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Proc. Natl. Acad. Sci. 2010, 107, 22528-22533
Perturbing the folding energy landscape of the bacterial immunity protein Im7 by site-specific N-linked glycosylation
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Chemical Science 2010, 1, 596-602
Site-specific PEGylation of proteins by a Staudinger-phosphite reaction
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Bioorg. Med. Chem. 2010, 18, 3679-3686
Acidic and basic deprotection strategies of borane-protected phosphinothioesters for the traceless Staudinger ligation
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J. Pep. Sci. 2010, 16, 563-567
Phosphoramidate-peptide synthesis by solution and solid-phase Staudinger-phosphite reactions
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Eur. J. Org. Chem. 2010, 26, 5004-5009
Solid-Phase Synthesis of Phosphoramidate-Linked Glycopeptides
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Chem. Commun. 2010, 46, 3080-3082
Enzymatically triggered amyloid formation: an approach for studying peptide aggregation
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Chem. Eur. J. 2010, 16, 7881-7888
How Post-Translational Modifications Influence Amyloid Formation: A Systematic Study of Phosphorylation and Glycosylation in Model Peptides
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Org. Biomol. Chem. 2010, 8, 2575-2579
Towards understanding secondary structure transitions: phosphorylation and metal coordination in model peptides
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Chem. Commun. 2010, 46, 3176-3178
Site-specific functionalisation of proteins by a Staudinger-type reaction using unsymmetrical phosphites
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in "Amino Acids, Peptides and Proteins in Organic Chemistry", Wiley-VCh, Andrew B. Huges (ed.) 2010, 445-494
Chemoselective Peptide Ligation - A Privileged Tool for Protein Synthesis (Book Chapter)
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ChemBioChem 2010, 11, 481-484
Chemically Tailored Multivalent Virus Platforms - From Drug Delivery to Catalysis (Highlight)
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ChemCatChem 2010, 2, 243-245
Suzuki-Miyaura Couplings on pProteins - a Simple and Ready-to-use Catalytic System in Water (Highlight)
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Chemie in unserer Zeit 2010, 44, 198-206
Semisynthese: Ein zentrales Werkzeug für die Chemische Biologie (Review)
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Chemie in unserer Zeit 2010, 44, 130-137
Semisynthese: Chemie mit den Molekülen der Natur (Review)
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Angew. Chem. Int. Ed. 2009, 48, 8234-8239
Chemoselective Staudinger-Phoshpite Reaction of Azides for the Phosphorylation of Proteins
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Angew. Chem. 2009, 121, 8382-8387
Chemoselektive Staudinger-Phosphit-Reaktion von Aziden für die Phosphorylierung von Proteinen
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Angew. Chem. Int. Ed. 2008, 47, 10030-10074
Chemoselective Ligation and Modification Strategies of Peptides and Proteins
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Angew. Chem. 2008, 120, 10182-10228
Chemoselektive Ligations- und Modifikationsstrategien für Peptide und Proteine
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Chem. Commun. 2008, 25, 2932-2934
Synthesis of N,N-disubstituted phosphoramidates via a Lewis acid-catalyzed phosphorimidate rearrangement
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Angew. Chem. Int. Ed. 2008, 47, 5984-5988
Chemoselective Peptide Cyclization by Traceless Staudinger Ligation
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Angew. Chem. 2008, 120, 6073-6078
Chemoselektive Peptidcyclisierung über spurlose Staudinger-Ligation
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ChemBioChem 2007, 8, 1763-1765
Chemoselective Labeling of Engineered Fucosylated Glycoproteins
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ChemBioChem 2007, 8, 1221-1223
A Synthetic Kiss of Death: Expressed Protein Ligation of a Ubiquitin-Peptide Conjugate
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Org. Biomol. Chem. 2006, 4, 2291-2295
The reduction of oxidized methionine residues in peptide thioesters with NH4I/Me2S
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Chemie in unserer Zeit (ChiuZ) 2006, 40, 174-183
Proteinstrukturen aus dem Chemie-Baukasten. Definierte Peptidarchitekturen
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Bioorg. Med. Chem. 2006, 14, 5043-5048
Expression of N-terminal Cys-protein fragments using an intein refolding strategy
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J. Am. Chem. Soc. 2005, 127, 12882-12889
Semisynthesis of a Glycosylated Im7 Analogue for Protein Folding Studies
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J. Org. Chem. 2005, 70, 3574-3578
Improving Glycopeptide Synthesis: A Convenient Protocol for the Preparation of ß-Glycosylamines and the Synthesis of Glycopeptides
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Adv. Synth. Catal. 2005, 347, 1696-1700
Ethylene-Bridged Bissulfoximines in Copper-Catalyzed Enantioselective Hetero-Diels-Alder Reactions
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Chem. Eur. J. 2004, 10, 2942-2952
Synthetic and Spectroscopic Investigation of N-Acylated Sulfoximines
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J. Org. Chem. 2004, 69, 739-743
General Synthesis of Unsymmetrical Norbornane Scaffolds as Inducers for Hydrogen Bond Interactions in Peptides
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Tetrahedron: Asymmetry 2003, 14, 3455-3467
An alkaloid-mediated desymmetrization of meso-anhydrides via a nucleophilic ring opening with benzyl alcohol and its application in the synthesis of highly enantiomerically enriched ß-amino acids
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Bioorg. Med. Chem. Lett. 2003, 13, 3207-3211
The stability of pseudopeptides bearing sulfoximines as chiral backbone modifying element towards proteinase K
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Synthesis 2002, 7, 879-887
N-Alkylation of Sulfoximines: A Mild Synthetic Procedure for the Introduction of Carbon Side-Chains via an Acylation and Reduction Route
Org. Lett. 2002, 4, 893-897
Turn Formation Initiated by a Bissulfoximine Motif: Synthesis and Structural Investigation
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Protein Sci. 2000, 9, 2518-2527
An improved tripod amphiphile for membrane protein solubilization
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