Works matching DE "VINYL ethers"
Results: 398
Accuracy of Selective Laser Melted Bar Retaining Mandibular Implant-Assisted Overdenture: An In Vitro Comparison of Different Impression Materials and Techniques.
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- Journal of Oral Implantology, 2023, v. 49, n. 6, p. 590, doi. 10.1563/aaid-joi-D-23-00068
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Ring-Expansion Living Cationic Polymerization of Vinyl Ethers: Optimized Ring Propagation.
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- Macromolecular Symposia, 2015, v. 350, n. 1, p. 105, doi. 10.1002/masy.201400044
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Thermal and real-time FTIR spectroscopic analysis of the photopolymerization of diepoxide-vinyl ether mixtures.
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- Journal of Thermal Analysis & Calorimetry, 2004, v. 78, n. 1, p. 153, doi. 10.1023/B:JTAN.0000042163.86565.cf
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A theoretical investigation of the regio- and stereoselectivities of the [3 + 2] cycloaddition reaction between ethyl vinyl ether and substituted α-alkoxynitrones.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2022, v. 141, n. 5, p. 1, doi. 10.1007/s00214-022-02874-w
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A DFT study on the molecular mechanism of the conjugated nitroalkenes polymerization process initiated by selected unsaturated nucleophiles.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2020, v. 139, n. 7, p. 1, doi. 10.1007/s00214-020-02627-7
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Theoretical investigation on the decomposition reaction mechanisms and kinetics of methyl vinyl ether initialized by OH radical.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2017, v. 136, n. 1, p. 1, doi. 10.1007/s00214-016-2044-0
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A spin-coupled study of the Claisen rearrangement of allyl vinyl ether.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2006, v. 115, n. 4, p. 212, doi. 10.1007/s00214-005-0007-y
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1,2-Bis(trifluoromethyl)ethene-1,2-dicarbonitrile and Vinyl Ethers: Cyclic Ketene Imines on the Pathway to 1 : 2 Cycloadducts.
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- Helvetica Chimica Acta, 2012, v. 95, n. 5, p. 673, doi. 10.1002/hlca.201200047
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1,2-Bis(trifluoromethyl)ethene-1,2-dicarbonitrile: (2+2) Cycloadditions with Vinyl Ethers.
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- Helvetica Chimica Acta, 2012, v. 95, n. 1, p. 1, doi. 10.1002/hlca.201100449
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Cycloadditions of Bifunctional Vinyl Ethers with Electrophilic Alkenes through Tetramethylene Zwitterion Intermediates.
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- Helvetica Chimica Acta, 2005, v. 88, n. 6, p. 1397
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A new route for the synthesis of 1,4,2-dioxazoles from hydroxamic acids.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 11/12, p. 805, doi. 10.1007/s10593-024-03275-6
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A Structural Modification of Berberine Using CH Acids and Ethoxyethylenes Based on Them.
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- Chemistry of Heterocyclic Compounds, 2022, v. 58, n. 11, p. 621, doi. 10.1007/s10593-022-03135-1
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Addition reaction of various azoles to perfluoromethyl vinyl ether.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 6, p. 666, doi. 10.1007/s10593-021-02965-9
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6-Hydroxyaurone aminomethyl derivatives in the inverse electron-demand Diels–Alder reaction.
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- Chemistry of Heterocyclic Compounds, 2019, v. 55, n. 12, p. 1179, doi. 10.1007/s10593-019-02598-z
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Reduction and Cycloaddition of Heteroalkenes at Ga(I) Bisamide Center.
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- Reactions (2624-781X), 2024, v. 5, n. 1, p. 213, doi. 10.3390/reactions5010009
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Cross-Linked Solid Polymer-Based Catholyte for Solid-State Lithium-Sulfur Batteries.
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- Batteries, 2023, v. 9, n. 7, p. 341, doi. 10.3390/batteries9070341
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Characterization of cenosphere-reinforced vinyl ester composites.
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- Journal of Elastomers & Plastics, 2018, v. 50, n. 2, p. 95, doi. 10.1177/0095244317708591
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Vinylation of Betulin with Calcium Carbide.
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- Doklady Chemistry, 2022, v. 506, n. 2, p. 211, doi. 10.1134/S0012500822700124
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Cationic Copolymerization of Cholesterol Vinyl Ether with Methyl Vinyl Sulfide: Towards New Biologically Active Oligomers.
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- Doklady Chemistry, 2019, v. 489, n. 2, p. 288, doi. 10.1134/S0012500819120036
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Cationic Copolymerization of Cholesterol Vinyl Ether with N-Allenylpyrrolidone: A Route to Pharmacologically Promising Oligomers.
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- Doklady Chemistry, 2019, v. 485, n. 2, p. 112, doi. 10.1134/S0012500819040037
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Homo- and copolymers of vinyl glycerol ethers.
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- Doklady Chemistry, 2013, v. 449, n. 1, p. 81, doi. 10.1134/S0012500813030038
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Synthesis, biological and computational evaluation of novel cyanomethyl vinyl ether derivatives.
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- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1344042
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Quantification of the degradation products of sevoflurane using four brands of CO[sub 2] absorbent in a standard anesthetic circuit.
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- Journal of Anesthesia, 2000, v. 14, n. 3, p. 143, doi. 10.1007/s005400070022
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An alternating copolymer of maleic anhydride and ethyl vinyl ether: synthesis in supercritical carbon dioxide, characterization, and properties.
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- Designed Monomers & Polymers, 2013, v. 16, n. 3, p. 283, doi. 10.1080/15685551.2012.747144
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Co-polymerization of Isobutyl/4-Hydroxybutyl Vinyl Ether and Maleic Anhydride.
