http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009256273-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_716e9a2606ffd4ba1a2a3917e4a402fd http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fc6220b93fae4be14ada49e4ecc1860b |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H5-10 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18 |
filingDate | 2008-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eec639b9f516359be624439a3b5f07e6 |
publicationDate | 2009-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2009256273-A |
titleOfInvention | Method for introducing regioselective protecting group of alkyl β-D- (thio) glucopyranoside derivative |
abstract | A method for regioselectively introducing different protecting groups into various hydroxyl groups of alkyl β-D- (thio) glucopyranoside derivatives is provided. (1) General formula [4] (Wherein R 1 represents an alkyl aralkyl group, represents an R 2 acyl group, and X represents O or S) and TBDSX 1 (wherein X 1 represents halogen) and Then, this is reacted with di-tert-butyl dicarbonate in the presence of a pyridylpyrrolidine catalyst, and further reacted with BOMX1 to give the general formula [7] The manufacturing method and compound of a compound shown by these. [Selection figure] None |
priorityDate | 2008-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 162.