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UV-Curable Biobased Polyacrylates Based on a Multifunctional Monomer Derived from Furfural

https://doi.org/10.1021/acs.macromol.9b02659
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66/66 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

7 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 66 checked references that resolve
resolves10.1039/c3gc41492b
Conversion of biomass platform molecules into fuel additives and liquid hydrocarbon fuels
resolves10.1039/b615413a
Process options for converting renewable feedstocks to bioproducts
resolves10.1039/C5EE02666K
Furfural: a renewable and versatile platform molecule for the synthesis of chemicals and fuels
resolves10.1039/C8GC03541E
Biobased phenol and furan derivative coupling for the synthesis of functional monomers
resolves10.1016/S0040-4039(00)71357-8
A useful preparation of 4-substituted 5-hydroxy-3-oxocyclopentene
resolves10.1002/ejoc.200900749
Synthesis of Functionalized Bicyclo[3.2.0]heptanes – a Study of the [2+2] Photocycloaddition Reactions of 4‐Hydroxycyclopent‐2‐enone Derivatives
resolves10.3891/acta.chem.scand.42b-0259
Photochemical [2+2] Cycloadditions. III. Addition of 4-Substituted 2-Cyclopentenones to Allene; Configuration Determination by Lanthanide-Induced Shift Studies.
resolves10.1021/ja027154u
Stereodivergent Synthesis of All 15-F<sub>2</sub> Isoprostanes
resolves10.1055/s-2007-983768
Selective Synthesis of <b><i>ent</i></b>-15-<b><i>epi</i></b>-F<sub>2t</sub>-Isoprostane and a Deuterated Derivative
resolves10.1016/S0040-4020(01)81706-3
Studies directed towards the total synthesis of dicyclopenta[a,d]cyclooctane terpenoids
resolves10.1002/ejoc.201300382
Photochemical and Thermal [2 + 2] Cycloaddition to Generate the Bicyclo[3.2.0]­hept­ane Core of Bielschowskysin
resolves10.1016/j.tetlet.2012.01.010
Evaluation of a flow-photochemistry platform for the synthesis of compact modules
resolves10.1021/jo051916x
Total Synthesis of 8,12-<i>iso</i>-iPF<sub>3</sub><sub>α</sub>-VI, an EPA-Derived Isoprostane:  Stereoselective Introduction of the Fifth Asymmetric Center
resolves10.1021/jo00001a070
On the diastereofacial selectivity of Lewis acid-catalyzed carbon-carbon bond forming reactions of conjugated cyclic enones bearing electron-withdrawing substituents at the .gamma.-position
resolves10.1016/S0040-4020(01)85571-X
4-hydroxycyclopent-2-en-1-one and derivatives as chiral synthetic equivalents of cyclopentadienone in asymmetric diels-alder reactions
resolves10.1021/jo00269a006
An organozinc aid in alkylation and acylation of lithium enolates
resolves10.1016/S0040-4020(01)85596-4
Three-component coupling synthesis of prostaglandins. A simplified, general procedure
resolves10.1021/ja00127a028
Michael Additions of Functionalized Organozinc Reagents Mediated by Catalytic Quantities of Copper(I)
resolves10.1021/ja003119g
Novel and Flexible Entries into Prostaglandins and Analogues Based on Ring Closing Alkyne Metathesis or Alkyne Cross Metathesis
resolves10.1021/ja0401702
Total Synthesis of (−)-Incarvilline, (+)-Incarvine C, and (−)-Incarvillateine
resolves10.1039/B916506A
The thio-adduct facilitated, enzymatic kinetic resolution of 4-hydroxycyclopentenone and 4-hydroxycyclohexenone
resolves10.1039/b005520o
A novel approach to bis-isoxazolines using a latent form of cyclopentadienone
resolves10.1016/S0957-4166(01)00078-7
Synthesis of enantiopure bis-isoxazolines from (4R)-(+)-4-acetoxycyclopent-2-enone
resolves10.1016/S0040-4039(01)94824-5
Terrein, an optically active prostaglandin synthon of fungal origin. II. Chemical conversion to 4()-acetoxy-2-cyclopentenone.
