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Synthesis of bicyclic tripeptides inspired by the ABC-ring system of vancomycin through ruthenium-based cyclization chemistries
Authors:Xin Yang  Lucas P. Beroske  Johan Kemmink  Dirk T.S. Rijkers  Rob M.J. Liskamp
Affiliation:1. Division of Chemical Biology & Drug Discovery, Utrecht Institute for Pharmaceutical Sciences, Department of Pharmaceutical Sciences, Faculty of Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands;2. School of Chemistry, University of Glasgow, Joseph Black Building, University Avenue, Glasgow G12 8QQ, United Kingdom
Abstract:The synthesis of a bicyclic tripeptide that mimics the ABC ring system of vancomycin is described by using a ring closing metathesis (RCM) – peptide coupling – ruthenium-catalyzed azide-alkyne cycloaddition (RuAAC) strategy.
Keywords:Macrocycles  Peptides  Peptidomimetics  Ring-closing metathesis  Ru-based azide-alkyne cycloaddition
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