Works matching DE "VINYLCYCLOPROPANES"
Results: 48
Bis(4-methoxybenzoyl)diethylgermane: A Highly Efficient Photoinitiator for the Polymerization of Vinylcyclopropanes.
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- Macromolecular Chemistry & Physics, 2016, v. 217, n. 24, p. 2686, doi. 10.1002/macp.201600463
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Organophotocatalyzed Alkyl/Arylsulfonylation of Vinylcyclopropanes.
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- Chemistry - A European Journal, 2024, v. 30, n. 5, p. 1, doi. 10.1002/chem.202303187
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Catalytic Isomerization of Substituted Vinylcyclopropanes.
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- Doklady Chemistry, 2019, v. 487, n. 1, p. 192, doi. 10.1134/S0012500819070115
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Synergistic Palladium-Phosphoric Acid Catalysis in (3 + 2) Cycloaddition Reactions between Vinylcyclopropanes and Imines.
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- Catalysts (2073-4344), 2020, v. 10, n. 2, p. 150, doi. 10.3390/catal10020150
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Synthesis Kinetics of Polymer/Copolymer Latexes via Radical Ring-Opening Emulsion Polymerization of Vinylcyclopropane.
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- Journal of Scientific Research, 2016, v. 8, n. 3, p. 463, doi. 10.3329/jsr.v8i3.28183
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An Enantioselective Cascade Cyclopropanation Reaction Catalyzed by Rhodium(I): Asymmetric Synthesis of Vinylcyclopropanes.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 22, p. 3512, doi. 10.1002/adsc.201600789
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Synthesis of Perfluoroalkyl-Substituted Vinylcyclopropanes by Way of Enhanced Neighboring Group Participation.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 19, p. 4071, doi. 10.1002/ejoc.201500565
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Development of low-shrinkage composites based on novel crosslinking vinylcyclopropanes.
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- Journal of Applied Polymer Science, 2017, v. 134, n. 48, p. n/a, doi. 10.1002/app.45577
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[(NHC)Ni<sup>II</sup>H]‐Catalyzed Cross‐Hydroalkenylation of Cyclopropenes with Alkynes: Cyclopentadiene Synthesis by [(NHC)Ni<sup>II</sup>]‐Assisted C−C Rearrangement.
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- Angewandte Chemie, 2019, v. 131, n. 17, p. 5758, doi. 10.1002/ange.201901255
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Pd‐Catalyzed Dearomatization of Anthranils with Vinylcyclopropanes by [4+3] Cyclization Reaction.
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- Angewandte Chemie, 2019, v. 131, n. 17, p. 5795, doi. 10.1002/ange.201901251
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Cobalt‐Catalyzed Reductive Dimethylcyclopropanation of 1,3‐Dienes.
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- Angewandte Chemie, 2018, v. 130, n. 42, p. 14098, doi. 10.1002/ange.201807542
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Cobalt‐Catalyzed Intramolecular Reactions between a Vinylcyclopropane and an Alkyne: Switchable [5+2] Cycloaddition and Homo‐Ene Pathways.
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- Angewandte Chemie, 2018, v. 130, n. 22, p. 6668, doi. 10.1002/ange.201803162
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Phosphine‐Catalyzed Activation of Vinylcyclopropanes: Rearrangement of Vinylcyclopropylketones to Cycloheptenones.
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- Angewandte Chemie, 2018, v. 130, n. 21, p. 6392, doi. 10.1002/ange.201800555
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Rhodium(I)-Catalyzed Bridged [5+2] Cycloaddition of cis-Allene-vinylcyclopropanes to Synthesize the Bicyclo[4.3.1]decane Skeleton.
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- Angewandte Chemie, 2017, v. 129, n. 30, p. 8793, doi. 10.1002/ange.201702288
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Zinc-Catalyzed Alkene Cyclopropanation through Zinc Vinyl Carbenoids Generated from Cyclopropenes.