resolves10.1055/s-1978-24808
Photochemische Bildung zweier [2+2]-Dimeren von Cyclopentadienon aus 5-Acetoxy-3-oxocyclopenten
resolves10.1080/10601320701681839
Photodimerization of Coumarin Functionalized Poly(alkyl Acrylate) and Poly(alkyl Methacrylate) Random Copolymers: Influence of Copolymer Composition on Photocrosslinking
resolves10.1295/polymj.30.990
Reversible Formation of Interpenetrating Polymer Network Structure in Organic-Inorganic Polymer Hybrids
resolves10.1080/00218460590922011
Development of a Light-Deactivatable PSA <i>Via</i> Photodimerization
resolves10.1002/app.1959.070020607
Photosensitive polymers. I. Cinnamate esters of poly(vinyl alcohol) and cellulose
resolves10.1002/app.1959.070020608
Photosensitive polymers. II. Sensitization of poly(vinyl cinnamate)
resolves10.1016/j.polymer.2005.05.032
Synthesis, characterization and photocross-linking of copolymers of furan and aliphatic hydroxyethylesters prepared by transesterification
resolves10.1021/ol403015s
Dynamic Covalent Bond Based on Reversible Photo [4 + 4] Cycloaddition of Anthracene for Construction of Double-Dynamic Polymers
resolves10.1016/j.eurpolymj.2013.10.024
Photo-induced crosslinking and thermal de-crosslinking in polynorbornenes bearing pendant anthracene groups
resolves10.1021/ma012263z
PEG-Based Hydrogel Synthesis via the Photodimerization of Anthracene Groups
resolves10.1002/macp.1996.021970502
Reversible photodimerisation of ω‐anthrylpolystyrenes
resolves10.1016/j.polymer.2013.12.055
Controlled synthesis of vinyl-functionalized homopolymers and block copolymers by RAFT polymerization of vinyl methacrylate
resolves10.1021/ma802057u
Well-Defined Polymers Bearing Pendent Alkene Functionalities via Selective RAFT Polymerization
resolves10.1002/pola.21762
Reversible addition–fragmentation chain transfer mediated radical polymerization of asymmetrical divinyl monomers targeting hyperbranched vinyl polymers
resolves10.1021/ma9804951
Living Free-Radical Polymerization by Reversible Addition−Fragmentation Chain Transfer:  The RAFT Process
resolves10.1039/C4GC02076F
Catalytic routes towards acrylic acid, adipic acid and ε-caprolactam starting from biorenewables
resolves10.1002/9781118229996
Industrial Organic Chemicals
resolves10.1039/C6PY00522E
Functionalisation of MWCNTs with poly(lauryl acrylate) polymerised by Cu(0)-mediated and RAFT methods
resolves10.1021/acs.analchem.5b00146
COCONUT—An Efficient Tool for Estimating Copolymer Compositions from Mass Spectra
resolves10.1055/s-0030-1258534
Microwave- or Microreactor-Assisted Conversion of Furfuryl Alcohols into 4-Hydroxy-2-cyclopentenones
resolves10.1016/S0957-4166(99)00445-0
Enzymatic kinetic resolution studies of racemic 4-hydroxycyclopent-2-en-1-one using Lipozyme IM®
resolves10.1103/PhysRevB.59.1758
From ultrasoft pseudopotentials to the projector augmented-wave method
resolves10.1103/PhysRevB.50.17953
Projector augmented-wave method
resolves10.1103/PhysRevLett.77.3865
Generalized Gradient Approximation Made Simple
resolves10.1002/jcc.21759
Effect of the damping function in dispersion corrected density functional theory
resolves10.1002/jcc.23088
Extending Hirshfeld‐I to bulk and periodic materials
resolves10.1002/jcc.23193
Reply to ‘comment on “extending Hirshfeld‐I to bulk and periodic materials”’
resolves10.1063/1.454033
A multicenter numerical integration scheme for polyatomic molecules
resolves10.1103/PhysRevB.63.245101
All-electron magnetic response with pseudopotentials: NMR chemical shifts
resolves10.1103/PhysRevB.76.024401
Calculation of NMR chemical shifts for extended systems using ultrasoft pseudopotentials
resolves10.1063/1.4975122
NMR shieldings from density functional perturbation theory: GIPAW versus all-electron calculations
resolves10.1016/j.progpolymsci.2017.11.002
Radical polymerization of acrylic monomers: An overview
resolves10.1021/ma501267a
Impact of Competitive Processes on Controlled Radical Polymerization
resolves10.1021/acs.macromol.6b01195
Intermolecular Transfer to Polymer in the Radical Polymerization of <i>n</i>-Butyl Acrylate
resolves10.1021/ma300410v
RAFT Agent Design and Synthesis
resolves10.1002/pol.1971.150090705
Side‐chain crystallinity. I. Heats of fusion and melting transitions on selected homopolymers having long side chains
resolves10.1002/pol.1971.150091121
Side‐chain crystallinity. II. Heats of fusion and melting transitions on selected copolymers incorporating <i>n</i>‐octadecyl acrylate or vinyl stearate
resolves10.1007/s10965-010-9526-x
Biodegradable bio-based polyesters with controllable photo-crosslinkability, thermal and hydrolytic stability
resolves10.1021/ja00871a039
<b>On the Mechanism of the Photodimerization of Cyclopentenone</b>
resolves10.1021/ja00975a069
On the Photodimerization of Cyclopentenone
resolves10.1021/ja00995a020
Photochemistry of cyclopentenone in various media
resolves10.1139/v69-116
Inefficiency and reversibility in the photodimerization of 2-cyclopentenone
The 7 references without a DOI — listed, not checked
no DOI — not checkedRadiation Curing
no DOI — not checkedDelzenne, G.; Laridon, U. Photosensitive Polymers-Synthesis and Properties of Coumarin-Modified Polymers; Industrie Chimique Belge-Belgische Chemische Industrie, 1966; p 158.
no DOI — not checkedVanpoucke, D. E. P. Fingerprinting defects in diamond: Partitioning the vibrational spectrum. 2020, arXiv preprint arXiv:2001.06277. https://arxiv.org/abs/2001.06277.
no DOI — not checkedHIVE-tools v4.x, 2005. https://github.com/DannyVanpoucke/HIVE4-tools.
no DOI — not checkedLebedev, V. I.; Laikov, D. A Quadrature Formula for the Sphere of the 131st Algebraic Order of Accuracy; Pleiades Publishing, Ltd.: Doklady Mathematics, 1999; pp 477–481.
no DOI — not checkedHandbook of Radical Polymerization
no DOI — not checkedExperimental chemical shifts are generally presented relative to a specific reference. We have chosen to present the calculated chemical shifts in their absolute calculated form, allowing for direct comparison to calculations using different methods. One might consider performing a shift on the calculated spectrum using a calculated reference or the experimental data directly. However, as we discuss in the SI, no unique shift value exists in the case of sub-ppm resolution spectra.
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