Works about LEWIS acids
Results: 2669
Iron/Rhodium Bimetallic Lewis Acid/Transition Metal Relay Catalysis for Alkynylation/Cyclotrimerization Sequential Reactions Toward Isoindolinone Derivatives from N,O -Cyclic Acetals.
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- Catalysts (2073-4344), 2025, v. 15, n. 2, p. 151, doi. 10.3390/catal15020151
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Conjugated phthalocyanine-based framework as artificial SEI for over 400 Wh kg−1 lithium-metal battery.
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- National Science Review, 2025, v. 12, n. 2, p. 1, doi. 10.1093/nsr/nwae443
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Preparation of unsaturated MIL-101(Cr) with Lewis acid sites for the extraordinary adsorption of anionic dyes.
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- NPJ Clean Water, 2025, v. 8, n. 1, p. 1, doi. 10.1038/s41545-024-00413-7
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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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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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Polyether Synthesis through Reductive Etherification Reaction Strategy.
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- Macromolecular Chemistry & Physics, 2023, v. 224, n. 24, p. 1, doi. 10.1002/macp.202300063
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Room‐Temperature Lewis Acid Organocatalysts for Bulk Ring‐Opening Polymerization of Bis‐Lithium N‐Heterocyclic Carbenes Complexes Activated on ε‐Caprolactone: Synthetic, Experimental, and Density Functional Theory of Mechanistic Studies
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- Macromolecular Chemistry & Physics, 2023, v. 224, n. 17, p. 1, doi. 10.1002/macp.202300129
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Direct Observation of a Cyclic Vinyl Polymer Prepared by Anionic Polymerization using N‐Heterocyclic Carbene and Subsequent Ring‐Closure without Highly Diluted Conditions.
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- Macromolecular Chemistry & Physics, 2020, v. 221, n. 10, p. 1, doi. 10.1002/macp.202000004
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Preparation, Structure, Reactivity, Lewis Acidic and Fluorescence Properties of Arylpyridine Based Boron C,N‐Chelates Featuring Weakly Coordinating Anions.
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- Chemistry - A European Journal, 2024, v. 30, n. 71, p. 1, doi. 10.1002/chem.202403263
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Front Cover: Secondary Sphere Lewis Acid Activated Heme Superoxo Adducts Mimic Crucial Non‐Covalent Interactions in IDO/TDO Heme Dioxygenases (Chem. Eur. J. 68/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202486801
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Neutral Adducts of Molybdenum Hexafluoride: Structure and Bonding in MoF<sub>6</sub>(NC<sub>5</sub>H<sub>5</sub>) and MoF<sub>6</sub>(NC<sub>5</sub>H<sub>5</sub>)<sub>2</sub>.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402749
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Secondary Sphere Lewis Acid Activated Heme Superoxo Adducts Mimic Crucial Non‐Covalent Interactions in IDO/TDO Heme Dioxygenases.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402310
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Lewis Acid Regulation Strategy for Constructing D‐A‐A Covalent Organic Frameworks with Enhanced Photocatalytic Organic Conversion.
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- Chemistry - A European Journal, 2024, v. 30, n. 67, p. 1, doi. 10.1002/chem.202402736
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Chlorodefluorination Induced by Gallium‐Based Lewis Acids.
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- Chemistry - A European Journal, 2024, v. 30, n. 65, p. 1, doi. 10.1002/chem.202403226
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Gold Meets Selenium: Dual Activation of Selenium‐Containing Propargyl Alcohols Towards the Synthesis of 2H‐Chromenes and Mechanistic Insights.
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- Chemistry - A European Journal, 2024, v. 30, n. 62, p. 1, doi. 10.1002/chem.202402426
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Ficini Reaction with Acrylates for the Stereoselective Synthesis of Aminocyclobutanes.
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- Chemistry - A European Journal, 2024, v. 30, n. 58, p. 1, doi. 10.1002/chem.202401810
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Chemoselectivity Switch between Enantioselective [2,3]‐Wittig Rearrangement and Conia‐Ene‐Type Reactions of Propargyloxyoxindoles.
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- Chemistry - A European Journal, 2024, v. 30, n. 56, p. 1, doi. 10.1002/chem.202402556
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Well‐Defined Highly‐Coordinated Copper(III) Iodide and Pincer Tris(trifluoromethyl)copper Complexes.
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- Chemistry - A European Journal, 2024, v. 30, n. 54, p. 1, doi. 10.1002/chem.202401791
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Luminescent Platinum(II) Complexes with Stimuli‐Responsive Flexible Lewis Pair Ligands: Spectroscopic and Computational Studies.
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- Chemistry - A European Journal, 2024, v. 30, n. 53, p. 1, doi. 10.1002/chem.202401657
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Anions as Lewis Acids in Noncovalent Bonds.
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- Chemistry - A European Journal, 2024, v. 30, n. 51, p. 1, doi. 10.1002/chem.202402267
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Elucidating Mechanism and Selectivity in Pyridine Functionalization Through Silylium Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 51, p. 1, doi. 10.1002/chem.202402078
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Revisiting the Mechanism of Asymmetric Ni‐Catalyzed Reductive Carbo‐Carboxylation with CO<sub>2</sub>: The Additives Affect the Product Selectivity.
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- Chemistry - A European Journal, 2024, v. 30, n. 49, p. 1, doi. 10.1002/chem.202401631
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Cover Feature: Lewis Acid Catalyzed Cyclopropane Ring‐Opening‐Cyclization Cascade Using Thioureas as a N,N‐bisnucleophile: Synthesis of Bicyclic Furo‐, Pyrano‐, and Pyrrololactams via a Formal [4+1]‐Addition (Chem. Eur. J. 48/2024)
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- Chemistry - A European Journal, 2024, v. 30, n. 48, p. 1, doi. 10.1002/chem.202484804
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Multicomponent Synthesis of 3(2H)‐Furanones Initiated by Copper(II)‐Catalyzed Alkyne‐Carbonyl Cross Metathesis.
