The 'sulfo-click' reaction, which is a chemoselective amidation reaction involving the reaction of an aminoethane sulfonyl azide with a thio acid, encompasses a new approach for ligation and conjugation. Detailed protocols are provided for decorating biologically active peptides or dendrimers with biophysical tags, fluorescent probes, metal chelators, and small peptides by using this reaction as a novel, metal-free 'sulfo-click' approach
Chemical ligation approaches have become essential tools for the engineering of complex molecules in...
A novel and selective tyrosine functionalization strategy through SuFEx (sulfur fluoride exchange) c...
Chemoselective ligations allow chemical biologists to functionalise proteins and peptides for biomed...
Chemical methods that enable the synthesis and the site-selective modification of biomolecules offer...
Ligation reactions have emerged as an important tool for the chemoselective conjugation of large and...
A highly efficient coupling of protected β-substituted aminoethane sulfonyl azides with thio acids i...
The first reported click reaction, copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition, had l...
The simple and fast CLICK reaction, in which an azide is linked to an alkyne, has been used extensiv...
This paper describes an optimized protocol for the efficient loading of resin-bound aminoethane sulf...
International audienceA novel homobifunctional cross-linker based on a bis-sultone benzenic scaffold...
A serine/threonine-based chemoselective ligation method is described. It uses an O-salicylaldehyde e...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
We describe a new bioconjugation reaction based on the aziridination of norbornenes using electron-d...
Peptides conjugated to labels as well as to other biomolecules are essential tools in biomedical res...
International audienceA novel strategy has been devised that allows a ligation of of thioacids and i...
Chemical ligation approaches have become essential tools for the engineering of complex molecules in...
A novel and selective tyrosine functionalization strategy through SuFEx (sulfur fluoride exchange) c...
Chemoselective ligations allow chemical biologists to functionalise proteins and peptides for biomed...
Chemical methods that enable the synthesis and the site-selective modification of biomolecules offer...
Ligation reactions have emerged as an important tool for the chemoselective conjugation of large and...
A highly efficient coupling of protected β-substituted aminoethane sulfonyl azides with thio acids i...
The first reported click reaction, copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition, had l...
The simple and fast CLICK reaction, in which an azide is linked to an alkyne, has been used extensiv...
This paper describes an optimized protocol for the efficient loading of resin-bound aminoethane sulf...
International audienceA novel homobifunctional cross-linker based on a bis-sultone benzenic scaffold...
A serine/threonine-based chemoselective ligation method is described. It uses an O-salicylaldehyde e...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
We describe a new bioconjugation reaction based on the aziridination of norbornenes using electron-d...
Peptides conjugated to labels as well as to other biomolecules are essential tools in biomedical res...
International audienceA novel strategy has been devised that allows a ligation of of thioacids and i...
Chemical ligation approaches have become essential tools for the engineering of complex molecules in...
A novel and selective tyrosine functionalization strategy through SuFEx (sulfur fluoride exchange) c...
Chemoselective ligations allow chemical biologists to functionalise proteins and peptides for biomed...