http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105688858-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2220-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2220-80 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J20-29 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J20-29 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J20-30 |
| filingDate | 2016-02-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2018-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2018-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-105688858-B |
| titleOfInvention | A kind of Amylose Chiral Stationary Phase and preparation method thereof |
| abstract | The present invention relates to Polysaccharides Type Chiral Stationary Phases technical fields, disclose a kind of silica gel and prepare the method that triazolyl is bonded amylose and its derivative chiral stationary phase by click-reaction.The present invention is handled by the alkynyl that 6 hydroxyls of amylose are carried out with selective modification and silica gel, using efficient catalyst, is prepared for bonding type amylose and its derivative chiral stationary phase.The chiral stationary phase shows the fractionation ability excellent to various chiral racemies in liquid chromatogram, can be applied to various chiral chromatogram column packings field because amylose and its derivative have the space structure of high-sequential and intrinsic chiral environment. |
| priorityDate | 2016-02-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 69.