http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102585040-B
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d94573ab2c57e8b193f3a22accddf9fe |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B37-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03F7-004 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-06 |
filingDate | 2012-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2015-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_12a95a0f4f21d11aff3d9f72293add49 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0101e5e191dd8388d76142b2eb3856e5 |
publicationDate | 2015-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-102585040-B |
titleOfInvention | Beta-cyclodextrin derivative based on annular alkamine as well as preparation method and application of beta-cyclodextrin derivative |
abstract | The invention discloses a beta-cyclodextrin derivative based on annular alkamine as well as a preparation method and an application of the beta-cyclodextrin derivative. The beta-cyclodextrin derivative is mono (6-(2-hydroxyl hexanaphthene amino)-6-deoxidation)-beta-cyclodextrin (CD-1), mono (6-(3-hydroxyl hexanaphthene amino)-6-deoxidation)-beta-cyclodextrin (CD-2), mono (6-(4-hydroxyl hexanaphthene amino)-6-deoxidation)-beta-cyclodextrin (CD-3), mono (6-(2-hydroxyl cyclopentyl amino)-6-deoxidation)-beta-cyclodextrin (CD-4) and mono (6-(3-hydroxyl-4-amino tetrahydrofuran)-6-deoxidation)-beta-cyclodextrin (CD-5). The beta-cyclodextrin derivative can be prepared from mono (6-O-p-tosyl group)-beta-cyclodextrin and corresponding annular alkamine to take nucleophilic substitution reaction in polar aprotic solvents. A synthetic method has the advantages that the operation is simple, the reaction condition is mild, the yield is high, and the like. The beta-cyclodextrin derivative can be used as a water-soluble ligand of metal imitation enzymes to be applied to water phase metal catalytic organic synthesis, water phase molecular recognition and water phase photosensitive materials. |
priorityDate | 2012-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 63.