Works matching Alkynes
Results: 5000
Frontispiz: Palladium‐Catalyzed Tail‐to‐Tail Reductive Dimerization of Terminal Alkynes to 2,3‐Dibranched Butadienes.
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- Angewandte Chemie, 2022, v. 134, n. 13, p. 1, doi. 10.1002/ange.202281361
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- Article
Palladium‐Catalyzed Tail‐to‐Tail Reductive Dimerization of Terminal Alkynes to 2,3‐Dibranched Butadienes.
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- Angewandte Chemie, 2022, v. 134, n. 13, p. 1, doi. 10.1002/ange.202116870
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POSS-based hybrid thermosets via photoinduced copper-catalyzed azide–alkyne cycloaddition click chemistry.
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- Designed Monomers & Polymers, 2016, v. 19, n. 2, p. 155, doi. 10.1080/15685551.2015.1124323
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A Facile Stereoselective Bis‐Trifluoromethylselenolation Reaction of Alkynes with AgSeCF<sub>3</sub> and N‐Bromosuccinimide.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 8, p. 1, doi. 10.1002/ajoc.202200319
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Alkyne Surrogates in Cycloaddition Reactions for the Preparation of Molecules of Interest.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 9, p. 2287, doi. 10.1002/ajoc.202100345
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Organocatalytic Oxidative Functionalizations of Alkynes.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 1, p. 63, doi. 10.1002/ajoc.201800632
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Palladium‐Catalyzed Denitrogenative Coupling of Aryldiazonium Salts with Terminal Alkynes for the Assembly of Internal Alkynes.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 40, p. 1, doi. 10.1002/ejoc.202400635
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A Salen-Co<sup>3+</sup> Catalyst for the Hydration of Terminal Alkynes and in Tandem Catalysis with Ru-TsDPEN for the One-Pot Transformation of Alkynes into Chiral Alcohols.
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- ChemCatChem, 2014, v. 6, n. 6, p. 1612, doi. 10.1002/cctc.201400071
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"Golden Age" of Homogeneous Catalytic Chemistry of Alkynes: Some Oxidative Transformations of Alkynes (A Review).
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- Kinetics & Catalysis, 2023, v. 64, n. 5, p. 521, doi. 10.1134/S0023158423050117
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"Golden Age" of Homogeneous Catalysis Chemistry of Alkynes: Dimerization and Oligomerization of Alkynes.
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- Kinetics & Catalysis, 2019, v. 60, n. 6, p. 689, doi. 10.1134/S0023158419060120
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Liquid-Phase Hydrogenation of Internal and Terminal Alkynes on Pd–Ag/Al<sub>2</sub>O<sub>3</sub> Catalyst.
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- Kinetics & Catalysis, 2019, v. 60, n. 5, p. 642, doi. 10.1134/S0023158419050069
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Supported catalysts based on Pd-In nanoparticles for the liquid- phase hydrogenation of terminal and internal alkynes: 2. catalytic properties.
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- Kinetics & Catalysis, 2016, v. 57, n. 5, p. 625, doi. 10.1134/S0023158416050141
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Catalytic 1,3‐H Atom Shift of a Terminal Benzylic Alkyne by Iron and Alkali Metal Silylamides – Switching between Allene and Internal Alkyne.
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- European Journal of Inorganic Chemistry, 2022, v. 2022, n. 6, p. 1, doi. 10.1002/ejic.202100955
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Internal Alkyne Regio- and Chemoselectivity using a Zwitterionic N-Heterocyclic Carbene Gold Catalyst in a Silver-Free Alkyne Hydration Reaction.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 24, p. 4106, doi. 10.1002/adsc.201601013
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Minutes Synthesis of 1,4,5-Trisubstituted 5-Dialkylamino-1,2,3-triazoles by 1-Copper(I)-Alkyne Controlled Tandem Process.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 2/3, p. 401, doi. 10.1002/adsc.201400471
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Chemoselective Synthesis of Unsymmetrical Internal Alkynes or Vinyl Sulfones via Palladium-Catalyzed Cross-Coupling Reaction of Sodium Sulfinates with Alkynes.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 9, p. 2029, doi. 10.1002/adsc.201300945
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Practical Methods for the Synthesis of Trifluoromethylated Alkynes: Oxidative Trifluoromethylation of Copper Acetylides and Alkynes.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 9, p. 2051, doi. 10.1002/adsc.201400057
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Silver-Catalyzed Alkyne Activation: The Surprising Ligand Effect.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 4, p. 692, doi. 10.1002/adsc.201300785
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Structural Determinants of Alkyne Reactivity in Copper-Catalyzed Azide-Alkyne Cycloadditions.
