http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63222156-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_01c1e0bc0628f76dea731cda5a666ca1 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18 |
filingDate | 1987-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd5f707728f7eee1f2296d48d12256fb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8043c3660f369a10a36415466c0a9d84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0d1c0c3f085dda6b6ad503fc92fddf5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ea45cd80f9d955df0167686da0f4d62 |
publicationDate | 1988-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-S63222156-A |
titleOfInvention | Beta-lactam intermediate |
abstract | NEW MATERIAL:Optically active 4-alkoxyazetidin-2-one compound of formula I (R 1 is hydroxyl-protecting group; R 2 is H or amino-protecting group; R 3 is 1W4C aliphatic hydrocarbon group). n EXAMPLE: (3R,4R,5R)-3-[1-(t-butyldimethylsiloxy)ethyl-4-methoxy-azetidin-2-one. n USE: A synthetic intermediate for penem-type β-lactam antibiotic substance. The compound is characterized by the presence of alkoxy group at 4-site. n PREPARATION: The compound of formula I can be produced by reacting 3-[1-(t- butyldimethylsiloxy)ethyl]-4-acetoxyazetidin-2-one of formula II with sodium alcoholate as a base in an alkanol. n COPYRIGHT: (C)1988,JPO&Japio |
priorityDate | 1987-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 22.