http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107628998-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_53b4d53983adbf56dd0e7d0bf96f8ce5 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-20 |
| filingDate | 2017-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_053b94c0aec5db7d4ba8346770610431 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd3c987381a57b9c623125d8742da773 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69fd42b5193752a1c634f84bc0f101eb |
| publicationDate | 2018-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-107628998-A |
| titleOfInvention | A kind of preparation method of lepadin alkaloid synthetic intermediate |
| abstract | The invention provides a highly efficient preparation method for a class of cis-decahydroquinoline compounds with general formula (I). Starting from the readily available compound A, the compound of general formula (I) can be conveniently obtained through key steps such as Diels-Alder reaction and catalytic hydrogenation. Using this method to prepare the compound of general formula (I) and using it as a key intermediate to synthesize (–)-lepadins A-C and its derivatives can make the whole synthesis yield ideal and the steps simple. Compared with the previously reported synthesis of (–)‑lepadins A‑C, the steps are obviously shortened, the yield is improved, the cost is reduced, and it has a good application prospect. |
| priorityDate | 2017-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 18.