http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2000169503-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fd569fbfa1953ca9b7b375510e4d2763 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H7-027 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B37-00 |
| filingDate | 1998-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b8782902d9771aac23e2dc09530ad25e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b86aff10c11f516d9d86df2d76b22872 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bfdeac9634fedc8d638ef7a160494272 |
| publicationDate | 2000-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2000169503-A |
| titleOfInvention | Method for producing sialic acid-containing oligosaccharide |
| abstract | (57) [Problem] To provide an organic chemical synthesis method of myelorollin and a synthetic intermediate useful for organic chemical synthesis of myelorollin. SOLUTION: The following (a) and (b) are subjected to a glycosidic bond reaction to obtain a Gal of (a) and a G of a non-reducing end of (b). A method for producing a sialic acid-containing oligosaccharide represented by the following formula (C), which may be protected with a protecting group, comprising at least a step of making lcNAc a glycoside bond. (A): (A) Wherein the functional group not involved in the reaction is protected with a protecting group, and the hydroxyl group involved in the reaction in Gal is substituted with a leaving group. (B): A sugar in which a functional group not involved in the reaction is protected by a protecting group in (B) in (D) in which R is glycoside-bonded to a secondary hydroxyl group of one or more constituent monosaccharides. (NeuAc is an N-acetylneuraminic acid residue, Gal is a galactose residue, GlcNAc is an N-acetylglucosamine residue, X is a hydrogen atom or a glucose residue,-is a glycosidic bond, -R is a monosaccharide residue R. A glycosidic bond to a secondary hydroxyl group of one or more constituent monosaccharides, m is 1 to 6) |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100413889-C http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004058984-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7304148-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8158763-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100736510-B1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2003296067-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2003296067-C1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2003296067-B8 |
| priorityDate | 1998-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 132.