The interface as a “screw clamp”: the copper-free 1,3-dipolar azide–alkyne cycloaddition at the interface of nanodroplets in miniemulsions was studied in detail by NMR spectroscopic methods. The reaction at the oil–water interface proved to exhibit higher rate constants, increased molecular weights and high regioregularity compared to the reaction in solutio
Protein-protein interactions are central to most biological processes. Although in the field of drug...
Here, we report a novel method to synthesize multifunctional nanoparticles that can be used in biolo...
Click chemistry is a molecular synthesis strategy based on reliable, highly selective reactions with...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Click reactions have provided access to an array of remarkably complex polymer architectures. Howeve...
Click reactions have provided access to an array of remarkably complex polymer architectures. Howeve...
Readily prepared copper nanoparticles were found to catalyse the 1,3-dipolar cycloaddition of azides...
The Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC, known as the click reaction) is an establishe...
The combination of highly efficient polymerizations with modular "click" coupling reactions has enab...
The alkyne-azide cycloaddition, popularly known as the "click" reaction, has been extensively exploi...
Bioorthogonal chemistries are reactions that are designed to proceed in living environments without ...
The reaction of triazolinediones (TADs) and indoles is of particular interest for polymer chemistry ...
With the goal of identifying alkyne-like reagents for use in click chemistry, but without Cu catalys...
The multivalent presentation of functional groups on nanoparticle surfaces has long been exploited t...
The first reported click reaction, copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition, had l...
Protein-protein interactions are central to most biological processes. Although in the field of drug...
Here, we report a novel method to synthesize multifunctional nanoparticles that can be used in biolo...
Click chemistry is a molecular synthesis strategy based on reliable, highly selective reactions with...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Click reactions have provided access to an array of remarkably complex polymer architectures. Howeve...
Click reactions have provided access to an array of remarkably complex polymer architectures. Howeve...
Readily prepared copper nanoparticles were found to catalyse the 1,3-dipolar cycloaddition of azides...
The Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC, known as the click reaction) is an establishe...
The combination of highly efficient polymerizations with modular "click" coupling reactions has enab...
The alkyne-azide cycloaddition, popularly known as the "click" reaction, has been extensively exploi...
Bioorthogonal chemistries are reactions that are designed to proceed in living environments without ...
The reaction of triazolinediones (TADs) and indoles is of particular interest for polymer chemistry ...
With the goal of identifying alkyne-like reagents for use in click chemistry, but without Cu catalys...
The multivalent presentation of functional groups on nanoparticle surfaces has long been exploited t...
The first reported click reaction, copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition, had l...
Protein-protein interactions are central to most biological processes. Although in the field of drug...
Here, we report a novel method to synthesize multifunctional nanoparticles that can be used in biolo...
Click chemistry is a molecular synthesis strategy based on reliable, highly selective reactions with...