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Introducing the Azlactone Functionality into Polymers through Controlled Radical Polymerization: Strategies and Recent Developments
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Reactive poly(2-vinyl-4,4-dimethyl-5-oxazolone) and poly[(2-vinyl-4,4-dimethyl-5-oxazolone)-co-(methyl methacrylate)]s. Synthesis, characterization and chemical modification with 4-methoxy-4'-(β-aminoethoxy)biphenyl
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Click Chemistry: Diverse Chemical Function from a Few Good Reactions
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Synthesis of a Liquid Bisoxazolin-5-one by Radical Reaction of Bismercaptan onto 2-Ethenyloxazolin- 5-one
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Grafting of 2-vinyl-4,4-dimethylazlactone onto electron-beam activated poly(propylene) films and fabrics. Application to the immobilization of sericin
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The Emergence of Thiol–Ene Coupling as a Click Process for Materials and Bioorganic Chemistry
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“Clicking” Polymers or Just Efficient Linking: What Is the Difference?
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Photocrosslinked norbornene–thiol copolymers: Synthesis, mechanical properties, and cure studies
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Synthesis and Ring‐Opening Metathesis Polymerization (ROMP) Reactivity of endo‐and exo‐Norbornenylazlactone Using Ruthenium Catalysts
inferredcites →https://doi.org/10.1002/marc.200800416openalex-snapshot
Synthesis of Seven‐Arm Poly(vinyl pyrrolidone) Star Polymers with Lysozyme Core Prepared by MADIX/RAFT Polymerization
inferredcites →https://doi.org/10.1002/marc.201200063openalex-snapshot
Highly Efficient Ring‐Opening Reaction of Azlactone‐Based Copolymer Platforms for the Design of Functionalized Materials
inferredcites →https://doi.org/10.1002/masy.200750805openalex-snapshot
Substrate-Independent Stable and Adherent Reactive Surface Coatings and their Conversion with Amines
inferredcites →https://doi.org/10.1002/pola.10007openalex-snapshot
Chemistry and technology of 2‐alkenyl azlactones
inferredcites →https://doi.org/10.1002/pola.21644openalex-snapshot
Elaboration of well‐defined Rasta resins and their use as supported catalytic systems for atom transfer radical polymerization
inferredcites →https://doi.org/10.1002/pola.22117openalex-snapshot
Tuning the parameters of the suspension polymerization of styrene, divinylbenzene, and N‐(p‐vinylbenzyl)‐ 4,4‐dimethylazlactone
inferredcites →https://doi.org/10.1002/pola.22309openalex-snapshot
RAFT polymerization of a novel activated ester monomer and conversion to a terpyridine‐containing homopolymer
inferredcites →https://doi.org/10.1002/pola.22994openalex-snapshot
Synthesis of well‐defined polymeric activated esters
inferredcites →https://doi.org/10.1002/pola.24267openalex-snapshot
Facilitating polymer conjugation via combination of RAFT polymerization and activated ester chemistry
inferredcites →https://doi.org/10.1002/pola.24303openalex-snapshot
Block copolymers based on 2‐vinyl‐4,4‐dimethyl‐5‐oxazolone by RAFT polymerization: Experimental and computational studies
inferredcites →https://doi.org/10.1002/pola.25001openalex-snapshot
Synthesis and postfunctionalization of well‐defined star polymers via “double” click chemistry
inferredcites →https://doi.org/10.1016/0923-1137(92)90026-xopenalex-snapshot
Crosslinked, hydrophilic, azlactone-functional polymeric beads: A two-step approach
inferredcites →https://doi.org/10.1016/j.carres.2010.01.017openalex-snapshot
Solid-phase de novo synthesis of a (±)-2-deoxy-glycoside
inferredcites →https://doi.org/10.1016/j.eurpolymj.2004.05.005openalex-snapshot
