1978Bulletin of the Chemical Society of JapanRequires access

Modification of Aminocyclitol Antibiotics. 6. Preparation of 5-Deoxykanamycin B

Tetsuo Suami, Shigeru Nishiyama, Yasuhide Ishikawa, Eijiro Umemura

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Abstract

Abstract Aminocyclitol antibiotic kanamycin B has been modified as regards the aminocyclitol moiety by removing a hydroxyl group on C-5. 5-Deoxykanamycin B thus obtained was tested against several microorganisms. The structure of 5-deoxykanamycin B was established by mass and 13C NMR spectrometry. 5,6,3′,4′-Tetradeoxyneamine was prepared as a reference compound for 13C NMR spectrometry.

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Abstract Aminocyclitol antibiotic kanamycin B has been modified as regards the aminocyclitol moiety by removing a hydroxyl group on C-5. 5-Deoxykanamycin B thus obtained was tested against several microorganisms. The structure of 5-deoxykanamycin B was established by mass and 13C NMR spectrometry. 5,6,3′,4′-Tetradeoxyneamine was prepared as a reference compound for 13C NMR spectrometry.

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Available abstract

Abstract Aminocyclitol antibiotic kanamycin B has been modified as regards the aminocyclitol moiety by removing a hydroxyl group on C-5. 5-Deoxykanamycin B thus obtained was tested against several microorganisms. The structure of 5-deoxykanamycin B was established by mass and 13C NMR spectrometry. 5,6,3′,4′-Tetradeoxyneamine was prepared as a reference compound for 13C NMR spectrometry.

Key concepts: Aminocyclitol, Chemistry, Kanamycin, Moiety, Mass spectrometry, Antibiotics, Stereochemistry, Aminoglycoside

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