http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-5372556-B2
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-732 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-23 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C241-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C243-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-19 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-343 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-42 |
| filingDate | 2009-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2013-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2013-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-5372556-B2 |
| titleOfInvention | Production method of selective homoallylic alcohol derivatives by α-addition type allylation reaction |
| abstract | <P>PROBLEM TO BE SOLVED: To provide a method for highly stereoselectively producing a homoallyl compound in a high yield by an optically active α-addition-type allylation reaction. <P>SOLUTION: The α-addition-type allylated compound is stereoselectively produced by a catalytic asymmetric α-addition-type allylation reaction where an allylborane compound is caused to react with a carbonyl compound or a hydrazone derivative thereof in the presence of a metal catalyst in the presence or absence of a ligand in a mixed solvent of water with an organic solvent. For example, in the case of a carbonyl compound, an α-adduct compound 4a is obtained in a high yield by the reaction of the formula below in the presence of metal Zn and 2,9-dimethylphenanthroline (Ligand 3). <P>COPYRIGHT: (C)2010,JPO&INPIT |
| priorityDate | 2009-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 142.