AbstractOne-pot multi-step reactions based on thiolactone chemistry emerged as a powerful tool to prepare tailor-made, multi-functionalized polymer architectures in a one-pot and elegant manner. This feature article highlights the most important features of this approach, demonstrated in various reactive systems including (bio-based) linear polymers, heterotelechelic polymers, polymeric networks and heterogeneous supports. This overview clearly reveals its remarkable versatility involving modular synthesis and double modification of polymers: thiolactones can be opened by a wide variety of functional amines and the released thiol can react with thiol ‘scavengers’ of choice
The aim of this research project was to develop a method for the synthesis of advanced polymeric str...
The merits of thiol-click chemistry and its potential for making new forays into chemical synthesis ...
The merits of thiol-click chemistry and its potential for making new forays into chemical synthesis ...
One-pot multistep reactions based on thiolactone chemistry have emerged as a powerful tool for modif...
One-pot multistep reactions based on thiolactone chemistry have emerged as a powerful tool for modif...
The in situ generation of thiols by nucleophilic ring-opening of a thiolactone with amines, followed...
The in situ generation of thiols by nucleophilic ring-opening of a thiolactone with amines, followed...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
A series of thiol-based 'click' reactions is discussed with an emphasis on highlighting the individu...
This review highlights examples of recent applications of both the radical-mediated and base/nucleop...
This review is devoted to relatively new and promising approach to the synthesis of novel organic co...
This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36) and highlig...
The development of innovative, easy to implement strategies for polymer synthesis and modification c...
The aim of this research project was to develop a method for the synthesis of advanced polymeric str...
The merits of thiol-click chemistry and its potential for making new forays into chemical synthesis ...
The merits of thiol-click chemistry and its potential for making new forays into chemical synthesis ...
One-pot multistep reactions based on thiolactone chemistry have emerged as a powerful tool for modif...
One-pot multistep reactions based on thiolactone chemistry have emerged as a powerful tool for modif...
The in situ generation of thiols by nucleophilic ring-opening of a thiolactone with amines, followed...
The in situ generation of thiols by nucleophilic ring-opening of a thiolactone with amines, followed...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
A conceptual proof for the double modification (aminolysis and subsequent thiol-click modification) ...
A series of thiol-based 'click' reactions is discussed with an emphasis on highlighting the individu...
This review highlights examples of recent applications of both the radical-mediated and base/nucleop...
This review is devoted to relatively new and promising approach to the synthesis of novel organic co...
This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36) and highlig...
The development of innovative, easy to implement strategies for polymer synthesis and modification c...
The aim of this research project was to develop a method for the synthesis of advanced polymeric str...
The merits of thiol-click chemistry and its potential for making new forays into chemical synthesis ...
The merits of thiol-click chemistry and its potential for making new forays into chemical synthesis ...