| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b3c2e77f8dfda692ca527454d23ecc03 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 |
| filingDate |
1996-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
1998-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc8569d853a97d38ac8b9a6a31d7e8ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3dfc8c4676f651847a717a1c6ac47366 |
| publicationDate |
1998-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-5763607-A |
| titleOfInvention |
Preparation of optically-active isomers of dideoxycarbocyclic nucleosides |
| abstract |
A method is provided for preparing an antiviral compound of formula (I): <IMAGE> (I) wherein Y is CH, Z is H or NH2, and X is halo, comprising: (a) reacting a compound of formula (II): <IMAGE> (II) with triethylorthoformate, and (b) hydrolyzing the product of said reaction in the presence of acid to yield said compound of formula (I). |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9919327-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6870053-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6433170-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AP-1182-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6646125-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6641843-B1 |
| priorityDate |
1988-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |