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Introducing the aza-Michael addition reaction between acrylate and dihydropyrimidin-2(1 H )-thione into polymer chemistry

https://doi.org/10.1039/d2py01130a
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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/adsc.201400904openalex-snapshot
Multicomponent Syntheses based upon Copper‐Catalyzed Alkyne‐Azide Cycloaddition
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Polypeptoids synthesis based on Ugi reaction: Advances and perspectives
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Antioxidant Polymers via the Kabachnik‐Fields Reaction to Control Cellular Oxidative Stress
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Multicomponent Reactions and Multicomponent Cascade Reactions for the Synthesis of Sequence‐Controlled Polymers
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The Hantzsch Reaction in Polymer Chemistry: From Synthetic Methods to Applications
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Stimuli‐Responsive Multifunctional Phenylboronic Acid Polymers Via Multicomponent Reactions: From Synthesis to Application
inferredcites →https://doi.org/10.1002/marc.202100642openalex-snapshot
Recent Advances in Diversity‐Oriented Polymerization Using Cu‐Catalyzed Multicomponent Reactions
inferredcites →https://doi.org/10.1007/s11426-016-0219-4openalex-snapshot
Training the old dog new tricks: the applications of the Biginelli reaction in polymer chemistry
inferredcites →https://doi.org/10.1007/s41061-017-0153-4openalex-snapshot
An Update on Isocyanide-Based Multicomponent Reactions in Polymer Science
inferredcites →https://doi.org/10.1016/j.bmcl.2006.06.006openalex-snapshot
A practical and green approach toward synthesis of N3-substituted dihydropyrimidinones: Using Aza-Michael addition reaction catalyzed by KF/Al2O3
inferredcites →https://doi.org/10.1016/j.ejmech.2017.10.073openalex-snapshot
Biological activity of dihydropyrimidinone (DHPM) derivatives: A systematic review
inferredcites →https://doi.org/10.1016/j.isci.2019.100754openalex-snapshot
High-Throughput Preparation of Antibacterial Polymers from Natural Product Derivatives via the Hantzsch Reaction
inferredcites →https://doi.org/10.1016/j.mtchem.2022.100948openalex-snapshot
Effective strategy for polymer synthesis: multicomponent reactions and click polymerization
inferredcites →https://doi.org/10.1016/j.tet.2007.05.108openalex-snapshot
Michael additions of dihydropyrimidines and 2-amino-1,3,4-thiadiazoles to α,β-ethylenic compounds: using polyethylene glycols as a green reaction media
inferredcites →https://doi.org/10.1016/s0040-4020(01)87971-0openalex-snapshot
100 years of the biginelli dihydropyrimidine synthesis
inferredcites →https://doi.org/10.1021/acs.biomac.8b00592openalex-snapshot
Biocompatible Unimolecular Micelles Obtained via the Passerini Reaction as Versatile Nanocarriers for Potential Medical Applications
inferredcites →https://doi.org/10.1021/acs.chemmater.1c03897openalex-snapshot
Antioxidant Polymers via the Ugi Reaction for In Vivo Protection of UV-Induced Oxidative Stress
inferredcites →https://doi.org/10.1021/acs.macromol.7b00465openalex-snapshot
50th Anniversary Perspective: Polymer Functionalization
inferredcites →https://doi.org/10.1021/acsabm.9b00799openalex-snapshot
Multicomponent Reactions-Based Modified/Functionalized Materials in the Biomedical Platforms
inferredcites →https://doi.org/10.1021/acscombsci.8b00072openalex-snapshot
Materials Functionalization with Multicomponent Reactions: State of the Art
inferredcites →https://doi.org/10.1021/acsmacrolett.1c00720openalex-snapshot
Magnetic Self-Healing Hydrogel from Difunctional Polymers Prepared via the Kabachnik–Fields Reaction
inferredcites →https://doi.org/10.1021/acsmacrolett.5b00428openalex-snapshot
Postpolymerization Modification of Poly(dihydropyrimidin-2(1H)-thione)s via the Thiourea–Haloalkane Reaction to Prepare Functional Polymers
inferredcites →https://doi.org/10.1021/acsmacrolett.5b00637openalex-snapshot
Multicomponent Copolycondensates via the Simultaneous Hantzsch and Biginelli Reactions
inferredcites →https://doi.org/10.1021/acsmacrolett.6b00530openalex-snapshot
Ugi Reaction of Natural Amino Acids: A General Route toward Facile Synthesis of Polypeptoids for Bioapplications
inferredcites →https://doi.org/10.1021/ja1113003openalex-snapshot
Introducing Multicomponent Reactions to Polymer Science: Passerini Reactions of Renewable Monomers
inferredcites →https://doi.org/10.1021/ja312592eopenalex-snapshot
Cu-Catalyzed Multicomponent Polymerization To Synthesize a Library of Poly(N-sulfonylamidines)
inferredcites →https://doi.org/10.1021/jacs.1c00243openalex-snapshot
Sulfur Conversion to Multifunctional Poly(O-thiocarbamate)s through Multicomponent Polymerizations of Sulfur, Diols, and Diisocyanides
inferredcites →https://doi.org/10.1021/jacs.1c08332openalex-snapshot
De Novo Design of Entropy-Driven Polymers Resistant to Bacterial Attachment via Multicomponent Reactions
inferredcites →https://doi.org/10.1021/jacs.6b04695openalex-snapshot
Diversity-Oriented Polymerization: One-Shot Synthesis of Library of Graft and Dendronized Polymers by Cu-Catalyzed Multicomponent Polymerization
