A Facile Fmoc Solid Phase Synthesis Strategy To Access Epimerization-Prone Biosynthetic Intermediates of Glycopeptide Antibiotics
Author:
Affiliation:
1. Department of Biomolecular Mechanisms, Max-Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany
Funder
Deutsche Forschungsgemeinschaft
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol500840f
Reference35 articles.
1. The Vancomycin Group of Antibiotics and the Fight against Resistant Bacteria
2. Total Synthesis of [Ψ[C(═S)NH]Tpg4]Vancomycin Aglycon, [Ψ[C(═NH)NH]Tpg4]Vancomycin Aglycon, and Related Key Compounds: Reengineering Vancomycin for Dual d-Ala-d-Ala and d-Ala-d-Lac Binding
3. Vancomycin, teicoplanin, and ramoplanin: Synthetic and mechanistic studies
4. Chemistry, Biology, and Medicine of the Glycopeptide Antibiotics
5. bWolter, F.; Schoof, S.; Süssmuth, R. D.InGlycopeptides and Glycoproteins;Wittmann, V., Ed.; Topics in Current Chemistry;Springer:Berlin, Heidelberg, 2007; pp143–185.
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