This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36)
and highlights recent applications of thiol–ene 'click'chemistry as an efficient tool for both …

This review highlights recent applications of the thiol-yne reaction in polymer synthesis and
modification and also gives some representative examples of its application in small …

The key attribute of the thiol-Michael addition reaction that makes it a prized tool in materials
science is its modular “click” nature, which allows for the implementation of this highly …

Despite originating only a little more than a decade ago, click chemistry has become one of
the most powerful paradigms in materials science, synthesis, and modification. By …

The mechanism and kinetics of thiol–maleimide “click” reactions carried out under a variety
of conditions have been investigated computationally and using experimental competition …

Acrylate chemistry has found widespread use in dual-curing systems over the years.
Acrylates are cheap, easily handled and versatile monomers that can undergo facile chain …

A carbene-catalyzed asymmetric access to chiral β-cyano carboxylic esters is disclosed. The
reaction proceeds between β, β-disubstituted enals and aromatic thiols involving …

Photochemical processes enable spatial and temporal control of reactions, which can be
implemented as an accurate external control approach in both polymer synthesis and …

The thia‐Michael addition reaction has been demonstrated to be a highly powerful tool in
organic synthesis. Indeed, the influential nature of this reaction has been well‐established in …

The reactivity, selectivity and kinetics of vinyl sulfones and acrylates in base and nucleophile-
catalyzed thiol–Michael addition reactions were examined in detail in this study. The vinyl …