http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5663993-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-234
filingDate 1979-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce03f3e4c316a7c744a4d6552acd3a2e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92b5dbdbb2968008aeb158620c8ee760
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publicationDate 1981-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5663993-A
titleOfInvention Novel preparation of tobramycin
abstract PURPOSE: To prepare the titled compound useful as an antimicrobial agent, etc., economically, in an industrial scale, by reacting a specific 3'-O-sulfonylated kanamycin B protected derivative with a metal halide, reducing the 3'-halo group, and then eliminating the protecting group. n CONSTITUTION: A 3'-O-sulfonylated kanamycin B protectd derivative of formula I (R is hydrocarbon; Y is 1W6C alkylidene, etc. which acts as a bivalent PH-protecting group; Z is arylsulfonyl which acts as amino-protecting group) is made to react with a metal halide of formula MX (M is metal; X is Cl, Br or I) to obtain a 3'-halogenated product of formula II. The objective compound is prepared by reducing the compound of formula II to 3'-deoxykanamycin B protected derivative wherein the 3'-halo group is substituted by hydrogen, and if necessary, eliminating the remaining amino-protecting group and hydroxyl-protecting group from the product by conventional process. n COPYRIGHT: (C)1981,JPO&Japio
priorityDate 1979-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 23.