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- Molecules, 2016, v. 21, n. 12, p. 1697, doi. 10.3390/molecules21121697
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Well‐Defined Alkyne Metathesis Catalysts: Developments and Recent Applications.
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- Chemistry - A European Journal, 2019, v. 25, n. 13, p. 3190, doi. 10.1002/chem.201804511
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Nickel-Catalyzed [2+2+2] Cycloaddition of Alkyne-Nitriles with Alkynes Assisted by Lewis Acids: Efficient Synthesis of Fused Pyridines.
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- Chemistry - A European Journal, 2016, v. 22, n. 47, p. 16765, doi. 10.1002/chem.201603829
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Back Cover: Organomagnesium-Catalyzed Isomerization of Terminal Alkynes to Allenes and Internal Alkynes (Chem. Eur. J. 22/2015).
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- Chemistry - A European Journal, 2015, v. 21, n. 22, p. 8300, doi. 10.1002/chem.201590096
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Organomagnesium-Catalyzed Isomerization of Terminal Alkynes to Allenes and Internal Alkynes.
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- Chemistry - A European Journal, 2015, v. 21, n. 22, p. 8112, doi. 10.1002/chem.201500179
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Alkylation of Terminal Alkynes with Transient σ-Alkylpalladium(II) Complexes: A Carboalkynylation Route to Alkyl-Substituted Alkynes.
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- Chemistry - A European Journal, 2014, v. 20, n. 7, p. 1843, doi. 10.1002/chem.201303879
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Photoinitiated by Red Light (λ 625 nm) Iodosulfonylation of Internal Alkynes to Synthesize β-Iodovinyl Sulfones.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 12, p. 2102, doi. 10.1134/S1070428023120060
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Polar Solvent–Mediated Synthesis of Terminal Alkyne Derivatives of Thiazoles and Evaluation of Their Antidiabetic Activity.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 5, p. 801, doi. 10.1134/S1070428021050067
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Visible-Light-Induced Copper(I)-Catalyzed Azide-Alkyne Cycloaddition Initiated by Zinc Oxide Semiconductor Nanoparticles.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 5, p. 442, doi. 10.1002/ajoc.201500077
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Mild Oxidative Bromination of Alkenes and Alkynes with Zinc Bromide and Lead Tetraacetate.
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- Synthetic Communications, 2004, v. 34, n. 19, p. 3545, doi. 10.1081/SCC-200031007
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Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 42, p. 12431, doi. 10.1002/anie.201506075
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Recent Advances in Alkyne-Based Multicomponent Polymerizations.
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- Macromolecular Chemistry & Physics, 2016, v. 217, n. 2, p. 213, doi. 10.1002/macp.201500291
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Regioselective Metal-Free Click Polymerization of Azides and Alkynes.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 8, p. 818, doi. 10.1002/macp.201400571
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Metal-Free Cycloaddition of Internal Alkynes and Multifunctional Azides Under Solvent-Free Conditions.
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- Macromolecular Chemistry & Physics, 2014, v. 215, n. 17, p. 1603, doi. 10.1002/macp.201400149
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Controlling Chemoselectivity in Ruthenium(II)‐Induced Cyclization of Aniline‐Functionalized Alkynes.
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- Chemistry - A European Journal, 2024, v. 30, n. 69, p. 1, doi. 10.1002/chem.202402959
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Dirhodium(II)/XantPhos Catalyzed Synthesis of β‐(E)‐Vinylsilanes via Hydrosilylation and Isomerization from Alkynes.
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- Chemistry - A European Journal, 2024, v. 30, n. 64, p. 1, doi. 10.1002/chem.202402406
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Gold Trifluoromethyl Complexes as Efficient Regioselective Catalysts in Alkyne Hydration.
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- Chemistry - A European Journal, 2024, v. 30, n. 52, p. 1, doi. 10.1002/chem.202401753
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Visible‐Light‐Mediated [2+2] Photocycloadditions of Alkynes.
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202401501
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Recent Advancements in Metal‐Catalyst‐Free Multicomponent Radical Sulfonylation of Alkynes.
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202401386
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Metal‐Free Tunable 1,2‐Difunctionalization of Terminal Alkynes: Synthesis of β‐Substituted α,β‐Unsaturated Ketones.
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- Chemistry - A European Journal, 2023, v. 29, n. 67, p. 1, doi. 10.1002/chem.202302294
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Transition‐Metal‐Catalyzed Addition of Organosulfur Compounds to Alkynes and Alkenes: Catalysis and Catalyst Poisons.
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- Chemistry - A European Journal, 2023, v. 29, n. 64, p. 1, doi. 10.1002/chem.202302432
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Photoinduced NiH Catalysis with Trialkylamines for the Stereodivergent Transfer Semi‐Hydrogenation of Alkynes.
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- Chemistry - A European Journal, 2023, v. 29, n. 59, p. 1, doi. 10.1002/chem.202301636
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Hydrofluorination of Alkynes: From (E) to (Z).
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- Chemistry - A European Journal, 2023, v. 29, n. 58, p. 1, doi. 10.1002/chem.202301896
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Front Cover: Fe<sup>III</sup>‐Based Eutectic Mixtures as Multi‐task and Reusable Reaction Media for Efficient and Selective Conversion of Alkynes into Carbonyl Compounds (Chem. Eur. J. 57/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 57, p. 1, doi. 10.1002/chem.202301736
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Fe<sup>III</sup>‐Based Eutectic Mixtures as Multi‐task and Reusable Reaction Media for Efficient and Selective Conversion of Alkynes into Carbonyl Compounds.
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- Chemistry - A European Journal, 2023, v. 29, n. 57, p. 1, doi. 10.1002/chem.202301736
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Cover Feature: Cyanine‐ and Rhodamine‐Derived Alkynes for the Selective Targeting of Cancerous Mitochondria through Radical Thiol‐Yne Coupling in Live Cells (Chem. Eur. J. 45/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 45, p. 1, doi. 10.1002/chem.202302034
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Cyanine‐ and Rhodamine‐Derived Alkynes for the Selective Targeting of Cancerous Mitochondria through Radical Thiol‐Yne Coupling in Live Cells.
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- Chemistry - A European Journal, 2023, v. 29, n. 45, p. 1, doi. 10.1002/chem.202301340
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Highly Chemoselective Zn<sup>+2</sup>‐Catalyzed Hydrosilylation of Alkynes.
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- Chemistry - A European Journal, 2023, v. 29, n. 42, p. 1, doi. 10.1002/chem.202300798
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Frontispiece: Advances in Selective Electrocatalytic Hydrogenation of Alkynes to Alkenes.
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- Chemistry - A European Journal, 2023, v. 29, n. 15, p. 1, doi. 10.1002/chem.202381561
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Advances in Selective Electrocatalytic Hydrogenation of Alkynes to Alkenes.
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- Chemistry - A European Journal, 2023, v. 29, n. 15, p. 1, doi. 10.1002/chem.202202979
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Encapsulation of Palladium Carbide Subnanometric Species in Zeolite Boosts Highly Selective Semihydrogenation of Alkynes.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202313101
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Nickel‐Catalyzed Markovnikov‐Selective Hydrodifluoromethylation of Alkynes Using BrCF<sub>2</sub>H.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202305426
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