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filingDate 1985-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22ecdba26829f37bd3d2ae17a98b34a4
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publicationDate 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6251694-A
titleOfInvention 3',4'-dideoxy-3'-fluorokanamycin b and production thereof
abstract NEW MATERIAL:The compound of formula I and its acid addition salt. n USE: Antibacterial agent. n PREPARATION: The objective compound can be produced by (1) reacting the 3'-deoxy-3'-fluoro-4'-O-sulfonylkanamycin B derivative of formula II (R is alkyl, aralkyl or aryl; Z is an amino-protecting group of the form of methoxycarbonyl, ethoxycarbonyl or benzyloxycarbonyl, an amino-protecting group of the form of alkanoyl or aroyl or an amino-protecting group of solfonyl-type; B is an amino-protecting group of the form of alkylsulfonyl, aralkylsulfonyl or aryl- sulfonyl; X and Y are H or univalent OH-protecting group, X and Y may together form a bivalent OH-protecting group; Q is alkylsulfonyl, aralkylsulfonyl or arylsulfonyl same as the group B; V is OH-protecting group) with a metal halide of formula MD (M is metal; D is Cl, Br or I), (2) reducing the obtained 4'-halogenated product to substitute the 4'-halo group with H and (3) eliminating the protecting groups A, B, Q, V, X and Y. n COPYRIGHT: (C)1987,JPO&Japio
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priorityDate 1985-08-29-04:00^^<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.