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Copper-Mediated Living Radical Polymerization of 2-Vinyl-4,4-dimethyl-5-oxazolone

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1521-4095(199808)10:12<901::aid-adma901>3.0.co;2-bopenalex-snapshot
Atom Transfer Radical Polymerization and the Synthesis of Polymeric Materials
inferredcites →https://doi.org/10.1002/1521-3935(200207)203:10/11<1377::aid-macp1377>3.0.co;2-nopenalex-snapshot
Grafting of 2-vinyl-4,4-dimethylazlactone onto electron-beam activated poly(propylene) films and fabrics. Application to the immobilization of sericin
inferredcites →https://doi.org/10.1002/9780470132333.ch2openalex-snapshot
Silver Chlorate
inferredcites →https://doi.org/10.1002/marc.1982.030031105openalex-snapshot
Synthesis of poly(4,4‐dimethyl‐2‐vinyl‐5‐oxazolone) an interesting material for preparing polymeric agents
inferredcites →https://doi.org/10.1002/marc.200290002openalex-snapshot
Xanthates as Chain‐Transfer Agents in Controlled Radical Polymerization (MADIX): Structural Effect of the O‐Alkyl Group
inferredcites →https://doi.org/10.1002/pol.1969.110070807openalex-snapshot
The synthesis of vinyl peptide monomers
inferredcites →https://doi.org/10.1016/0010-8545(91)80026-aopenalex-snapshot
Metals and ligand reactivity
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/s0079-6700(01)00003-xopenalex-snapshot
Functional polymers by atom transfer radical polymerization
inferredcites →https://doi.org/10.1016/s1369-7021(05)00745-5openalex-snapshot
Controlled/living radical polymerization
inferredcites →https://doi.org/10.1021/bk-1998-0685.ch016openalex-snapshot
Mechanistic Aspects of Atom Transfer Radical Polymerization
inferredcites →https://doi.org/10.1021/cr940534gopenalex-snapshot
Atom Transfer Radical Polymerization
inferredcites →https://doi.org/10.1021/ma000871topenalex-snapshot
Optimization of Atom Transfer Radical Polymerization Using Cu(I)/Tris(2-(dimethylamino)ethyl)amine as a Catalyst
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/ma9517310openalex-snapshot
Highly Cross-Linked Azlactone Functional Supports of Tailorable Polarity
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

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Photo-Controlled Organocatalyzed Radical Polymerization Synthesis of Well-Defined Azlactone-Functionalized Polymers and its (Bio)Conjugated Application
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Polymers Bearing Reactive, Pendant Cyclic Carbonate (CC) Group: Syntheses, Post‐Polymerization Modifications, and Applications
inferred← citeshttps://doi.org/10.1002/9781118870068.ch12openalex-snapshot
Polymer–Protein/Peptide Bioconjugates
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Layer‐by‐Layer Fabrication of Covalently Crosslinked and Reactive Polymer Multilayers Using Azlactone‐Functionalized Copolymers: A Platform for the Design of Functional Biointerfaces
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Synthese funktioneller Polymere durch polymeranaloge Reaktionen
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Synthesis of Functional Polymers by Post‐Polymerization Modification
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N‐Chlorosuccinimide (NCS): A Novel Initiator for Atom Transfer Radical Polymerization of Methyl Methacrylate†
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In Situ Polymer Analogue Generation of Azlactone Functions at Poly(oxazoline)s for Peptide Conjugation
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Highly Efficient Ring‐Opening Reaction of Azlactone‐Based Copolymer Platforms for the Design of Functionalized Materials
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Amine‐Reactive Polymers Synthesized by RAFT Polymerization Using an Azlactone Functional Trithiocarbonate RAFT Agent
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Molecular design of polymer coatings capable of photo‐triggered stress relaxation via dynamic covalent bond exchange
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Well‐defined polymers with acetal side chains as reactive scaffolds synthesized by atom transfer radical polymerization
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Elaboration of well‐defined Rasta resins and their use as supported catalytic systems for atom transfer radical polymerization
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Sequential conversion of orthogonally functionalized diblock copolymers based on pentafluorophenyl esters
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/pola.26281openalex-snapshot
Synthesis and properties of water‐soluble azlactone copolymers
inferred← citeshttps://doi.org/10.1016/b978-0-08-055294-1.00266-xopenalex-snapshot
Polymeric Drug Conjugates by Controlled Radical Polymerization
inferred← citeshttps://doi.org/10.1016/b978-0-08-100691-7.00020-3openalex-snapshot
4.27 Polymeric Drug Conjugates by Controlled Radical Polymerization
inferred← citeshttps://doi.org/10.1016/b978-0-12-803581-8.01420-xopenalex-snapshot
Polymer Analogous Reactions
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Post-Polymerization Modification
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Azlactone-functionalized smart block copolymers for organocatalyst immobilization
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Synthesis of mechanically robust renewable poly(ester-amide)s through co-polymerisation of unsaturated polyesters and synthetic polypeptides
