http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105665011-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d94573ab2c57e8b193f3a22accddf9fe |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2231-00 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C323-43 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0275 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C391-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0245 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-64 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C391-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-43 |
| filingDate | 2016-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a73bf48316dd646614c928d900358bd1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de98a528a2a5f553f1676fadb97e0780 |
| publicationDate | 2016-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-105665011-A |
| titleOfInvention | Chiral organic selenium-sulfur catalyst and its preparation method and use in asymmetric reaction |
| abstract | The invention discloses a chiral organic selenium-sulfur catalyst and its preparation method and use in an asymmetric reaction. The chiral organic selenium-sulfur catalyst is prepared from commercial and low price chiral amino-indanol through high efficiency multi-step synthesis. The preparation method has simple processes and is convenient for operation. The chiral organic selenium-sulfur catalyst based on an organic indene skeleton has a wide application range, good catalysis effects in many organic reactions and excellent enantiomer selectivity. The chiral organic selenium-sulfur catalyst has excellent optical selectivity in an asymmetric trifluoromethylthioesterification reaction, opens the ancient river of an alkene asymmetric trifluoromethylthioesterification reaction and has high catalysis efficiency and good enantioselectivity. |
| priorityDate | 2016-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 74.