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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
filingDate 2003-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c52e3e3b952ea2da2bba7a20cc139a6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96425665c26a9b8e5b32221534bfb79f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf823fc48cbd81b8b7b9ebcc706a69d4
publicationDate 2004-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20040089887-A
titleOfInvention Process for preparing Epothilone derivatives
abstract The present invention relates to a method for preparing an epoxylon derivative, and more particularly, by specifically designing the structure of the aldehyde compound and the ketone compound to be used in the aldol condensation reaction, the ratio of the desired isomer in the isomer is absolute. Due to the characteristics of a series of manufacturing methods, such as synthesizing so that the isomers can be easily separated by synthesizing to have an advantage, a method for preparing a high-purity and high-yielding Epothilone derivative as a next-generation anticancer agent will be.
priorityDate 2003-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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