Preparation and characterization of azlactone functionalized polymer supports and their application as scavengers
inferredcites →https://doi.org/10.1016/j.eurpolymj.2009.06.009openalex-snapshot
Shell-crosslinked nanoparticles through self-assembly of thermoresponsive block copolymers by RAFT polymerization
inferredcites →https://doi.org/10.1016/j.polymer.2011.11.021openalex-snapshot
Azlactone functionalization of magnetic nanoparticles using ATRP and their bioconjugation
inferredcites →https://doi.org/10.1016/j.progpolymsci.2006.11.002openalex-snapshot
Controlled/living radical polymerization: Features, developments, and perspectives
inferredcites →https://doi.org/10.1016/j.progpolymsci.2007.07.005openalex-snapshot
Modern trends in polymer bioconjugates design
inferredcites →https://doi.org/10.1016/j.reactfunctpolym.2007.10.008openalex-snapshot
New functionalized polyHIPE materials used as amine scavengers in batch and flow-through processes
inferredcites →https://doi.org/10.1016/s1381-1169(02)00229-7openalex-snapshot
Ring-opening metathesis polymerization (ROMP) of isomerically pure functional monomers and acyclic diene metathesis depolymerization (retro-ADMET) of functionalized polyalkenamers
inferredcites →https://doi.org/10.1021/bm200469aopenalex-snapshot
Side-Chain Peptide-Synthetic Polymer Conjugates via Tandem “Ester-Amide/Thiol–Ene” Post-Polymerization Modification of Poly(pentafluorophenyl methacrylate) Obtained Using ATRP
inferredcites →https://doi.org/10.1021/bm7013476openalex-snapshot
Efficient Catalytic Synthesis of Dendritic Polymers Having Internal Fluorescence Labels for Bioconjugation
inferredcites →https://doi.org/10.1021/bm8006715openalex-snapshot
End-Functionalized Phosphorylcholine Methacrylates and their Use in Protein Conjugation
inferredcites →https://doi.org/10.1021/bm901095jopenalex-snapshot
Synthesis of Hetero-Telechelic α,ω Bio-Functionalized Polymers
inferredcites →https://doi.org/10.1021/cc0600122openalex-snapshot
Well-Defined Azlactone-Functionalized (Co)polymers on a Solid Support: Synthesis via Supported Living Radical Polymerization and Application as Nucleophile Scavengers
inferredcites →https://doi.org/10.1021/cr9001403openalex-snapshot
Bioapplications of RAFT Polymerization
inferredcites →https://doi.org/10.1021/cr990119uopenalex-snapshot
New Polymer Synthesis by Nitroxide Mediated Living Radical Polymerizations
inferredcites →https://doi.org/10.1021/ja057481copenalex-snapshot
Versatile Precursors of Functional RAFT Agents. Application to the Synthesis of Bio-Related End-Functionalized Polymers
inferredcites →https://doi.org/10.1021/la904111ropenalex-snapshot
Molecular Recognition at the Exterior Surface of a Zwitterionic Telomer Brush
inferredcites →https://doi.org/10.1021/ma025817mopenalex-snapshot
Synthesis of Reactive Poly(vinyl oxazolones) via Nitroxide-Mediated “Living” Free Radical Polymerization
inferredcites →https://doi.org/10.1021/ma035012uopenalex-snapshot
Copper-Mediated Living Radical Polymerization of 2-Vinyl-4,4-dimethyl-5-oxazolone
inferredcites →https://doi.org/10.1021/ma201085zopenalex-snapshot
Acid Degradable and Biocompatible Polymeric Nanoparticles for the Potential Codelivery of Therapeutic Agents
inferredcites →https://doi.org/10.1021/ma202700yopenalex-snapshot
Synthesis and Thermoresponsive Solution Properties of Poly[oligo(ethylene glycol) (meth)acrylamide]s: Biocompatible PEG Analogues
inferredcites →https://doi.org/10.1021/ma900417nopenalex-snapshot
A Versatile Grafting-to Approach for the Bioconjugation of Polymers to Collagen-like Peptides Using an Activated Ester Chain Transfer Agent
inferredcites →https://doi.org/10.1021/ma9015399openalex-snapshot
Dilute Solution Properties and Surface Attachment of RAFT Polymerized 2-Vinyl-4,4-dimethyl Azlactone (VDMA)
inferredcites →https://doi.org/10.1021/ma902391bopenalex-snapshot
