http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20090131731-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D309-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-18
filingDate 2008-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79a9c291a356ab72b17b4905129372ec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_576278074b507378949546380e00e548
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c7040ef1b170f8c1aa400d1a6014347
publicationDate 2009-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20090131731-A
titleOfInvention Optically active amino acid derivatives and preparation method thereof
abstract The present invention provides an optically active compound of formula 1 and a process for preparing the same:n n n <Formula 1>n n n n n n n n Wherein m is 0 or 1, R 1 is hydrogen or an amino protecting group, and R 2 together with adjacent nitrogen atoms form an aziridine or oxazolidinone ring, or is hydroxymethyl, or hydroxycarbonyl.n n n The compound of Formula 1 is an optically active compound having a dihydrofuran or a dihydropyran ring, which is introduced into the middle or the terminal of the biologically active peptide, and thus may be selectively cleaved or subsequently modified. Therefore, the compound of Formula 1 may be usefully used as an intermediate of synthetic peptides for functional proteins or functional analysis of proteins. In addition, the production method of the present invention can produce a compound of formula 1 having a stereo selectivity of 99% or more in high yield.
priorityDate 2008-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 31.