Works matching DE "RING formation (Chemistry)"
Results: 5000
The reversible modification of acrylate adhesive system by introducing anthracene groups.
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- Journal of Adhesion, 2024, v. 100, n. 3, p. 200, doi. 10.1080/00218464.2023.2211930
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Facile Synthesis of Spirocyclic Oxindole Scaffolds via Intermolecular [4 + 1] Cycloaddition of ortho-Quinone Methides with 3-Chlorooxindoles.
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- Organic Preparations & Procedures International, 2024, v. 56, n. 4, p. 350, doi. 10.1080/00304948.2024.2367850
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[1,2]‐Phospha‐Brook Rearrangement‐Initiated Palladium‐Catalyzed Cyclization Reaction of Isocyanides and o‐Bromobenzaldehydes: Access to 2H‐Isoindole‐1‐carboxamides and 2H‐Isoindole‐1‐carbonitriles
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- Chinese Journal of Chemistry, 2025, v. 43, n. 6, p. 620, doi. 10.1002/cjoc.202401015
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DABCO‐Mediated Photoelectrochemical Three‐Component Sulfonocyclization of 3‐Aza‐1,5‐dienes.
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- Chinese Journal of Chemistry, 2025, v. 43, n. 5, p. 491, doi. 10.1002/cjoc.202401048
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Radical Functionalization of 1,6‐Diene via Transannular Cyano Migration: Synthesis of Polysubstituted Cyclopentanes<sup>†</sup>.
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- Chinese Journal of Chemistry, 2025, v. 43, n. 4, p. 437, doi. 10.1002/cjoc.202401072
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Yb(OTf)<sub>3</sub>‐Catalyzed Asymmetric [3+3] Cycloaddition of N‐Vinyl Nitrones with Activated Cyclopropanes to Prepare 1,2‐Oxazines.
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- Chinese Journal of Chemistry, 2025, v. 43, n. 4, p. 417, doi. 10.1002/cjoc.202400937
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Copper‐Catalyzed Ring‐Opening Hydrosilylation and Hydroboration of Arylidenecyclopropanes.
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- Chinese Journal of Chemistry, 2025, v. 43, n. 4, p. 385, doi. 10.1002/cjoc.202400811
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Influence of Pore Size on Cycloaddition Reaction of CO<sub>2</sub> and Epoxide Catalyzed by Supported Imidazolium Ionic Liquids.
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- Chemical Engineering & Technology, 2025, v. 48, n. 1, p. 1, doi. 10.1002/ceat.202400134
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Divergent Total Syntheses of Six Crinipellin‐Type Diterpenoids through Tandem 4π‐Electrocyclization/Dicycloexpansion.
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- Angewandte Chemie, 2025, v. 137, n. 12, p. 1, doi. 10.1002/ange.202501008
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Halogenated Donor–Acceptor Cyclopropanes as Donor–Acceptor Cyclopropene Surrogates.
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- Angewandte Chemie, 2025, v. 137, n. 12, p. 1, doi. 10.1002/ange.202424823
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Genetic Incorporation of a Thioxanthone‐Containing Amino Acid for the Design of Artificial Photoenzymes.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202419022
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ALKYLTHIOBENZOTHIAZOLES DECORATED WITH 1,2,3-TRIAZOLE.
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- Journal of Chemistry & Technologies, 2024, v. 32, n. 4, p. 903, doi. 10.15421/jchemtech.v32i4.316457
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REGIOSELECTIVITY OF HALO- AND CHALCOGEN-INDUCED CYCLIZATION OF DIALLYLQUINAZOLIN-4-ONE.
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- Journal of Chemistry & Technologies, 2024, v. 32, n. 4, p. 837, doi. 10.15421/jchemtech.v32i4.316035
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Unveiling the synergistic interplay between Cu and Ni with ZIF-8 nanomaterials: a catalyst for the synthesis of triazole derivatives in nanoscale chemistry.
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- Research on Chemical Intermediates, 2025, v. 51, n. 3, p. 1389, doi. 10.1007/s11164-025-05520-9
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Simultaneous Cycloadditions in the Solid State via Supramolecular Assembly.
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- Angewandte Chemie, 2025, v. 137, n. 3, p. 1, doi. 10.1002/ange.202415567
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Access to Alkenyl Cyclobutanols by Ni‐Catalyzed Regio‐ and Enantio‐Selective syn‐Hydrometalative 4‐exo‐trig Cyclization of Alkynones.
