Synthesis, stereochemical assignment and biological activity of a novel series of C-4″ modified aza-Macrolides-Reference-Cited by-同舟云学术

Synthesis, stereochemical assignment and biological activity of a novel series of C-4″ modified aza-Macrolides

Published:2003-06 Issue:12 Volume:13 Page:1955-1958
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Bronk Brian S,Letavic Michael A,Bertsche Camilla D,George David M,Hayashi Shigeru F,Kamicker Barbara J,Kolosko Nicole L,Norcia Laura J,Rushing Margaret A,Santoro Sheryl L,Yang Bingwei V

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference5 articles.

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2. Synthesis, in vitro and in vivo activity of novel 9-deoxo-9a-aza-9a-homoerythromycin A derivatives; A new class of macrolide antibiotics, the azalides.

3. The synthesis of novel 8a-aza-8a-homoerythromycin derivatives via the beckmann rearrangement of (9z)-erythromycin a oxime

4. Preparation and activities of 4″-epi and 4″-deoxy-4″-amino analogs derived from 9-deoxo-8a-aza-8a-homoerythromycin A

5. Synthesis and Activity of a Novel Class of Tribasic Macrocyclic Antibiotics: The Triamilides

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