http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002265490-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_33e6731073ff08ada5c5342556c035d2 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-073 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-067 |
filingDate | 2001-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_35555ec93cb659b8e6e73d7e528436e2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ceafc12e05c9cc8c3b01a27ede91dd69 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_568ffa8bf69915876c267058bb1a52f2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b84b64e7cb70dca19d99d787a366fea |
publicationDate | 2002-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2002265490-A |
titleOfInvention | Synthetic method of 2-thiouridine analog |
abstract | (57) [Summary] (with correction) [PROBLEMS] To provide a method for efficiently and efficiently synthesizing 2-thiouridine analogs from inexpensive compounds. SOLUTION: Protecting steps 10, 11, 12 for introducing a protecting group into a 3′-hydroxyl group, a 5′-hydroxyl group and a carbonyl group in a 4-position of a uridine analog, and after introducing a protecting group, a uridine analog. A functional group substitution step 13 for converting the 2-position carbonyl group into a thiocarbonyl group, and deprotection steps 14 and 8 for removing the protective group introduced in the protection step after performing the functional group substitution. A method for synthesizing 2-thiouridine analogs. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007153848-A |
priorityDate | 2001-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 99.