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- Angewandte Chemie, 2025, v. 137, n. 3, p. 1, doi. 10.1002/ange.202415164
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Synthesis, Anti-inflammatory and in silico Studies of few novel 1,2,4-Triazole Derived Schiff Base Compounds.
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- Indian Journal of Pharmaceutical Education & Research, 2024, v. 58, n. 4, p. 1235, doi. 10.5530/ijper.58.4.136
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Stepwise, biradical nature of the [3+2] cycloaddition reaction between 4-nitrobenzonitrile N-oxide and simple ethene: a reexamination.
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 11/12, p. 670, doi. 10.1007/s10593-025-03391-x
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Mussel-Inspired Hydrogels Incorporating Graphite Derivatives for Soft Tissue Regeneration.
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- Nanomaterials (2079-4991), 2025, v. 15, n. 4, p. 276, doi. 10.3390/nano15040276
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Synthesis of Novel s -Indacene-1,5-dione and Isoxazole Derivatives via NaNO 2 -Catalyzed/Involved Transformation of Cyclopentenone-MBH Acetates.
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- Catalysts (2073-4344), 2025, v. 15, n. 2, p. 186, doi. 10.3390/catal15020186
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Synthesis of 2,2,5-Trisubstituted Tetrahydrofurans by Ferrocenium-Catalyzed Dehydrative Diol Cyclization Reactions.
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- Inorganics, 2025, v. 13, n. 2, p. 59, doi. 10.3390/inorganics13020059
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An Appealing, Robust Access to Furo-Fused Heteropolycycles.
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- Molecules, 2025, v. 30, n. 4, p. 948, doi. 10.3390/molecules30040948
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Iodine(III)-Containing Reagents in Photo-Assisted and Photo-Catalyzed Organic Synthesis.
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- Molecules, 2025, v. 30, n. 4, p. 784, doi. 10.3390/molecules30040784
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Pyrrolizine- and Indolizine-Derived Spirooxindoles: Synthesis, Antibacterial Activity and Inverse Docking Analysis.
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- Chemistry (2624-8549), 2025, v. 7, n. 1, p. 18, doi. 10.3390/chemistry7010018
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SINTHESIS AND STUDY OF THE ANTI-INFLAMMATORY ACTIVITY OF THE HYDRICHLORIDES OF α-[4'-CHLORO(FLUORO)PHENYL]-β-MORPHOLINO-4-SUBSTITUTED PROPIOPHENONES.
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- Electronic Journal of Natural Sciences, 2006, v. 6, n. 1, p. 30
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SYNTHESIS AND SOME CONVERSIONS OF 1-AMINO-3-METHYL-3-ETHYL-2-ETHOXYCARBONYL-3,4-DIHYDRONAPHTHALENE.
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- Electronic Journal of Natural Sciences, 2004, v. 3, n. 2, p. 6
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Cyclization of A11-.E- and 2Z-Geranylfarnesols by a Bacterial Triterpene Synthase: Insight into Sesterterpene Biosynthesis in Aleuritopteris Ferns.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 11, p. 2278, doi. 10.1271/bbb.130543
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Biomimetic Cyclization of Epoxide Precursors of Indole Mono-, Sesqui- and Diterpene Alkaloids by Lewis Acids.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 11, p. 2213, doi. 10.1271/bbb.110511
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Azido-Coronatine: A Useful Platform for "Click Chemistry"-Mediated Probe Synthesis for Bioorganic Studies.
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- Bioscience, Biotechnology & Biochemistry, 2010, v. 74, n. 10, p. 2092, doi. 10.1271/bbb.100518
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Biosynthesis of Resorcylic Acid Lactone (5S)-5-Hydroxylasiodiplodin in Lasiodiplodia theobromae.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 11, p. 2522, doi. 10.1271/bbb.90417
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Asymmetric Total Synthesis of ent-Sandaracopimaradiene, a Biosynthetic Intermediate of Oryzalexins.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 11, p. 2822, doi. 10.1271/bbb.70468
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Use of the Benzyl Mesylate for the Synthesis of Tetrahydrofuran Lignan: Syntheses of 7,8-trans, 7',8' -trans, 7,7'-cis, and 8,8'-cis -Virgatusin Stereoisomers.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 9, p. 2248, doi. 10.1271/bbb.70236
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Synthesis of Amino Tetrahydrofuran Lignan via an N,O-Heterocyclic Compound as an Intermediate.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 3, p. 741, doi. 10.1271/bbb.60575
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Synthesis of Quinolactacide via an Acyl Migration Reaction and Dehydrogenation with Manganese Dioxide, and Its Insecticidal Activities.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 1, p. 303, doi. 10.1271/bbb.70.303
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Efficient Route to (S)-Azetidine-2-carboxylic Acid.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 10, p. 1892, doi. 10.1271/bbb.69.1892
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Synthesis of (+)-Aptosimon, a 4-Oxofurofuran Lignan, by eryhto Selective Aldol Condensation and Stereoconvergent Cyclization as the Key Reactions.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 4, p. 838, doi. 10.1271/bbb.67.838
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Front Cover: Macromol. Chem. Phys. 24/2024.