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Well-defined polymers with activated ester and protected aldehyde side chains for bio-functionalization
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Controllable synthesis of poly(N-vinylpyrrolidone) and its block copolymers by atom transfer radical polymerization
inferred← citeshttps://doi.org/10.1016/j.polymer.2011.11.021openalex-snapshot
Azlactone functionalization of magnetic nanoparticles using ATRP and their bioconjugation
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.macromol.5c01040openalex-snapshot
Synthesis, Characterization, and Polymerization of 4′-Acyl(oxy) Alkenyl Azlactone Monomers Designed Using a Steglich Rearrangement Approach
inferred← citeshttps://doi.org/10.1021/acs.macromol.6b01212openalex-snapshot
Synthesis and Characterization of Backbone Degradable Azlactone-Functionalized Polymers
inferred← citeshttps://doi.org/10.1021/acs.macromol.6b01734openalex-snapshot
Self-Assembly and Post-Fabrication Functionalization of Microphase Separated Thin Films of a Reactive Azlactone-Containing Block Copolymer
inferred← citeshttps://doi.org/10.1021/acs.macromol.7b00465openalex-snapshot
50th Anniversary Perspective: Polymer Functionalization
inferred← citeshttps://doi.org/10.1021/acs.macromol.9b00352openalex-snapshot
Removable Nonconjugated Polymers To Debundle and Disperse Carbon Nanotubes
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/cr900234bopenalex-snapshot
Transition Metal-Catalyzed Living Radical Polymerization: Toward Perfection in Catalysis and Precision Polymer Synthesis
inferred← citeshttps://doi.org/10.1021/ja058743dopenalex-snapshot
Rapid Growth of Polymer Brushes from Immobilized Initiators
inferred← citeshttps://doi.org/10.1021/la8024952openalex-snapshot
Surface-Anchored Poly(2-vinyl-4,4-dimethyl azlactone) Brushes as Templates for Enzyme Immobilization
inferred← citeshttps://doi.org/10.1021/la802925gopenalex-snapshot
Immobilization of Biomolecules on Poly(vinyldimethylazlactone)-Containing Surface Scaffolds
inferred← citeshttps://doi.org/10.1021/la902553fopenalex-snapshot
High Density Scaffolding of Functional Polymer Brushes: Surface Initiated Atom Transfer Radical Polymerization of Active Esters
inferred← citeshttps://doi.org/10.1021/ma302183gopenalex-snapshot
Keto-Functionalized Polymer Scaffolds as Versatile Precursors to Polymer Side-Chain Conjugates
inferred← citeshttps://doi.org/10.1021/ma801681bopenalex-snapshot
Synthesis of Reactive Telechelic Polymers Based on Pentafluorophenyl Esters
inferred← citeshttps://doi.org/10.1021/ma900316topenalex-snapshot
Highly Tailorable Materials based on 2-Vinyl-4,4-dimethyl Azlactone: (Co)Polymerization, Synthetic Manipulation and Characterization
inferred← citeshttps://doi.org/10.1021/ma9015399openalex-snapshot
Dilute Solution Properties and Surface Attachment of RAFT Polymerized 2-Vinyl-4,4-dimethyl Azlactone (VDMA)
inferred← citeshttps://doi.org/10.1021/mz500654aopenalex-snapshot
Post-Fabrication Placement of Arbitrary Chemical Functionality on Microphase-Separated Thin Films of Amine-Reactive Block Copolymers
inferred← citeshttps://doi.org/10.1039/b921664bopenalex-snapshot
Azlactone-functionalized polymers as reactive templates for parallel polymer synthesis: synthesis and screening of a small library of cationic polymers in the context of DNA delivery
inferred← citeshttps://doi.org/10.1039/c0jm02633fopenalex-snapshot
Fabrication of covalently crosslinked and amine-reactive microcapsules by reactive layer-by-layer assembly of azlactone-containing polymer multilayers on sacrificial microparticle templates
inferred← citeshttps://doi.org/10.1039/c1py00071copenalex-snapshot
Synthesis of thermoresponsive oxazolone end-functional polymers for reactions with amines using thiol-Michael addition “click” chemistry
inferred← citeshttps://doi.org/10.1039/c1py00314copenalex-snapshot
Azlactone-functionalized polymers as reactive platforms for the design of advanced materials: Progress in the last ten years
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Thermoresponsive block copolymers containing reactive azlactone groups and their bioconjugation with lysozyme
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Poly(azlactone)s: versatile scaffolds for tandem post-polymerisation modification and glycopolymer synthesis
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An optimised Cu(0)-RDRP approach for the synthesis of lipidated oligomeric vinyl azlactone: toward a versatile antimicrobial materials screening platform
inferred← citeshttps://doi.org/10.1039/d4py00070fopenalex-snapshot
Azlactone-based copolymers by redox-initiated MADIX polymerization at room temperature in ethanol
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Introducing the Azlactone Functionality into Polymers through Controlled Radical Polymerization: Strategies and Recent Developments
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Micellar Organocatalysis Using Smart Polymer Supports: Influence of Thermoresponsive Self-Assembly on Catalytic Activity
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Azlactome funchionalization of magnetic nanoparticles using CRP techniques and their bioconjugation
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Mécanismes élémentaires de plasticité des systèmes polymères amorphes : influence de la modification de la structure macromoléculaire par la chimie « Click »
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