Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_609a7477f1e3bac761d9ec2a65d85dcc http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_15b52fa7ebea0dcaa5791c66770b9fbf http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f077b668312e0625fde3663cb7f46a63 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_80a63b101a75d9e557e4db81a87fe113 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73d55b44219a84c850812a4488def924 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e23166138faace9037576f41e64e3663 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-06 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C247-04 |
filingDate |
2006-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5789e1f2d0c644349ed07ad7e5da504f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a76ad7f2d296e103d7dcb9d29b44282f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b22e4f8067b33a6832f6f1f22c42a139 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ba3306342be71525a04640f5e17a7ee |
publicationDate |
2007-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
WO-2007023583-A1 |
titleOfInvention |
Intermediate in synthesizing glycolipid derivative and method of producing the same, and glycolipid derivative and method of producing the same |
abstract |
To synthesize a glycolipid derivative typified by GGPL-III, it is required to efficiently synthesize an intermediate in synthesizing the glycolipid derivative represented by the general formula (VIII). For this purpose, it is needed to control both of the formation of an α-glycoside bond and the stereostructure of the glycerol moiety. A method characterized by involving the step of reacting a donor compound, which is a saccharide having a protective group introduced into an OH group other than the one at the 1-position thereof, with a phosphonium halogen compound and an optically active glycidol, which is employed as an acceptor compound, in the presence of a basic solvent to thereby control both of the formation of an α-glycoside bond and the stereostructure of the glycerol moiety. (VIII) In the general formula (VIII), R’s may be independently selected from among hydrocarbon groups; and Y’s may be independently selected from among protective groups of OH group and a hydrogen atom. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10232026-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009007279-A |
priorityDate |
2005-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |