http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H10182684-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_129e393582e6bdf4029baf2206522f45
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-207
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
filingDate 1996-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_edb3485169e70ea4cade8b28b3c5255f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc67bd6d2075b1d32cff63b75c8c1fb0
publicationDate 1998-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H10182684-A
titleOfInvention New glycosylation method
abstract (57) [Solution] When a glycoside compound is obtained by reacting a thioglycoside derivative having a protected hydroxyl group with a hydroxy compound, the reaction is carried out in the presence of an acid catalyst, an oxidizing agent and a dehydrating agent. A new glycosylation method that can be used. [Effect] Mild use of a combination of a small amount of acid catalyst, oxidizing agent and dehydrating agent without using heavy metals or reagents having problems such as irritation, explosiveness, hygroscopicity and carcinogenicity. Under the conditions, the glycosylation reaction of a hydroxy compound using a thioglycoside as a donor proceeds smoothly, and α- or β-glycosides can be obtained in high yield and high stereoselectivity.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0042057-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008266292-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008239601-A
priorityDate 1996-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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