On the public citation graph

Azlactone-based heterobifunctional linkers with orthogonal clickable groups: efficient tools for bioconjugation with complete atom economy

0 signed · 71 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/1521-3773(20010601)40:11<2004::aid-anie2004>3.0.co;2-5openalex-snapshot

Click Chemistry: Diverse Chemical Function from a Few Good Reactions

inferredcites →https://doi.org/10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4openalex-snapshot

A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

inferredcites →https://doi.org/10.1002/anie.201200002openalex-snapshot

Molecular Scaffolds Using Multiple Orthogonal Conjugations: Applications in Chemical Biology and Drug Discovery

inferredcites →https://doi.org/10.1002/anie.201209239openalex-snapshot

Organocatalytic, Regioselective Nucleophilic “Click” Addition of Thiols to Propiolic Acid Esters for Polymer–Polymer Coupling

inferredcites →https://doi.org/10.1002/anie.201307628openalex-snapshot

Antibody–Drug Conjugates: An Emerging Concept in Cancer Therapy

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/marc.201200367openalex-snapshot

Amine‐Reactive Polymers Synthesized by RAFT Polymerization Using an Azlactone Functional Trithiocarbonate RAFT Agent

inferredcites →https://doi.org/10.1002/pola.10007openalex-snapshot

Chemistry and technology of 2‐alkenyl azlactones

inferredcites →https://doi.org/10.1007/bf00845692openalex-snapshot

Role of the 6-amino groups of lysine in lysozyme

inferredcites →https://doi.org/10.1016/c2009-0-64240-9openalex-snapshot

Bioconjugate Techniques

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.ijpharm.2010.03.036openalex-snapshot

Biochemical and biophysical characterization of lysozyme modified by PEGylation

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.tetlet.2006.02.131openalex-snapshot

Dual side-reactions limit the utility of a key polymer therapeutic precursor

inferredcites →https://doi.org/10.1016/s0169-409x(03)00108-xopenalex-snapshot

Pharmacokinetic and biodistribution properties of poly(ethylene glycol)–protein conjugates

inferredcites →https://doi.org/10.1016/s0308-8146(96)00326-3openalex-snapshot

Cycloaddition reactions of conjugated dienoic carboxylic acids and esters with N-substituted maleimides and Schiff bases

inferredcites →https://doi.org/10.1021/acs.biochem.7b00536openalex-snapshot

Residue-Specific Peptide Modification: A Chemist’s Guide

inferredcites →https://doi.org/10.1021/acs.bioconjchem.8b00320openalex-snapshot

Tuning the Diels–Alder Reaction for Bioconjugation to Maleimide Drug-Linkers

inferredcites →https://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

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/bc0603790openalex-snapshot

Overcoming Limiting Side Reactions Associated with an NHS-Activated Precursor of Polymethacrylamide-Based Polymers

inferredcites →https://doi.org/10.1021/cr0783479openalex-snapshot

Cu-Catalyzed Azide−Alkyne Cycloaddition

inferredcites →https://doi.org/10.1021/cr200338qopenalex-snapshot

Strategies for Coupling Molecular Units if Subsequent Decoupling Is Required

inferredcites →https://doi.org/10.1021/jo00166a052openalex-snapshot

Consequences of intramolecular diyl trapping reactions using unactivated diylophiles. A short, convergent synthesis of hirsutene

inferredcites →https://doi.org/10.1021/jo00428a004openalex-snapshot

Facile synthesis of amino acid and peptide esters under mild conditions via cesium salts

inferredcites →https://doi.org/10.1021/ma100142wopenalex-snapshot

Synthesis, Characterization, and Bioactivity of Mid-Functional PolyHPMA−Lysozyme Bioconjugates

inferredcites →https://doi.org/10.1021/mz500654aopenalex-snapshot

Post-Fabrication Placement of Arbitrary Chemical Functionality on Microphase-Separated Thin Films of Amine-Reactive Block Copolymers

inferredcites →https://doi.org/10.1038/nmat4106openalex-snapshot

Smart hybrid materials by conjugation of responsive polymers to biomacromolecules

inferredcites →https://doi.org/10.1039/b407712aopenalex-snapshot

A new approach to bioconjugates for proteins and peptides (“pegylation”) utilising living radical polymerisation

inferredcites →https://doi.org/10.1039/b511113gopenalex-snapshot

The diverse chemistry of oxazol-5-(4H)-ones

inferredcites →https://doi.org/10.1039/b907061copenalex-snapshot

Synthesis and bioactivity of poly(HPMA)–lysozyme conjugates: the use of novel thiazolidine-2-thione coupling chemistry

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/10.1039/c2ob26409aopenalex-snapshot

Click reactions in protein chemistry: from the preparation of semisynthetic enzymes to new click enzymes

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/c2py20757eopenalex-snapshot

Poly(azlactone)s: versatile scaffolds for tandem post-polymerisation modification and glycopolymer synthesis

inferredcites →https://doi.org/10.1039/c3cc40588eopenalex-snapshot

Exploiting furan's versatile reactivity in reversible and irreversible orthogonal peptide labeling

inferredcites →https://doi.org/10.1039/c3ob41329bopenalex-snapshot

Bioorthogonal labelling of biomolecules: new functional handles and ligation methods

inferredcites →https://doi.org/10.1039/c4ob01632gopenalex-snapshot

Design strategies for bioorthogonal smart probes

inferredcites →https://doi.org/10.1039/c4py01108bopenalex-snapshot

RAFT-prepared α-difunctional poly(2-vinyl-4,4-dimethylazlactone)s and their derivatives: synthesis and effect of end-groups on aqueous inverse temperature solubility

inferredcites →https://doi.org/10.1039/c5cc00518copenalex-snapshot

Engineering of carbon based nanomaterials by ring-opening reactions of a reactive azlactone graphene platform

inferredcites →https://doi.org/10.1039/c5cs00048copenalex-snapshot

Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation

inferredcites →https://doi.org/10.1039/c5ob01457copenalex-snapshot

Copper-catalysed azide–alkyne cycloadditions (CuAAC): an update

inferredcites →https://doi.org/10.1039/c6ob00126bopenalex-snapshot

Selective chemical labeling of proteins

inferredcites →https://doi.org/10.1039/c6ob00808aopenalex-snapshot

Bioconjugation – using selective chemistry to enhance the properties of proteins and peptides as therapeutics and carriers

inferredcites →https://doi.org/10.1055/s-0036-1588647openalex-snapshot

5(4H)-Oxazolones as Effective Aminoacylation Reagents for the 3′-Terminus of RNA

inferredcites →https://doi.org/10.1071/ch12192openalex-snapshot

Introducing the Azlactone Functionality into Polymers through Controlled Radical Polymerization: Strategies and Recent Developments

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

inferred← citeshttps://doi.org/10.1002/ajoc.202000328openalex-snapshot

Proximity‐driven, Regioselective Chemical Modification of Peptides and Proteins

inferred← citeshttps://doi.org/10.1002/ejoc.201901350openalex-snapshot

Heteromultifunctional Oxazolones as Versatile Linkers for Click Chemistry Reactions

inferred← citeshttps://doi.org/10.1002/macp.201900500openalex-snapshot

In Situ Polymer Analogue Generation of Azlactone Functions at Poly(oxazoline)s for Peptide Conjugation

inferred← citeshttps://doi.org/10.1002/marc.202200420openalex-snapshot

Comparative Investigation of the Hydrolysis of Charge‐Shifting Polymers Derived from an Azlactone‐Based Polymer

inferred← citeshttps://doi.org/10.1002/slct.201803634openalex-snapshot

Regioselective Synthesis of Functionalized 1,3‐Thiazine‐4‐ones via Multicomponent Click Reaction Approach

inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2020.110081openalex-snapshot

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.polymer.2020.123062openalex-snapshot

Bioconjugates – From a specialized past to a diverse future

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/10.1016/j.trac.2019.03.028openalex-snapshot

Activity-based proteomic profiling: The application of photoaffinity probes in the target identification of bioactive molecules

inferred← citeshttps://doi.org/10.1021/acs.analchem.1c03695openalex-snapshot

A Quantification of Target Protein Biomarkers in Complex Media by Faradaic Shotgun Tagging

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/acscatal.5c02848openalex-snapshot

Dynamic Kinetic Resolution of Azlactones with Hydrazines via Negative Catalysis: Synthesis of α-Chiral Amino Acid Hydrazides and Their Preferential Enrichment Phenomenon

inferred← citeshttps://doi.org/10.1039/c8py01776jopenalex-snapshot

Structure-pDNA complexation and structure–cytotoxicity relationships of PEGylated, cationic aminoethyl-based polyacrylates with tunable topologies

inferred← citeshttps://doi.org/10.1039/c9tb01624dopenalex-snapshot

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/d0py00493fopenalex-snapshot

Radical ring-opening polymerization of novel azlactone-functionalized vinyl cyclopropanes

inferred← citeshttps://doi.org/10.1039/d0py00861copenalex-snapshot

Poly(2-isopropenyl-2-oxazoline) – a structural analogue to poly(vinyl azlactone) with Orthogonal Reactivity

inferred← citeshttps://doi.org/10.1039/d2bm01237eopenalex-snapshot

Chemical modification of proteins – challenges and trends at the start of the 2020s

inferred← citeshttps://doi.org/10.1039/d2py00660jopenalex-snapshot

Poly(2-isopropenyl-2-oxazoline) as a reactive polymer for materials development

inferred← citeshttps://doi.org/10.1039/d2py00873dopenalex-snapshot

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

inferred← citeshttps://doi.org/10.1039/d3py01322gopenalex-snapshot

One stone two birds: from one azlactone-functionalized monomer to a heterofunctional diblock copolymer

inferred← citeshttps://doi.org/10.70675/b6df86c2z6520z473ez9e10ze1740b9bc3aeopenalex-snapshot

Nouvelle génération d’AAV : un mélange de chimie organique et de vectorologie

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.