Synthesis of Heterotelechelic α,ω Dye-Functionalized Polymer by the RAFT Process and Energy Transfer between the End Groups
inferredcites →https://doi.org/10.1021/ma980240nopenalex-snapshot
Controlled Graft Polymerization of Methyl Methacrylate on Silicon Substrate by the Combined Use of the Langmuir−Blodgett and Atom Transfer Radical Polymerization Techniques
inferredcites →https://doi.org/10.1021/ma9804951openalex-snapshot
Living Free-Radical Polymerization by Reversible Addition−Fragmentation Chain Transfer: The RAFT Process
inferredcites →https://doi.org/10.1021/ma990175xopenalex-snapshot
Atom Transfer Radical Polymerization of (Meth)acrylamides
inferredcites →https://doi.org/10.1021/ma991146popenalex-snapshot
Polymers at Interfaces: Using Atom Transfer Radical Polymerization in the Controlled Growth of Homopolymers and Block Copolymers from Silicon Surfaces in the Absence of Untethered Sacrificial Initiator
inferredcites →https://doi.org/10.1039/b910296eopenalex-snapshot
One- pot synthesis and biofunctionalization of glycopolymers via RAFT polymerization and thiol–ene reactions
inferredcites →https://doi.org/10.1039/b9py00216bopenalex-snapshot
Thiol-ene “click” reactions and recent applications in polymer and materials synthesis
inferredcites →https://doi.org/10.1039/b9py00363kopenalex-snapshot
Recent advances in the design of bioconjugates from controlled/living radical polymerization
inferredcites →https://doi.org/10.1039/c0cc04062bopenalex-snapshot
Emerging synthetic approaches for protein–polymer conjugations
inferredcites →https://doi.org/10.1039/c0py00100gopenalex-snapshot
Investigation into thiol-(meth)acrylate Michael addition reactions using amine and phosphine catalysts
inferredcites →https://doi.org/10.1039/c0py00178copenalex-snapshot
Protein conjugation of thermoresponsive amine-reactive polymers prepared by RAFT
inferredcites →https://doi.org/10.1039/c0sm00412jopenalex-snapshot
An overview of protein–polymer particles
inferredcites →https://doi.org/10.1039/c1py00028dopenalex-snapshot
First peptide/protein PEGylation with functional polymers designed by nitroxide-mediated polymerization
inferredcites →https://doi.org/10.1039/c1py00071copenalex-snapshot
Synthesis of thermoresponsive oxazolone end-functional polymers for reactions with amines using thiol-Michael addition “click” chemistry
inferredcites →https://doi.org/10.1039/c1py00314copenalex-snapshot
Azlactone-functionalized polymers as reactive platforms for the design of advanced materials: Progress in the last ten years
inferredcites →https://doi.org/10.1039/c1py00320hopenalex-snapshot
Stable azlactone-functionalized nanoparticles prepared from thermoresponsive copolymers synthesized by RAFT polymerization
inferredcites →https://doi.org/10.1071/ch06250openalex-snapshot
Living Radical Polymerization by the RAFT Process—A First Update
inferredcites →https://doi.org/10.1071/ch09311openalex-snapshot
Living Radical Polymerization by the RAFT Process – A Second Update
inferredcites →https://doi.org/10.1071/ch12295openalex-snapshot
Living Radical Polymerization by the RAFT Process – A Third Update
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4680415openalex-extracted
Photo-Controlled Organocatalyzed Radical Polymerization Synthesis of Well-Defined Azlactone-Functionalized Polymers and its (Bio)Conjugated Application
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Functional Polymer Surfaces via Post‐polymerization Modification
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Synthesis and Applications of Protein/Peptide-Polymer Conjugates
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Fabrication, chemical modification, and topographical patterning of reactive gels assembled from azlactone‐functionalized polymers and a diamine
