Sequential thiol-ene/thiol-ene and thiol-ene/thiol-yne reactions as a route to well-defined mono and bis end-functionalized poly(N-isopropylacrylamide)
about
Exhaustive glycosylation, PEGylation, and glutathionylation of a [G4]-ene(48) dendrimer via photoinduced thiol-ene couplingPoly(allyl glycidyl ether)-A versatile and functional polyether platform.Selective and Quantitative Oxidation of Xanthate End-Groups of RAFT Poly(n-butyl acrylate) Latexes by Ozonolysis.Thiol-ene click chemistry.Combining RAFT radical polymerization and click/highly efficient coupling chemistries: a powerful strategy for the preparation of novel materials.RAFT polymerization and thiol chemistry: a complementary pairing for implementing modern macromolecular design."Clicking" on/with polymers: a rapidly expanding field for the straightforward preparation of novel macromolecular architectures.Recent applications of thiol-ene coupling as a click process for glycoconjugation.Click chemistry with polymers, dendrimers, and hydrogels for drug delivery.Selective Uptake of a Fructose Glycopolymer Prepared by RAFT Polymerization into Human Breast Cancer Cells.TBAI-Catalyzed/Water-Assisted Double C-S Bond Formations: An Efficient Approach to Sulfides through Metal-Free Three-Component Reactions.Combining ring-opening metathesis polymerization and thiol-ene coupling chemistries: facile access to novel functional linear and nonlinear macromolecules.Thiol-ene “click” reactions and recent applications in polymer and materials synthesisRAFT synthesis of triply responsive poly[N-[2-(dialkylamino)ethyl]acrylamide]s and their N-substitute determined responseHeterofunctional RAFT-derived PNIPAM via cascade trithiocarbonate removal and thiol-yne coupling click reactionThiol-ene Based Functionalization of PolymersNovel α,α-Bischolesteryl Functional (Co)Polymers: RAFT Radical Polymerization Synthesis and Preliminary Solution CharacterizationSynthesis of thermoresponsive oxazolone end-functional polymers for reactions with amines using thiol-Michael addition “click” chemistrytBCPMA: a new trifunctional acrylic monomer for convenient synthesis of a well-defined amphiphilic graft copolymer by successive RDRPPoly(N-isopropylacrylamide) hydrogels fabricated via click chemistry: well-defined α,ω-bis propargyl linear poly(N-isopropylacrylamide)s as crosslinkersN-Ester-substituted polyacrylamides with a tunable lower critical solution temperature (LCST): the N-ester-substitute dependent thermoresponseSynthesis and modification of thermoresponsive poly(oligo(ethylene glycol) methacrylate) via catalytic chain transfer polymerization and thiol–ene Michael additionPreparation of Well-Defined Propargyl-Terminated Tetra-Arm Poly(N-isopropylacrylamide)s and Their Click Hydrogels Crosslinked with β-cyclodextrinThermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation
P2860
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P2860
Sequential thiol-ene/thiol-ene and thiol-ene/thiol-yne reactions as a route to well-defined mono and bis end-functionalized poly(N-isopropylacrylamide)
description
im Juli 2009 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в липні 2009
@uk
name
Sequential thiol-ene/thiol-ene ...... nd bis end-functionalized poly
@nl
Sequential thiol-ene/thiol-ene ...... ed poly(N-isopropylacrylamide)
@en
type
label
Sequential thiol-ene/thiol-ene ...... nd bis end-functionalized poly
@nl
Sequential thiol-ene/thiol-ene ...... ed poly(N-isopropylacrylamide)
@en
prefLabel
Sequential thiol-ene/thiol-ene ...... nd bis end-functionalized poly
@nl
Sequential thiol-ene/thiol-ene ...... ed poly(N-isopropylacrylamide)
@en
P2093
P356
P1476
Sequential thiol-ene/thiol-ene ...... ed poly(N-isopropylacrylamide)
@en
P2093
Andrew B. Lowe
Charles E. Hoyle
Justin W. Chan
P304
P356
10.1002/POLA.23436
P577
2009-07-15T00:00:00Z