http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5157167-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a5a95d4999542f2d9fa147bfed0e90cf |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-0803 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-08 |
| filingDate | 1992-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1992-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e998f5b9dab7ef495ecfa45cd3690f9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_861e12c85b3125305053425d3be6fc85 |
| publicationDate | 1992-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-5157167-A |
| titleOfInvention | Organoboron reagents for the preparation of unsubstituted propargylic alcohols |
| abstract | The novel organoboron reagent of the present invention is useful in the preparation of unsubstituted propargylic alcohols. This compound reacts with aldehydes and ketones cleanly to afford propargylic alcohols in excellent yields Unsubstituted propargylic alcohols are important synthetic intermediates in the synthesis of a number of natural products. In addition, the novel organoboron reagent of the present invention also demonstrates diastereomeric selectivity when reacted with enatiomerically pure aldehydes. |
| priorityDate | 1991-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 144.