inferredcites →https://doi.org/10.1021/jacs.6b05035openalex-snapshot
Metal-Free, Multicomponent Synthesis of Pyrrole-Based π-Conjugated Polymers from Imines, Acid Chlorides, and Alkynes
inferredcites →https://doi.org/10.1021/jacs.6b12767openalex-snapshot
Metal-Free Multicomponent Tandem Polymerizations of Alkynes, Amines, and Formaldehyde toward Structure- and Sequence-Controlled Luminescent Polyheterocycles
inferredcites →https://doi.org/10.1021/jacs.8b01576openalex-snapshot
High Throughput Preparation of UV-Protective Polymers from Essential Oil Extracts via the Biginelli Reaction
inferredcites →https://doi.org/10.1021/jacs.8b02886openalex-snapshot
Room Temperature One-Step Conversion from Elemental Sulfur to Functional Polythioureas through Catalyst-Free Multicomponent Polymerizations
inferredcites →https://doi.org/10.1021/ma500504wopenalex-snapshot
Diversely Substituted Polyamides: Macromolecular Design Using the Ugi Four-Component Reaction
inferredcites →https://doi.org/10.1021/mz300456popenalex-snapshot
Sequence Regulated Poly(ester-amide)s Based on Passerini Reaction
inferredcites →https://doi.org/10.1021/mz500139copenalex-snapshot
Efficient Multicomponent Postpolymerization Modification Based on Kabachnik-Fields Reaction
inferredcites →https://doi.org/10.1038/ncomms8411openalex-snapshot
A palladium-catalysed multicomponent coupling approach to conjugated poly(1,3-dipoles) and polyheterocycles
inferredcites →https://doi.org/10.1038/s41467-020-20027-0openalex-snapshot
High-throughput preparation of radioprotective polymers via Hantzsch’s reaction for in vivo X-ray damage determination
inferredcites →https://doi.org/10.1039/c3py00553dopenalex-snapshot
A new insight into the Biginelli reaction: the dawn of multicomponent click chemistry?
inferredcites →https://doi.org/10.1039/c3py01486jopenalex-snapshot
‘One pot’ synthesis of well-defined poly(aminophosphonate)s: time for the Kabachnik–Fields reaction on the stage of polymer chemistry
inferredcites →https://doi.org/10.1039/c5py01398dopenalex-snapshot
The Ugi reaction in polymer chemistry: syntheses, applications and perspectives
inferredcites →https://doi.org/10.1039/c7py01313bopenalex-snapshot
Polymer synthesis by mimicking nature's strategy: the combination of ultra-fast RAFT and the Biginelli reaction
inferredcites →https://doi.org/10.1039/d0py00503gopenalex-snapshot
Fluorescent polymers via post-polymerization modification of Biginelli-type polymers for cellular protection against UV damage
inferredcites →https://doi.org/10.1039/d1py00176kopenalex-snapshot
A multi-responsive self-healing hydrogel for controlled release of curcumin

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.4664247openalex-extracted
Fast-Curing Bio-Based Thermoset Foams Produced Via Michael Addition Using Fatty Acid-Based Acetoacetate and Acrylate
inferred← citeshttps://doi.org/10.1002/ejoc.202300451openalex-snapshot
Aza‐Michael Reaction: A Decade Later – Is the Research Over?
inferred← citeshttps://doi.org/10.1007/s10934-025-01789-8openalex-snapshot
Innovative application of high nitrogen magnetic MOF as a catalyst in the aza-Michael reaction
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2024.112968openalex-snapshot
Fast-curing bio-based thermoset foams produced via the Michael 1,4-addition using fatty acid-based acetoacetate and acrylate
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2025.114218openalex-snapshot
Synthesis and multi-tunable thermoresponsive behaviors of hyperbranched Y-junction-bearing copolymers
inferred← citeshttps://doi.org/10.1016/j.porgcoat.2026.110646openalex-snapshot
Zinc dimethacrylate-modified epoxy coating for corrosion protection and self-healing
inferred← citeshttps://doi.org/10.1021/acs.biomac.3c00992openalex-snapshot
Amphiphilic Block Copolymers PEG-b-PMTCs: Synthesis, Self-Assembly, Degradation Properties and Biocompatibility
inferred← citeshttps://doi.org/10.1021/acsabm.5c01081openalex-snapshot
Mannose-Decorated Stimuli-Responsive Fluorescent Poly(aminoamide) Microgels for Lectin Binding and Sensing
inferred← citeshttps://doi.org/10.1021/acsmacrolett.3c00572openalex-snapshot
Superhydrophobic Coatings Composed of Multifunctional Polymers Synthesized Using Successive Modification of Dihydropyrimidin-2(1H)-thione
inferred← citeshttps://doi.org/10.1021/acsmacrolett.4c00063openalex-snapshot
Ferrocene-Based Antioxidant Self-Healing Hydrogel via the Biginelli Reaction for Wound Healing
inferred← citeshttps://doi.org/10.1021/acsomega.5c07913openalex-snapshot
Coloration of Ethyleneamine-Diacrylate-Based Porous Polymer-Toluene Systems Induced by the Christiansen Effect: Color Control by the Molecular Design of the Polymer Networks
inferred← citeshttps://doi.org/10.1038/s41467-025-59027-3openalex-snapshot
Heterocycle-based dynamic covalent chemistry for dynamic functional materials
inferred← citeshttps://doi.org/10.1080/00397911.2025.2572083openalex-snapshot
Pseudo-seven-component double Ugi reaction with 2,2’-(hexane-1,6-diylbis(oxy))dibenzaldehyde for the synthesis of bis- carboxamides
inferred← citeshttps://doi.org/10.3390/molecules27227886openalex-snapshot
Stepping Further from Coupling Tools: Development of Functional Polymers via the Biginelli Reaction
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