http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107365359-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K9-008 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K9-00 |
| filingDate | 2017-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-107365359-B |
| titleOfInvention | Synthesis method of vancomycin chiral functional monomer |
| abstract | The invention relates to a synthesis method of a vancomycin chiral functional monomer, and belongs to the technical field of organic synthesis and synthesis of functional high polymer intermediates. Completely dissolving vancomycin in an organic phase, and then adding an acyl chloride compound, wherein the molar ratio of the vancomycin to the acyl chloride compound is as follows: 1.0: 1.0-2.5, reacting for 0.5-4.0 h at the temperature of 0-80 ℃ to obtain vancomycin chiral functional monomer VanR, wherein Van represents vancomycin, and R represents a group substituted on vancomycin and is an alkylene group. The vancomycin derivative synthesized by the method contains terminal alkenyl in the structure, and can be used as a valuable functional monomer in the preparation of high molecular polymers. |
| priorityDate | 2017-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 28.