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pubmed-article:7275833pubmed:abstractTextThe four amino groups of fortimicin B(4) could be differentiated from each other and 2'-N-benzyloxycarbonyl-, 2',6'-di-N-benzyloxycarbonyl-, 2'-N-tert-butoxycarbonyl-, 6'-N-tert-butoxycarbonyl- and 2',6'-di-N-tert-butoxycarbonyl-fortimicin B (7, 8, 16, 18, 17) were prepared from 4. From these fortimicin B derivatives, selectively protected fortimicin A derivatives 13, 15, 21, 22 and 25 were prepared by combination of procedures of benzyloxycarbonylation or tert-butoxycarbonylation, 4-N-glycylation.lld:pubmed
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pubmed-article:7275833pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:7275833pubmed:articleTitleChemical modification of fortimicins. II. Selective protection of fortimicins A and B.lld:pubmed
pubmed-article:7275833pubmed:publicationTypeJournal Articlelld:pubmed