http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002511839-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-117 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-70 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-655 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-117 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-46 |
| filingDate | 1998-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2002-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2002511839-A |
| titleOfInvention | Novel synthesis of MYO-inositol phosphate |
| abstract | (57) Abstract: Phosphate-based inositol derivative, 1-O-[(+)-menthoxycarbonyl] -6-O-benzyl-2,3: 4,5-di-O-isopropylidene-myo - inositol (D4P), D-myo- inositol 1, 4, 5 - triphosphate (D-IP 3), inositol 6-O-benzyl-2,3: 4,5-di -O- isopropylidene -myo - new synthesis of inositol -H- phosphonate (3-HP) and L-myo-inositol 1,4,5-triphosphate (L-IP 3) are provided. In these syntheses, fewer column chromatography steps were required for the isolation of intermediates than in conventional synthetic methods, and thus were simpler, more economical and more efficient than in conventional synthetic methods. It is efficient. |
| priorityDate | 1997-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 82.