One-Pot Approach to Well-Defined Biomolecular Assemblies by Orthogonal Chemoselective Ligations

Click-click cyclopeptides: Well-defined biomolecular assemblies are synthesized using orthogonal oxime bond formation and copper(I)-mediated alkyne-azide cycloaddition reactions in a stepwise or in a one-pot approach. To illustrate this strategy, regioselective ligation of biologically relevant pept...

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Veröffentlicht in:Angewandte Chemie (International ed.) 2009-03, Vol.48 (14), p.2576-2579
Hauptverfasser: Galibert, Mathieu, Dumy, Pascal, Boturyn, Didier
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container_title Angewandte Chemie (International ed.)
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creator Galibert, Mathieu
Dumy, Pascal
Boturyn, Didier
description Click-click cyclopeptides: Well-defined biomolecular assemblies are synthesized using orthogonal oxime bond formation and copper(I)-mediated alkyne-azide cycloaddition reactions in a stepwise or in a one-pot approach. To illustrate this strategy, regioselective ligation of biologically relevant peptides onto a cyclopeptidic scaffold was performed.
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Alkynes - chemistry
Azides - chemistry
Catalysis
Chemical Sciences
chemoselectivity
click chemistry
copper
Copper - chemistry
Cyclization
oximes
Oximes - chemistry
peptides
Peptides - chemical synthesis
Peptides - chemistry
Peptides, Cyclic - chemical synthesis
Peptides, Cyclic - chemistry
title One-Pot Approach to Well-Defined Biomolecular Assemblies by Orthogonal Chemoselective Ligations
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