract | PURPOSE: A novel synthetic method for sumadain A or derivative thereof is provided to quickly and efficiently prepare sumadain A and derivative thereof with excellent physiological activity. CONSTITUTION: A method for synthesizing sumadain A or derivative thereof comprises: a step of cyclizing 2,4,6-trihydroxyacetopenone and alpha,beta-unsaturated aldehyde under the presence of diacetate at 90-110°C for 8-12 hours; and a step of performing aldole condensation reaction of the reactant with benzaldehyde at room temperature for 42-56 hours. The sumadain A or derivative thereof is denoted by chemical formula 1 or 2. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104370933-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104370933-A |
| priorityDate | 2010-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 46.