http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4002609-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_515c496553231850a0e32150053788e7 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H13-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H13-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H13-04 |
| filingDate | 1975-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1977-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b32817bf30aad65145db0f6d30356e1 |
| publicationDate | 1977-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-4002609-A |
| titleOfInvention | Sucrose derivatives |
| abstract | Two sucrose hepta-acetates, useful as synthetic intermediates in the preparation of functional sucrose derivatives, are obtained by tritylating sucrose, acetylating the resulting mixture of monotritylsucroses, and detritylating the resulting mixture of monotritylsucrose hepta-acetates. The previously known compound, 1',2,3,3',4,4',6-hepta-O-acetylsucrose, can be recovered by crystallization from the solution obtained in the detritylation step. When the remaining solution is subjected to retritylation and chromatography, it yields a new compound, 1',2,3,3',4',6,6'-hepta-O-acetylsucrose. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4801700-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5141860-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5116961-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4307229-A |
| priorityDate | 1974-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 43.