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Volumn 6, Issue 16, 2008, Pages 2952-2960
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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
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Author keywords
[No Author keywords available]
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Indexed keywords
BACTERIOLOGY;
METAL DRAWING;
SYNTHESIS (CHEMICAL);
2-DEOXYSTREPTAMINE;
AMINOCYCLITOL;
AMINOGLYCOSIDE;
AMINOGLYCOSIDES;
BACTERIAL RESISTANCE;
CYCLOHEXANE RINGS;
ENANTIOPURE;
FACILE ACCESS;
FERRIER REARRANGEMENTS;
GLUCOPYRANOSIDE;
HYDRIDE REDUCTION;
SYNTHETIC APPROACHES;
HEALTH;
2 DEOXYSTREPTAMINE;
2-DEOXYSTREPTAMINE;
AMINOGLYCOSIDE;
ANTIINFECTIVE AGENT;
CYCLITOL;
HEXOSAMINE;
ANTIBIOTIC RESISTANCE;
ARTICLE;
CHEMICAL STRUCTURE;
CHEMISTRY;
OXIDATION REDUCTION REACTION;
STEREOISOMERISM;
SYNTHESIS;
AMINOGLYCOSIDES;
ANTI-BACTERIAL AGENTS;
CYCLITOLS;
DRUG RESISTANCE, MICROBIAL;
HEXOSAMINES;
MOLECULAR STRUCTURE;
OXIDATION-REDUCTION;
STEREOISOMERISM;
BACTERIA (MICROORGANISMS);
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EID: 49149121874
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/b804784g Document Type: Article |
Times cited : (15)
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References (98)
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