http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-232710-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_334f3ee6eeb9c496c3cce8c9fc4532f0 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H5-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H13-04 |
filingDate | 1984-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f0f75850510fd16dc7066931b0a66cd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee457bb7f8a370123d07260bd0630e6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55df880e9e8e1f3f23fc0a515917db9c |
publicationDate | 1986-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | DD-232710-A1 |
titleOfInvention | PROCESS FOR THE PREPARATION OF FURANDERIVATES |
abstract | The aim of the invention is to develop a process for the preparation of acylated 2-cyano-3- (fur-2-ylmethylamino) -3- (b-D-glycofuranosyl or glycopyranosylthio) acrylic acid esters. The furan derivatives of the general formula III in which R is an alkyl radical and R 1 is an acylated glycofuranosyl or glycopyranosyl radical can be prepared by reacting the furylmethylammonium salts of the general formula I in which R has the above meaning, with acyl halogens of the general formula II wherein R1 is as defined above and X is a halogen atom. The furan derivatives can be used as organic intermediates for further syntheses. They are particularly suitable for the preparation of specific nucleoside analogs. |
priorityDate | 1984-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 20.