This mini-review provides an introduction to the key work in the area of synthesis and post-polymerization functionalization of maleimide-functional polymers. The versatility and utility of the maleimide group in the efficient functionalization of polymers by both 'thiol-ene' Michael addition and Diels-Alder cycloaddition chemistries are highlighted
A novel kinetic process was investigated for functionalizing "on-demand" local regions of well-defin...
This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36) and highlig...
A straightforward synthetic procedure for the double modification and polymer-polymer conjugation of...
We describe the synthesis of a thiolactone-functionalized maleimide (MITla), and its (co)polymerizat...
We show that many of the nucleophiles (catalysts, reducing agents, amines, thiols) present during “o...
We show that many of the nucleophiles (catalysts, reducing agents, amines, thiols) present during "o...
Diels-Alder chemistry is utilized for a myriad of commercial applications during polymer synthesis, ...
The stoichiometric reaction between thiols and maleimide-functional poly(ester)s is demonstrated to ...
A simple and economic two step synthesis of N‐alkylated maleimides with repeatable recycling of reco...
This work has investigated two routes of synthesising polymers containing L-histidine using maleimid...
The furan heterocycle is a dienic reagent particularly suitable for the Diels-Alder reaction and mal...
A series of a-functional maleimide polymethacrylates (M-n = 4.1-35.4 kDa, PDi = 1.06-1.27) have been...
This study concerns the synthesis and characterization of maleimide-based monomers and polymers. N-p...
The synthesis of functional polymers has been enriched dramatically by post-polymerization modificat...
ABSTRACT: Multiarm star polymers containing thiol-reactive maleimide groups at their core have been ...
A novel kinetic process was investigated for functionalizing "on-demand" local regions of well-defin...
This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36) and highlig...
A straightforward synthetic procedure for the double modification and polymer-polymer conjugation of...
We describe the synthesis of a thiolactone-functionalized maleimide (MITla), and its (co)polymerizat...
We show that many of the nucleophiles (catalysts, reducing agents, amines, thiols) present during “o...
We show that many of the nucleophiles (catalysts, reducing agents, amines, thiols) present during "o...
Diels-Alder chemistry is utilized for a myriad of commercial applications during polymer synthesis, ...
The stoichiometric reaction between thiols and maleimide-functional poly(ester)s is demonstrated to ...
A simple and economic two step synthesis of N‐alkylated maleimides with repeatable recycling of reco...
This work has investigated two routes of synthesising polymers containing L-histidine using maleimid...
The furan heterocycle is a dienic reagent particularly suitable for the Diels-Alder reaction and mal...
A series of a-functional maleimide polymethacrylates (M-n = 4.1-35.4 kDa, PDi = 1.06-1.27) have been...
This study concerns the synthesis and characterization of maleimide-based monomers and polymers. N-p...
The synthesis of functional polymers has been enriched dramatically by post-polymerization modificat...
ABSTRACT: Multiarm star polymers containing thiol-reactive maleimide groups at their core have been ...
A novel kinetic process was investigated for functionalizing "on-demand" local regions of well-defin...
This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36) and highlig...
A straightforward synthetic procedure for the double modification and polymer-polymer conjugation of...