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- Angewandte Chemie, 2015, v. 127, n. 41, p. 12307, doi. 10.1002/ange.201505954
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Photocatalytic Dearomative Intermolecular Seven‐Membered Ring Construction of Benzofurans.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 11, p. 1, doi. 10.1002/ajoc.202300467
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Rh<sup>I</sup>‐Catalyzed Intramolecular [3+2] Cycloaddition of 1‐Allene‐vinylcyclopropanes.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 8, p. 1609, doi. 10.1002/ajoc.201800294
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Metal‐Free Azidoarylation of Vinylcyclopropanes for the Synthesis of N<sub>3</sub>‐Containing Dihydronaphthalenes.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 2, p. 432, doi. 10.1002/ajoc.201700683
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Catalytic Cycloaddition Reactions of Ynol and Thioynol Ethers.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 24, p. 3469, doi. 10.1002/cjoc.202400607
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Rhodium(I)-Catalyzed C−C Bond Activation of Siloxyvinylcyclopropanes with Diazoesters.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 49, p. 15401, doi. 10.1002/anie.201609642
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Evaluation of Difunctional Vinylcyclopropanes as Reactive Diluents for the Development of Low-Shrinkage Composites.
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- Macromolecular Materials & Engineering, 2017, v. 302, n. 7, p. n/a, doi. 10.1002/mame.201700021
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Synthesis of acidic vinylcyclopropanes for dental applications.
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- Polymer International, 2017, v. 66, n. 10, p. 1410, doi. 10.1002/pi.5403
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Vinylcyclopropane [3+2] Cycloaddition with Acetylenic Sulfones Based on Visible Light Photocatalysis**.
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- Chemistry - A European Journal, 2022, v. 28, n. 18, p. 1, doi. 10.1002/chem.202104329
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Total synthesis of gelsemoxonine.
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- Pure & Applied Chemistry, 2012, v. 84, n. 7, p. 1643, doi. 10.1351/PAC-CON-11-10-25
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Divergent Rearrangements of Vinylcyclopropane into Skipped Diene and Cyclopentene: Mechanism, Scope, and Limitations.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 20, p. 2862, doi. 10.1002/ejoc.202100430
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The Retro‐Claisen Rearrangement of 2‐Vinylcyclopropylcarbonyl Substrates and the Question of its Synthetic Potential.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 24, p. 3517, doi. 10.1002/ejoc.202000136
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Ni(NHC) Catalyzed Rearrangement of 1‐Acyl‐2‐vinylcyclopropanes: Tackling a Mechanistic Puzzle by Combined Experimental and Computational Studies.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 36, p. 6285, doi. 10.1002/ejoc.201901096
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Synthesis of Vinylcyclopropane‐Fused Pyrazolone Derivatives by Sulfur Ylide‐Initiated 1,6‐Michael Addition‐Cyclization Reactions.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 34, p. 4723, doi. 10.1002/ejoc.201800710
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Ligand‐Controlled Regiodivergence in Nickel‐Catalyzed Vinylcyclopropane Rearrangement.
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- Angewandte Chemie, 2023, v. 135, n. 33, p. 1, doi. 10.1002/ange.202307826
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Photoredox Generation of Isothiouronyl Radical Cations: A New Platform in Covalent Radical Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 32, p. 1, doi. 10.1002/ange.202205596
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Cobalt‐Catalyzed Asymmetric Sequential Hydroboration/Isomerization/Hydroboration of 2‐Aryl Vinylcyclopropanes.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202205619
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Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β‐Unsaturated Esters.
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- Angewandte Chemie, 2022, v. 134, n. 25, p. 1, doi. 10.1002/ange.202202621
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Phosphine‐Catalyzed Enantioselective (3+2) Annulation of Vinylcyclopropanes with Imines for the Synthesis of Chiral Pyrrolidines.