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- Macromolecular Chemistry & Physics, 2024, v. 225, n. 24, p. 1, doi. 10.1002/macp.202470048
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- Article
Hydrophobic Bombyx mori Silk Fibroin: Routes to Functionalization with Alkyl Chains.
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- Macromolecular Chemistry & Physics, 2023, v. 224, n. 21, p. 1, doi. 10.1002/macp.202300145
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Synthesis and Reactions of Homoditopic Stable Nitrile N‐Oxide as a Powerful Tool for Catalyst‐Free Constructions of Macromolecular Architectures.
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- Macromolecular Chemistry & Physics, 2022, v. 223, n. 20, p. 1, doi. 10.1002/macp.202200183
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Sustainable Light‐Stimulated Synthesis of Cross‐Linked Polymer Microparticles.
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- Macromolecular Chemistry & Physics, 2022, v. 223, n. 13, p. 1, doi. 10.1002/macp.202100493
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SnOct<sub>2</sub>‐Catalyzed and Alcohol‐Initiated ROPS of l‐Lactide—Control of the Molecular Weight and the Role of Cyclization.
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- Macromolecular Chemistry & Physics, 2022, v. 223, n. 6, p. 1, doi. 10.1002/macp.202100464
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Phenolic Hydroxyl‐Functionalized Covalent–Organic Frameworks for Formal [3+2] Reaction.
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- Macromolecular Chemistry & Physics, 2022, v. 223, n. 6, p. 1, doi. 10.1002/macp.202100462
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Polymeric Blatter's Radical via CuAAC and ROMP.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 19, p. 1, doi. 10.1002/macp.202100194
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Highly Crosslinked and Clickable Poly(divinylbenzene) Microspheres by Type II Photoinitiated Precipitation Polymerization.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 9, p. 1, doi. 10.1002/macp.202100022
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Phototriggered Crosslinking and Surface Modification via Catalyst‐Free Functionalization of a New Orthogonal Agent Containing Nitrile N‐Oxide and o‐Nitrobenzyl Ether Moieties.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 6, p. 1, doi. 10.1002/macp.202000459
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An Efficiently Reworkable Thermosetting Adhesive Based on Photoreversible [4+4] Cycloaddition Reaction of Epoxy‐Based Prepolymer with Four Anthracene End Groups.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 2, p. 1, doi. 10.1002/macp.202170003
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An Efficiently Reworkable Thermosetting Adhesive Based on Photoreversible [4+4] Cycloaddition Reaction of Epoxy‐Based Prepolymer with Four Anthracene End Groups.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 2, p. 1, doi. 10.1002/macp.202000298
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Synthesis and Characterization of Polyrotaxanes Comprising γ‐CDs and Distal Azide‐Terminated PHEMA Using Propargylamine Monosubstituted β‐CDs as End Stoppers.
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- Macromolecular Chemistry & Physics, 2020, v. 221, n. 18, p. 1, doi. 10.1002/macp.202000157
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UV‐Light Responsive and Self‐Healable Ethylene/Propylene Copolymer Rubbers Based on Reversible [4 + 4] Cycloaddition of Anthracene Derivatives.
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- Macromolecular Chemistry & Physics, 2020, v. 221, n. 12, p. 1, doi. 10.1002/macp.202000096
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Synthesize Hyperbranched Polymers Carrying Two Reactive Handles via CuAAC Reaction and Thiol–Ene Chemistry.
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- Macromolecular Chemistry & Physics, 2019, v. 220, n. 17, p. N.PAG, doi. 10.1002/macp.201900221
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