The first example of highly efficient sequential thiol-ene/thiol-yne reactions conducted in an orthogonal manner is presented and its broad application in the synthesis of polyfunctional materials demonstrated. The anionic chain mechanism of the phosphine-mediated thiol-ene reaction is highlighted, as is the radical-mediated thiol-yne reaction. Kinetic data for a model reaction are presented, followed by a discussion of the synthesis of a range of materials with diverse functionality, including an example of potential biomedical significance. © 2009 American Chemical Society
International audienceA series of alkene-functional polymers were synthesized by controlled polymeri...
The photopolymerization of mixtures of multifunctional thiols and enes is an efficient method for th...
The aim of this article is to highlight recent examples in which two powerful synthetic tools, namel...
The first example of highly efficient sequential thiol-ene/thiol-yne reactions conducted in an ortho...
Radical mediated thiol-yne polymerization reactions complement the more well-known thiol-ene radical...
This review is devoted to relatively new and promising approach to the synthesis of novel organic co...
This review highlights examples of recent applications of both the radical-mediated and base/nucleop...
ABSTRACT: Radical-mediated thiol-yne step-growth photopolymerizations are utilized to form highly cr...
The in situ generation of thiols by nucleophilic ring-opening of a thiolactone with amines, followed...
AbstractOne-pot multi-step reactions based on thiolactone chemistry emerged as a powerful tool to pr...
Radical-mediated thiol−yne step-growth photopolymerizations are utilized to form highly cross-linked...
This review highlights recent applications of the thiol-yne reaction in polymer synthesis and modifi...
Multifunctional alkynes (2, 3, or 4 ynes per monomer) were prepared utilizing the nucleophile-cataly...
This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36) and highlig...
The synthesis of 3-arm star polymers from reversible addition-fragmentation chain transfer (RAFT)-pr...
International audienceA series of alkene-functional polymers were synthesized by controlled polymeri...
The photopolymerization of mixtures of multifunctional thiols and enes is an efficient method for th...
The aim of this article is to highlight recent examples in which two powerful synthetic tools, namel...
The first example of highly efficient sequential thiol-ene/thiol-yne reactions conducted in an ortho...
Radical mediated thiol-yne polymerization reactions complement the more well-known thiol-ene radical...
This review is devoted to relatively new and promising approach to the synthesis of novel organic co...
This review highlights examples of recent applications of both the radical-mediated and base/nucleop...
ABSTRACT: Radical-mediated thiol-yne step-growth photopolymerizations are utilized to form highly cr...
The in situ generation of thiols by nucleophilic ring-opening of a thiolactone with amines, followed...
AbstractOne-pot multi-step reactions based on thiolactone chemistry emerged as a powerful tool to pr...
Radical-mediated thiol−yne step-growth photopolymerizations are utilized to form highly cross-linked...
This review highlights recent applications of the thiol-yne reaction in polymer synthesis and modifi...
Multifunctional alkynes (2, 3, or 4 ynes per monomer) were prepared utilizing the nucleophile-cataly...
This contribution serves as an update to a previous review (Polym. Chem. 2010, 1, 17–36) and highlig...
The synthesis of 3-arm star polymers from reversible addition-fragmentation chain transfer (RAFT)-pr...
International audienceA series of alkene-functional polymers were synthesized by controlled polymeri...
The photopolymerization of mixtures of multifunctional thiols and enes is an efficient method for th...
The aim of this article is to highlight recent examples in which two powerful synthetic tools, namel...