Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5929f2d6f4dba84be8dd3a8ba633db12 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-26 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D515-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-26 |
filingDate |
1973-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
1981-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb55c1bf46a98e7b550569874ce9ab9b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39256f6350613b83b606f5a27e832736 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a2774b3ac7b638c0030a9bdf07fb613 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_395a99312d3ea747ea105081304fd133 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d3f8bd800957a1e21cd451d4f199873 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6376557c44dd55561660ba538cc4dc8c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_993338a592e539f4d9cc21263154185a |
publicationDate |
1981-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
CA-1109860-A |
titleOfInvention |
Process for producing lactol-type cephalosporins |
abstract |
Process for producing Lactol-type Cephalosporins Abstract A 3-hydroxymethylcephalosporin which is not protected at the carboxyl group can be directly oxidized with a hexa-valent chromium compound to give in good yield a lactol type cephalosporin represented by the general formula: wherein R1 is hydrogen or an alkoxy group and R2 is an acylamino, or imido group. The resulting compounds are very useful and important as intermediates for preparing, e.g. 3-alkoxyiminomethyl cephalosporins. |
priorityDate |
1972-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |