| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a5a95d4999542f2d9fa147bfed0e90cf |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-0803
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-08 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-044
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-02 |
| filingDate |
1992-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_861e12c85b3125305053425d3be6fc85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e998f5b9dab7ef495ecfa45cd3690f9 |
| publicationDate |
1994-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-0589965-A1 |
| titleOfInvention |
NOVEL ORGANOBORE REAGENTS FOR THE PREPARATION OF NON-SUBSTITUTED PROPARGYL ALCOHOLS. |
| abstract |
The novel organobore reagent of the present invention is used for the preparation of unsubstituted propargyl alcohols. This compound provides a clean reaction with aldehydes and ketones and produces propargyl alcohols in excellent yields. Unsubstituted propargyl alcohols are important synthetic intermediates for the synthesis of a number of natural products. In addition, the new organobore reagent exhibits diastereomeric selectivity when it is reacted with aldehydes characterized by an enantiomeric purity. |
| priorityDate |
1991-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |