Preparation and antibacterial activity of cyclic 2′,3′-carbamate derivatives of azithromycin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Pharmacology,General Medicine
Reference19 articles.
1. Recent Developments on Ketolides and Macrolides
2. Structural basis for the interaction of antibiotics with the peptidyl transferase centre in eubacteria
3. Preparation of cyclic 2′,3′-carbamate derivatives of erythromycin macrolide antibiotics
4. Erythromycin series. Part 11. Ring expansion of erythromycin A oxime by the Beckmann rearrangement
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1. Synthesis and Antibacterial Evaluation of a Series of 11,12-Cyclic Carbonate Azithromycin-3-O-descladinosyl-3-O-carbamoyl Glycosyl Derivatives;Molecules;2017-12-04
2. Structure-Activity Relationships and Mechanism of Action of Macrolides Derived from Erythromycin as Antibacterial Agents;Current Topics in Medicinal Chemistry;2013-12-31
3. Synthesis and antibacterial activity of novel modified 5-O-mycaminose 14-membered ketolides;European Journal of Medicinal Chemistry;2013-11
4. Novel desosamine-modified 14- and 15-membered macrolides without antibacterial activity;Bioorganic & Medicinal Chemistry Letters;2012-05
5. Novel Tandem Reaction for the Synthesis of N′-Substituted 2-Imino-1,3-oxazolidines from Vicinal (sec- or tert-)Amino Alcohol of Desosamine;European Journal of Organic Chemistry;2011-03-15
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