Predicate |
Object |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C229-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-21 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P37-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P35-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P35-06 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-43 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-18 |
filingDate |
2008-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate |
2010-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
JP-2010520752-A |
titleOfInvention |
Process for the preparation of beta-lactam compounds |
abstract |
The present invention provides a semi-synthesis from a nucleus, a side chain selected from the group consisting of D-phenylglycine and D-dihydro-phenylglycine in the form of a side chain ester, and an enzyme that catalyzes the conjugation of the side chain ester and the nucleus. In the method for synthesizing the β-lactam compound, a method is described in which the side chain ester is not isolated as a solid intermediate. [Selection] Figure 1 |
priorityDate |
2007-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |