http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20040029575-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6ce9572cb248acfb97a5a830251b71af
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H1-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-23
filingDate 2002-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bad209f608b76dea793ac4e44d2e8d7e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba71d16e7241c403a8abc5e18f9209f7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac4d3ffb4aa658debb3994f415395c68
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publicationDate 2004-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20040029575-A
titleOfInvention Process for preparing Isepamicin
abstract The present invention relates to a method for preparing isepamycin, and more particularly, by using sisomycin or gentamycin with a smooth supply of raw materials as a starting material, the purpurosamine or sisosamin ring is removed and 1- Semi-synthetic method of glycosidation of the carmine derivative and glycosyl chloride via a caramine derivative synthesized by binding isoserine derivative to NH 2 position as a reaction intermediate. The present invention relates to a method for effectively preparing isepamycin represented by the following formula (8).
priorityDate 2002-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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