Synthesis of 2″-acylamido derivatives of 2″-amino-5,2″-dideoxy-5-epi-5-fluorodibekacin and a study on the structures of 5-fluorinated dibekacin analogs by 13C NMR-Reference-Cited by-同舟云学术

Synthesis of 2″-acylamido derivatives of 2″-amino-5,2″-dideoxy-5-epi-5-fluorodibekacin and a study on the structures of 5-fluorinated dibekacin analogs by 13C NMR

Published:1997-04 Issue:4 Volume:299 Page:271-279
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Kuwahara Ryuji,Tsuchiya Tsutomu

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference26 articles.

1. 3'', 4''-DIDEOXY-KANAMYCIN B ACTIVE AGAINST KANAMYCIN-RESISTANT ESCHERICHIA COLI AND PSEUDOMONAS AERUGINOSA

2. Studies on Aminosugars. XXXII. Synthesis of 3′, 4′-Dideoxykanamycin B

3. SYNTHESES OF 1-N-{(S)-4-AMINO-2-HYDROXYBUTYRYL}-KANAMYCIN B AND -3'', 4''-DIDEOXYKANAMYCIN B ACTIVE AGAINST KANAMYCIN-RESISTANT BACTERIA

4. Structures of enzymatically modified products of arbekacin by methicillin-resistant Staphylococcus aureus.

5. Synthesis of kanamycin a analogs containing 6-amino-3-oxa-2,3,4,6-tetradeoxy-d- and -l-glycero-hexopyranose

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