http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63222156-A

Outgoing Links

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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
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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
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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

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Total number of triples: 22.