http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2015172024-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_11a792d7816d4692078e29ef27bfa056 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-58 |
| filingDate | 2014-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_853721268c3ca5d1f0397f9a66ba0c74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85ad15037cd797fa168ca46816190bb9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00a0d4250264b18d849dd88efcc247bb |
| publicationDate | 2015-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2015172024-A |
| titleOfInvention | Chiral bicyclic diene ligands with hydrogen bond-forming amide groups |
| abstract | A chiral bicyclic diene ligand having a tert-butylamide group contributing to the formation of a hydrogen bond and a chiral transition metal complex for obtaining an optically active substance more efficiently are provided. A chiral bicyclic diene ligand represented by the formula (1) and a chiral late transition metal complex purified by the reaction formula represented by the formula (2). (R 1 to R 3 are H, an alkyl group, or an alkoxy group; n is a methylene chain of 0 or 1; M is a late transition metal species; L is a coordination that can be exchanged with a ligand of the formula (1). Child) [Selection figure] None |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019126751-A |
| priorityDate | 2014-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 56.