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202203212
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Palladium‐Catalyzed Cascade to Benzoxepins by Using Vinyl‐Substituted Donor–Acceptor Cyclopropanes.
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- Angewandte Chemie, 2021, v. 133, n. 26, p. 14531, doi. 10.1002/ange.202102862
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Stereoselective Gold(I)‐Catalyzed Vinylcyclopropanation via Generation of a Sulfur‐Substituted Vinyl Carbene Equivalent.
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- Angewandte Chemie, 2021, v. 133, n. 8, p. 4116, doi. 10.1002/ange.202012664
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Utilizing Vinylcyclopropane Reactivity: Palladium‐Catalyzed Asymmetric [5+2] Dipolar Cycloadditions.
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- Angewandte Chemie, 2020, v. 132, n. 40, p. 17582, doi. 10.1002/ange.202006366
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Silylium‐Ion‐Promoted (5+1) Cycloaddition of Aryl‐Substituted Vinylcyclopropanes and Hydrosilanes Involving Aryl Migration.
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- Angewandte Chemie, 2020, v. 132, n. 29, p. 12284, doi. 10.1002/ange.202004320
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Photo-induced intramolecular dearomative [5 + 4] cycloaddition of arenes for the construction of highly strained medium-sized-rings.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46647-4
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Computational Insights into the Gold‐Catalyzed Ring‐Opening of Methylenecyclopropanes and Vinylcyclopropanes with Sulfonamides.
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- ChemCatChem, 2018, v. 10, n. 13, p. 2817, doi. 10.1002/cctc.201800237
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Palladium‐Catalyzed Amide Directed Regioselective γ‐Alkenylation of Unactivated Alkenes with Vinylcyclopropanes.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 42, p. 1, doi. 10.1002/ejoc.202400749
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Cover Feature: Catalytic Asymmetric Ring Opening Reactions of Vinylcyclopropanes (Eur. J. Org. Chem. 19/2024).
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- European Journal of Organic Chemistry, 2024, v. 27, n. 19, p. 1, doi. 10.1002/ejoc.202480504
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Catalytic Asymmetric Ring Opening Reactions of Vinylcyclopropanes.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 19, p. 1, doi. 10.1002/ejoc.202301225
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Formal Asymmetric (4+1) Annulation Reaction between Sulfur Ylides and 1,3-Dienes.
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- Chemistry - A European Journal, 2015, v. 21, n. 37, p. 12899, doi. 10.1002/chem.201502579
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Transition-Metal-Free Coupling Reaction of Vinylcyclopropanes with Aldehydes Catalyzed by Tin Hydride.
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- Chemistry - A European Journal, 2015, v. 21, n. 16, p. 6295, doi. 10.1002/chem.201406496
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Highly Enantioselective [3+2] Cycloaddition of Vinylcyclopropane with Nitroalkenes Catalyzed by Palladium(0) with a Chiral Bis( tert-amine) Ligand.
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- Chemistry - A European Journal, 2015, v. 21, n. 6, p. 2335, doi. 10.1002/chem.201405407
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Iridium Catalyzed Carbocyclizations: Efficient (5+2) Cycloadditions of Vinylcyclopropanes and Alkynes.
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- Chemistry - A European Journal, 2015, v. 21, n. 2, p. 531, doi. 10.1002/chem.201405729
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Evaluating the Thermal Vinylcyclopropane Rearrangement (VCPR) as a Practical Method for the Synthesis of Difluorinated Cyclopentenes: Experimental and Computational Studies of Rearrangement Stereospecificity.
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- Chemistry - A European Journal, 2014, v. 20, n. 44, p. 14305, doi. 10.1002/chem.201403737
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Divergent Fluorinations of Vinylcyclopropanes: Ring‐Opening 1,5‐Hydrofluorination and Ring‐Retaining 1,2‐Difluorination.
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- Chemistry - An Asian Journal, 2023, v. 18, n. 16, p. 1, doi. 10.1002/asia.202300476
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