A convenient synthesis of orthogonally protected 2-deoxystreptamine (2-DOS) as an aminocyclitol scaffold for the development of novel aminoglycoside antibiotic derivatives against bacterial resistance

标题
A convenient synthesis of orthogonally protected 2-deoxystreptamine (2-DOS) as an aminocyclitol scaffold for the development of novel aminoglycoside antibiotic derivatives against bacterial resistance
作者
关键词
-
出版物
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 6, Issue 16, Pages 2952
出版商
Royal Society of Chemistry (RSC)
发表日期
2008-06-20
DOI
10.1039/b804784g

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