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.
The 66 checked references that resolve
resolves10.1039/c3gc41492bConversion of biomass platform molecules into fuel additives and liquid hydrocarbon fuels
resolves10.1039/b615413aProcess options for converting renewable feedstocks to bioproducts
resolves10.1039/C5EE02666KFurfural: a renewable and versatile platform molecule for the synthesis of chemicals and fuels
resolves10.1039/C8GC03541EBiobased phenol and furan derivative coupling for the synthesis of functional monomers
resolves10.1002/ejoc.200900749Synthesis 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-0259Photochemical [2+2] Cycloadditions. III. Addition of 4-Substituted 2-Cyclopentenones to Allene; Configuration Determination by Lanthanide-Induced Shift Studies.
resolves10.1021/ja027154uStereodivergent Synthesis of All 15-F<sub>2</sub> Isoprostanes
resolves10.1055/s-2007-983768Selective Synthesis of <b><i>ent</i></b>-15-<b><i>epi</i></b>-F<sub>2t</sub>-Isoprostane and a Deuterated Derivative
resolves10.1002/ejoc.201300382Photochemical and Thermal [2 + 2] Cycloaddition to Generate the Bicyclo[3.2.0]heptane Core of Bielschowskysin
resolves10.1021/jo051916xTotal 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/jo00001a070On 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-X4-hydroxycyclopent-2-en-1-one and derivatives as chiral synthetic equivalents of cyclopentadienone in asymmetric diels-alder reactions
resolves10.1021/ja00127a028Michael Additions of Functionalized Organozinc Reagents Mediated by Catalytic Quantities of Copper(I)
resolves10.1021/ja003119gNovel and Flexible Entries into Prostaglandins and Analogues Based on Ring Closing Alkyne Metathesis or Alkyne Cross Metathesis
resolves10.1021/ja0401702Total Synthesis of (−)-Incarvilline, (+)-Incarvine C, and (−)-Incarvillateine
resolves10.1039/B916506AThe thio-adduct facilitated, enzymatic kinetic resolution of 4-hydroxycyclopentenone and 4-hydroxycyclohexenone
resolves10.1039/b005520oA novel approach to bis-isoxazolines using a latent form of cyclopentadienone
resolves10.1016/S0040-4039(01)94824-5Terrein, an optically active prostaglandin synthon of fungal origin. II. Chemical conversion to 4()-acetoxy-2-cyclopentenone.
resolves10.1055/s-1978-24808Photochemische Bildung zweier [2+2]-Dimeren von Cyclopentadienon aus 5-Acetoxy-3-oxocyclopenten
resolves10.1080/10601320701681839Photodimerization of Coumarin Functionalized Poly(alkyl Acrylate) and Poly(alkyl Methacrylate) Random Copolymers: Influence of Copolymer Composition on Photocrosslinking
resolves10.1295/polymj.30.990Reversible Formation of Interpenetrating Polymer Network Structure in Organic-Inorganic Polymer Hybrids
resolves10.1016/j.polymer.2005.05.032Synthesis, characterization and photocross-linking of copolymers of furan and aliphatic hydroxyethylesters prepared by transesterification
resolves10.1021/ol403015sDynamic Covalent Bond Based on Reversible Photo [4 + 4] Cycloaddition of Anthracene for Construction of Double-Dynamic Polymers
resolves10.1021/ma012263zPEG-Based Hydrogel Synthesis via the Photodimerization of Anthracene Groups
resolves10.1016/j.polymer.2013.12.055Controlled synthesis of vinyl-functionalized homopolymers and block copolymers by RAFT polymerization of vinyl methacrylate
resolves10.1021/ma802057uWell-Defined Polymers Bearing Pendent Alkene Functionalities via Selective RAFT Polymerization
resolves10.1002/pola.21762Reversible addition–fragmentation chain transfer mediated radical polymerization of asymmetrical divinyl monomers targeting hyperbranched vinyl polymers
resolves10.1021/ma9804951Living Free-Radical Polymerization by Reversible Addition−Fragmentation Chain Transfer: The RAFT Process
resolves10.1039/C4GC02076FCatalytic routes towards acrylic acid, adipic acid and ε-caprolactam starting from biorenewables
resolves10.1039/C6PY00522EFunctionalisation of MWCNTs with poly(lauryl acrylate) polymerised by Cu(0)-mediated and RAFT methods
resolves10.1055/s-0030-1258534Microwave- or Microreactor-Assisted Conversion of Furfuryl Alcohols into 4-Hydroxy-2-cyclopentenones
resolves10.1002/jcc.21759Effect of the damping function in dispersion corrected density functional theory
resolves10.1002/jcc.23193Reply to ‘comment on “extending Hirshfeld‐I to bulk and periodic materials”’
resolves10.1063/1.454033A multicenter numerical integration scheme for polyatomic molecules
resolves10.1063/1.4975122NMR shieldings from density functional perturbation theory: GIPAW versus all-electron calculations
resolves10.1021/ma501267aImpact of Competitive Processes on Controlled Radical Polymerization
resolves10.1002/pol.1971.150090705Side‐chain crystallinity. I. Heats of fusion and melting transitions on selected homopolymers having long side chains
resolves10.1002/pol.1971.150091121Side‐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-xBiodegradable bio-based polyesters with controllable photo-crosslinkability, thermal and hydrolytic stability
resolves10.1139/v69-116Inefficiency 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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