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Well-defined amine-reactive polymethacrylates through organocatalyzed controlled radical polymerization

https://doi.org/10.1039/d2py00873d
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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/anie.201710964openalex-snapshot
Temperature‐Selective Dual Radical Generation from Alkyl Diiodide: Applications to Synthesis of Asymmetric CABC Multi‐Block Copolymers and Their Unique Assembly Structures
inferredcites →https://doi.org/10.1002/chem.201600071openalex-snapshot
Azlactone Reaction Developments
inferredcites →https://doi.org/10.1002/marc.201200367openalex-snapshot
Amine‐Reactive Polymers Synthesized by RAFT Polymerization Using an Azlactone Functional Trithiocarbonate RAFT Agent
inferredcites →https://doi.org/10.1002/pi.5677openalex-snapshot
Poly(ethylene oxide)‐based block copolymer electrolytes for lithium metal batteries
inferredcites →https://doi.org/10.1002/pola.10007openalex-snapshot
Chemistry and technology of 2‐alkenyl azlactones
inferredcites →https://doi.org/10.1002/pola.22706openalex-snapshot
Polymerization of oligo(ethylene glycol) (meth)acrylates: Toward new generations of smart biocompatible materials
inferredcites →https://doi.org/10.1016/s0021-9673(01)89501-7openalex-snapshot
Immobilization of Protein A at high density on azlactone-functional polymeric beads and their use in affinity chromatography
inferredcites →https://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
inferredcites →https://doi.org/10.1021/acs.macromol.5b00178openalex-snapshot
One-Step Synthesis of Azlactone-Functionalized SG1-Based Alkoxyamine for Nitroxide-Mediated Polymerization and Bioconjugation
inferredcites →https://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
inferredcites →https://doi.org/10.1021/acsmacrolett.8b00026openalex-snapshot
Biocompatible Choline Iodide Catalysts for Green Living Radical Polymerization of Functional Polymers
inferredcites →https://doi.org/10.1021/ja4036016openalex-snapshot
Reversible Generation of a Carbon-Centered Radical from Alkyl Iodide Using Organic Salts and Their Application as Organic Catalysts in Living Radical Polymerization
inferredcites →https://doi.org/10.1021/la8024952openalex-snapshot
Surface-Anchored Poly(2-vinyl-4,4-dimethyl azlactone) Brushes as Templates for Enzyme Immobilization
inferredcites →https://doi.org/10.1021/ma2014589openalex-snapshot
Reversible Complexation Mediated Living Radical Polymerization (RCMP) Using Organic Catalysts
inferredcites →https://doi.org/10.1021/ma3001719openalex-snapshot
Atom Transfer Radical Polymerization (ATRP): Current Status and Future Perspectives
inferredcites →https://doi.org/10.1021/ma302244jopenalex-snapshot
Visible-Light-Induced Reversible Complexation Mediated Living Radical Polymerization of Methacrylates with Organic Catalysts
inferredcites →https://doi.org/10.1021/ma501569jopenalex-snapshot
Systematic Study on Alkyl Iodide Initiators in Living Radical Polymerization with Organic Catalysts
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/10.1039/c2py20714aopenalex-snapshot
Thermoresponsive block copolymers containing reactive azlactone groups and their bioconjugation with lysozyme
inferredcites →https://doi.org/10.1039/c6ra20164dopenalex-snapshot
PMDETA as an efficient catalyst for bulk reversible complexation mediated polymerization (RCMP) in the absence of additional metal salts and deoxygenation
inferredcites →https://doi.org/10.1039/c7cs00587copenalex-snapshot
Up in the air: oxygen tolerance in controlled/living radical polymerisation
inferredcites →https://doi.org/10.1039/c8ob01807copenalex-snapshot
Azlactone-based heterobifunctional linkers with orthogonal clickable groups: efficient tools for bioconjugation with complete atom economy
inferredcites →https://doi.org/10.1039/c9py00091gopenalex-snapshot
Iodine-mediated reversible-deactivation radical polymerization: a powerful strategy for polymer synthesis
inferredcites →https://doi.org/10.1039/d0py00493fopenalex-snapshot
Radical ring-opening polymerization of novel azlactone-functionalized vinyl cyclopropanes
inferredcites →https://doi.org/10.1039/d0py00939copenalex-snapshot
Recent development in halogen-bonding-catalyzed living radical polymerization
inferredcites →https://doi.org/10.1039/d2py00120aopenalex-snapshot
Reversible complexation mediated polymerization: an emerging type of organocatalytically controlled radical polymerization
inferredcites →https://doi.org/10.1071/ch12192openalex-snapshot
Introducing the Azlactone Functionality into Polymers through Controlled Radical Polymerization: Strategies and Recent Developments
inferredcites →https://doi.org/10.1351/pac-rep-08-04-03openalex-snapshot
Terminology for reversible-deactivation radical polymerization previously called "controlled" radical or "living" radical polymerization (IUPAC Recommendations 2010)

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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
inferred← citeshttps://doi.org/10.1002/pol.20251179openalex-snapshot
Nitroxide‐Mediated Polymerization Synthesis of Geminal Bisphosphonate‐Functionalized (Co)polymers and Their Affinity to Hydroxyapatite Surface
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/10.1039/d3py01322gopenalex-snapshot
One stone two birds: from one azlactone-functionalized monomer to a heterofunctional diblock copolymer
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