http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111171085-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H9-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-18 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H9-04 |
| filingDate | 2020-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-111171085-B |
| titleOfInvention | A rhamnose donor protected by orthocarbonate and its preparation method and application |
| abstract | The invention belongs to the technical field of chemical synthesis, and relates to a rhamnose donor and its preparation method and application. The structural formula of the rhamnose donor is as follows: Wherein, R 2 is an acyl group; LG is a leaving group. The beneficial effects of the present invention are: using the prepared orthocarbonate-protected rhamnose donor, the rhamnose β-glycosidic bond is efficiently constructed through the change of the sugar ring conformation and the remote participation of the acyl group, and the orthocarbonate protection is realized removal. |
| priorityDate | 2020-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 110.