The combination of catalytic chain transfer polymerisation (CCTP) with both thiol-ene and copper catalysed alkyne azide coupling (CuAAC) click chemistry has been employed to give a new route to functional glycopolymers for applications in bioconjugation and biological targeting. Ring opening of poly(glycidyl methacrylate) with sodium azide and subsequent reaction with alkyne functional carbohydrates, as prepared by Fischer glycosylation, has been exploited. This combination of a range of efficient chemistry gives a route to multi gram quantities of glycopolymers avoiding the need for living radical polymerisation chemistry. © 2012 The Royal Society of Chemistry
Amphiphilic copolymers with pendant functional groups in polyester segments are widely used in nanom...
The objective of this thesis is to advance the development of catalytic chain transfer polymerizatio...
The copper catalyzed 1,3 dipolar "click" cycloaddition of azides and alkynes was used as a complemen...
CCTP has been used to give alkyne-functional macromonomers which are subsequently functionalised wit...
This mini-review describes recent work in the field of glycopolymer synthesis, with a focus on metho...
AbstractThis mini-review describes recent work in the field of glycopolymer synthesis, with a focus ...
The synthesis of novel well-defined alkyne side chain functional polymers featuring narrow molecular...
The combination of copper(0) mediated living radical polymerization (Cu(0)-LRP) with thiol–halogen, ...
The synthesis of polymers with latent reactivity suitable for ‘click’ type modifications in a tandem...
In the present thesis, well-defined complex polymeric architectures are realized via a combination o...
Synthetic glycopolypeptides have attracted much interest for application in biomedical field as they...
In this work, click chemistry was sucessfully applied to the chemical modification of aliphatic poly...
At the start of this research in 2006, the application of click chemistry on polymers was gaining a ...
The objective of the thesis was to prepare well-defined glycopolymers and glycoprotein mimics by com...
The bromine chain-ends of well-defined poly(oligo(ethylene glycol) acrylate) (POEGA) (M-n = 6850 g(....
Amphiphilic copolymers with pendant functional groups in polyester segments are widely used in nanom...
The objective of this thesis is to advance the development of catalytic chain transfer polymerizatio...
The copper catalyzed 1,3 dipolar "click" cycloaddition of azides and alkynes was used as a complemen...
CCTP has been used to give alkyne-functional macromonomers which are subsequently functionalised wit...
This mini-review describes recent work in the field of glycopolymer synthesis, with a focus on metho...
AbstractThis mini-review describes recent work in the field of glycopolymer synthesis, with a focus ...
The synthesis of novel well-defined alkyne side chain functional polymers featuring narrow molecular...
The combination of copper(0) mediated living radical polymerization (Cu(0)-LRP) with thiol–halogen, ...
The synthesis of polymers with latent reactivity suitable for ‘click’ type modifications in a tandem...
In the present thesis, well-defined complex polymeric architectures are realized via a combination o...
Synthetic glycopolypeptides have attracted much interest for application in biomedical field as they...
In this work, click chemistry was sucessfully applied to the chemical modification of aliphatic poly...
At the start of this research in 2006, the application of click chemistry on polymers was gaining a ...
The objective of the thesis was to prepare well-defined glycopolymers and glycoprotein mimics by com...
The bromine chain-ends of well-defined poly(oligo(ethylene glycol) acrylate) (POEGA) (M-n = 6850 g(....
Amphiphilic copolymers with pendant functional groups in polyester segments are widely used in nanom...
The objective of this thesis is to advance the development of catalytic chain transfer polymerizatio...
The copper catalyzed 1,3 dipolar "click" cycloaddition of azides and alkynes was used as a complemen...