http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103936596-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B43-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02 |
| filingDate | 2014-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103936596-B |
| titleOfInvention | The method of the amino alcohol catalyze imine reduction that sugar is derivative |
| abstract | The invention discloses the method for the amino alcohol catalyze imine reduction that a kind of sugar derives: take imines as substrate, comprise the following steps successively: 1), be dissolved in organic solvent I by the aminoalcohol catalyst that imines and sugar derive, the mol ratio of the aminoalcohol catalyst that described imines and sugar derive is 100:1 ~ 20; 2), in the solution of step 1) gained drip 1.5 ~ 5 times of equivalents trichlorosilane after, at-20 ~ 40 DEG C after stirring reaction 12 ~ 36h, then use saturated sodium bicarbonate solution cancellation; 3), by step 2) gains organic solvent II extract, column chromatography for separation, obtained aminated compounds. |
| priorityDate | 2014-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 66.