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One-Pot Double Modification of Polymers Based on Thiolactone Chemistry
inferred← citeshttps://doi.org/10.1007/978-3-319-92067-2_2-1openalex-snapshot
Polymer Functionalization
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Polymer Functionalization
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Polymer Analogous Reactions
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First investigation of modified poly(2-vinyl-4,4-dimethylazlactone)s as kinetic hydrate inhibitors
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Factors influencing the synthesis and the post-modification of PEGylated pentafluorophenyl acrylate containing copolymers
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One-pot multi-step reactions based on thiolactone chemistry: A powerful synthetic tool in polymer science
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Poly(norbornenyl azlactone) as a versatile platform for sequential double click postpolymerization modification
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2022.111310openalex-snapshot
Synthesis of a dual UCST-type thermosensitive and acid-degradable nanogel based on poly(N-acryloyl glycinamide) and a ketal-containing crosslinker
inferred← citeshttps://doi.org/10.1016/j.msec.2016.05.032openalex-snapshot
Recyclable magnetic nanocluster crosslinked with poly(ethylene oxide)-block-poly(2-vinyl-4,4-dimethylazlactone) copolymer for adsorption with antibody
inferred← citeshttps://doi.org/10.1016/j.polymer.2024.127251openalex-snapshot
Photo-controlled organocatalyzed radical polymerization synthesis of well-defined azlactone-functionalized polymers and its (bio)conjugated application
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.9b00155openalex-snapshot
Protein–Polymer Conjugates Synthesized Using Water-Soluble Azlactone-Functionalized Polymers Enable Receptor-Specific Cellular Uptake toward Targeted Drug Delivery
inferred← citeshttps://doi.org/10.1021/acs.biomac.3c00406openalex-snapshot
ROMP-based Glycopolymers with High Affinity for Mannose-Binding Lectins
inferred← citeshttps://doi.org/10.1021/acs.biomac.5b01682openalex-snapshot
Peptide Conjugation to a Polymer Coating via Native Chemical Ligation of Azlactones for Cell Culture
inferred← citeshttps://doi.org/10.1021/acs.biomac.6b00975openalex-snapshot
Degradable Amine-Reactive Coatings Fabricated by the Covalent Layer-by-Layer Assembly of Poly(2-vinyl-4,4-dimethylazlactone) with Degradable Polyamine Building Blocks
inferred← citeshttps://doi.org/10.1021/acs.chemmater.6b01897openalex-snapshot
Covalently Crosslinked and Physically Stable Polymer Coatings with Chemically Labile and Dynamic Surface Features Fabricated by Treatment of Azlactone-Containing Multilayers with Alcohol-, Thiol-, and Hydrazine-Based Nucleophiles
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A Versatile Cyclic Clickable Platform by Ring-Expansion Metathesis Polymerization: Cyclic Glycopolymers with Lectin-Binding Ability
inferred← citeshttps://doi.org/10.1021/acs.macromol.5b00178openalex-snapshot
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Synthesis, Characterization, and Polymerization of 4′-Acyl(oxy) Alkenyl Azlactone Monomers Designed Using a Steglich Rearrangement Approach
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Self-Assembly and Post-Fabrication Functionalization of Microphase Separated Thin Films of a Reactive Azlactone-Containing Block Copolymer
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Thiolactone-Functional Reversible Deactivation Radical Polymerization Agents for Advanced Macromolecular Engineering
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Thermoresponsive block copolymers containing reactive azlactone groups and their bioconjugation with lysozyme
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