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- Designed Monomers & Polymers, 2010, v. 13, n. 1, p. 1, doi. 10.1163/138577209X12591392377612
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Controlled cationic polymerization of methyl vinyl ether with a semi-continuous process.
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- Designed Monomers & Polymers, 2001, v. 4, n. 2, p. 195, doi. 10.1163/156855500300203403
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Atmospheric Chemistry of 2-Methoxypropene and 2-Ethoxypropene: Kinetics and Mechanism Study of Reactions with Ozone.
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- Atmosphere, 2018, v. 9, n. 10, p. 401, doi. 10.3390/atmos9100401
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Comparative Evaluation of Surface Detail Reproduction and Dimensional Stability of Poly Ether, Vinyl Siloxane, and Vinyl Siloxane Ether Impression Materials: An In vitro Study.
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- Journal of Pharmacy & Bioallied Sciences, 2021, v. 13, p. S851, doi. 10.4103/jpbs.JPBS_819_20
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Comparative evaluation of surface detail reproduction and dimensional stability of poly ether, vinyl siloxane, and vinyl siloxane ether impression materials: An In vitro study.
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- Journal of Pharmacy & Bioallied Sciences, 2021, v. 13, p. 851, doi. 10.4103/jpbs.JPBS_819_20
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SYNTHESIS AND CHARACTERIZATION OF P(St-B-MMA), P(St-B-BA) AND POLY(MA-co-IBVE) BY USING...
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- Chinese Journal of Polymer Science (World Scientific Publishing Company), 2000, v. 18, n. 4, p. 384
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Novel alkyd-type coating resins produced using cationic polymerization.
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- Journal of Coatings Technology & Research, 2015, v. 12, n. 4, p. 633, doi. 10.1007/s11998-015-9667-2
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An efficient stereoselective synthesis of functionalized vinyl ethers.
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- Journal of the Iranian Chemical Society, 2014, v. 11, n. 5, p. 1483, doi. 10.1007/s13738-014-0418-6
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Synthesis of Fluorinated Amides Starting from Carbohydrates Based on the Claisen Rearrangement.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 2, p. 1, doi. 10.1002/ejoc.202101378
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Synthesis of (±)‐epi‐Jungianol by the Gold(I)‐Catalyzed Propargyl Claisen Rearrangement/Hydroarylation Cascade Reaction of Propargyl Vinyl Ethers.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 8, p. 1266, doi. 10.1002/ejoc.202001555
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Primary Vinyl Ethers as Acetylene Surrogate: A Flexible Tool for Deuterium‐Labeled Pyrazole Synthesis.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 29, p. 4571, doi. 10.1002/ejoc.202000674
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Direct Stereoselective β‐Arylation of Enol Ethers by a Decarboxylative Heck‐Type Reaction.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 14, p. 2052, doi. 10.1002/ejoc.201901877
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(Het)aryl Difluoromethyl‐Substituted β‐Alkoxyenones: Synthesis and Heterocyclizations.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 9, p. 1069, doi. 10.1002/ejoc.201901833
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2,3,3,3‐Tetrafluoropropene (HFO‐1234yf) as a CF<sub>3</sub>‐Building Block: Synthesis of Enol Ethers and Vinyl Sulfides.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 47, p. 7666, doi. 10.1002/ejoc.201901445
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Intermolecular Aminoallylation of Alkenes Using Allyl‐Oxyphthalimide Derivatives: A Case Study in Radical Polarity Effects.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 40, p. 6796, doi. 10.1002/ejoc.201901071
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A Domino Strategy for the Synthesis of 2H‐Pyrans from Propargyl Vinyl Ethers.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 8, p. 1784, doi. 10.1002/ejoc.201801847
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Aromatic Claisen Rearrangements of Benzyl Ketene Acetals: Conversion of Benzylic Alcohols to (ortho-Tolyl)acetates.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 2, p. 252, doi. 10.1002/ejoc.201601354
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Conjugation of Bioactive Molecules to a Fluorescent Dithiomaleimide by Photoinduced and BEt<sub>3</sub>-Initiated Thio-Click Reactions.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 35, p. 7675, doi. 10.1002/ejoc.201501116
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Copolymers of Diallyldimethylammonium Chloride and Vinyl Ether of Monoethanolamine: Synthesis, Flocculating, and Antimicrobial Properties.
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- Journal of Surfactants & Detergents, 2019, v. 22, n. 5, p. 1129, doi. 10.1002/jsde.12283
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Living Cationic Polymerization of Vinyl Ethers through a Photoinduced Radical Oxidation/Addition/Deactivation Sequence.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 2, p. 519, doi. 10.1002/anie.201609357
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Vinyl Ether/Tetrazine Pair for the Traceless Release of Alcohols in Cells.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 1, p. 243, doi. 10.1002/anie.201609607
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Alternating Sequence Control for Carboxylic Acid and Hydroxy Pendant Groups by Controlled Radical Cyclopolymerization of a Divinyl Monomer Carrying a Cleavable Spacer.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 47, p. 14584, doi. 10.1002/anie.201607169
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Sodium Salts of Anionic Chiral Cobalt(III) Complexes as Catalysts of the Enantioselective Povarov Reaction.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 38, p. 11209, doi. 10.1002/anie.201504790
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Unique Curing Properties through Living Polymerization in Crosslinking Materials: Polyurethane Photopolymers from Vinyl Ether Building Blocks.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 19, p. 5789, doi. 10.1002/anie.201412218
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Cationic RAFT Polymerization Using ppm Concentrations of Organic Acid.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 6, p. 1924, doi. 10.1002/anie.201410858
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Synthesis and characterization of poly(vinyl alcohol-co-aspartic acid) copolymers.
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- Polimery, 2010, v. 55, n. 7/8, p. 562, doi. 10.14314/polimery.2010.562
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