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filingDate 1998-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8f824b73d60328f529da7cdeee75d35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_995055086975c35ae8ddd9a2be9f0e5d
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publicationDate 2000-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20000022106-A
titleOfInvention Method for preparing β-lactam antibiotics
abstract The present invention relates to a process for preparing β-lactam antibiotics, wherein the N-substituted β-lactam or a salt thereof having the formula (I) is contacted with at least one dicarboxylate acyla or functional equivalent thereof: And react with precursors to the side chains of β-lactam antibiotics in the presence of at least one penicillin acylase or functional equivalent thereof:n n n Formula In n n n n n n n In the above formula,n n n R 0 is hydrogen or C 1-3 alkoxy; Y is the oxidation form of CH 2 , oxygen, sulfur or sulfur; Z is the following (a), (b), (c) and (d)n n n n n n n n Wherein R 1 is hydrogen, hydroxy, halogen, C 1-3 alkoxy, saturated or unsaturated, branched or straight chain C 1-5 alkyl, preferably methyl, optionally substituted with one or more optionally containing one or more heteroatoms C 5-8 cycloalkyl substituted, optionally containing one or more heteroatoms, optionally substituted aryl or heteroaryl, or optionally substituted benzyl; And X is (CH 2 ) m -A- (CH 2 ) n , where m and n are the same or different and are selected from the group of integers 0, 1, 2, 3 or 4, and A is CH = CH, C ≡C, CHB, C═O, optionally oxidized form of optionally substituted nitrogen, oxygen, sulfur or sulfur, and B is hydrogen, halogen, hydroxy, C 1-3 alkoxy or optionally substituted methyl.
priorityDate 1997-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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