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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
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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

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