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- Chemistry - A European Journal, 2024, v. 30, n. 48, p. 1, doi. 10.1002/chem.202401999
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Lewis Acid Catalyzed Cyclopropane Ring‐Opening‐Cyclization Cascade Using Thioureas as a N,N‐bisnucleophile: Synthesis of Bicyclic Furo‐, Pyrano‐, and Pyrrololactams via a Formal [4+1]‐Addition.
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- Chemistry - A European Journal, 2024, v. 30, n. 48, p. 1, doi. 10.1002/chem.202401332
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Direct Access to Benzolactams and Benzolactones via Nickel Catalyzed Carbonylation with CO<sub>2</sub>.
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- Chemistry - A European Journal, 2024, v. 30, n. 47, p. 1, doi. 10.1002/chem.202401658
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Hydrosilylation of Arynes with Silanes and Silicon‐Based Polymer.
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- Chemistry - A European Journal, 2024, v. 30, n. 47, p. 1, doi. 10.1002/chem.202401440
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Structural Flexibility is a Decisive Factor in FLP Dihydrogen Cleavage with Tetrahedral Lewis Acids: A Silane Case Study.
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- Chemistry - A European Journal, 2024, v. 30, n. 46, p. 1, doi. 10.1002/chem.202401912
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A Phosphanyl Phosphagermene and its Reactivity.
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- Chemistry - A European Journal, 2024, v. 30, n. 46, p. 1, doi. 10.1002/chem.202401736
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Hydrosilylation of Olefins Activated on Highly Lewis‐Acidic Calcium Cation.
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- Chemistry - A European Journal, 2024, v. 30, n. 45, p. 1, doi. 10.1002/chem.202401322
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Cover Feature: Synthesis and Lewis Acid Properties of Neutral Silver(III) Adducts Containing the Ag<sup>III</sup>(CF<sub>3</sub>)<sub>3</sub> Moiety (Chem. Eur. J. 43/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202400881
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Synthesis and Lewis Acid Properties of Neutral Silver(III) Adducts Containing the Ag<sup>III</sup>(CF<sub>3</sub>)<sub>3</sub> Moiety.
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202400881
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Reactivity of a Neutral Yttrium(III) Trimethyl Complex toward Brønsted and Lewis Acids.
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- Chemistry - A European Journal, 2024, v. 30, n. 41, p. 1, doi. 10.1002/chem.202401687
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Tridentate Lewis Acids Based on Tribenzotriquinacene Chalices.
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- Chemistry - A European Journal, 2024, v. 30, n. 39, p. 1, doi. 10.1002/chem.202401072
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High‐Entropy Lanthanide–Organic Framework as an Efficient Heterogeneous Catalyst for Cycloaddition of CO<sub>2</sub> with Epoxides and Knoevenagel Condensation.
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- Chemistry - A European Journal, 2024, v. 30, n. 39, p. 1, doi. 10.1002/chem.202400756
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Organocatalyzed Asymmetric Conjugate Addition of Alcohols to β‐Fluoroalkyl Vinylsulfones by Bifunctional Phosphonium Salt Catalyst.
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- Chemistry - A European Journal, 2024, v. 30, n. 38, p. 1, doi. 10.1002/chem.202401325
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A Highly Sterically Encumbered Boron Lewis Acid Enabled by an Organotellurium‐Based Ligand.
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- Chemistry - A European Journal, 2024, v. 30, n. 36, p. 1, doi. 10.1002/chem.202401231
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Suppressing Cis/Trans 'Ring‐Flipping' in Organoaluminium(III)‐2‐Pyridyl Dimers–Design Strategies Towards Lewis Acid Catalysts for Alkene Oligomerisation.
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- Chemistry - A European Journal, 2024, v. 30, n. 28, p. 1, doi. 10.1002/chem.202303872
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Selectivity in Adduct Formation of a Bidentate Boron Lewis Acid.
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- Chemistry - A European Journal, 2024, v. 30, n. 27, p. 1, doi. 10.1002/chem.202400081
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C−F Bond Insertion: An Emerging Strategy for Constructing Fluorinated Molecules.
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- Chemistry - A European Journal, 2024, v. 30, n. 20, p. 1, doi. 10.1002/chem.202304229
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Controlling the Activation at Ni<sup>II</sup>−CO<sub>2</sub><sup>2−</sup> Moieties through Lewis Acid Interactions in the Second Coordination Sphere.
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- Chemistry - A European Journal, 2024, v. 30, n. 18, p. 1, doi. 10.1002/chem.202303112
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Stabilization of sp‐Hybridized Nitrogen Cation by Lewis Acid‐Base Complex Formation with Intramolecular Iodine.
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- Chemistry - A European Journal, 2024, v. 30, n. 5, p. 1, doi. 10.1002/chem.202303393
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Quo Vadis CO<sub>2</sub> Activation: Catalytic Reduction of CO<sub>2</sub> to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles.
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- Chemistry - A European Journal, 2024, v. 30, n. 5, p. 1, doi. 10.1002/chem.202303380
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Ring‐Opening of 1,3‐Imidazole Based Mesoionic Carbenes (iMICs) and Ring‐Closing Clicks: Facile Access to iMIC‐Compounds.
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- Chemistry - A European Journal, 2024, v. 30, n. 3, p. 1, doi. 10.1002/chem.202303652
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The Field of Main Group Lewis Acids and Lewis Superacids: Important Basics and Recent Developments.
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- Chemistry - A European Journal, 2024, v. 30, n. 1, p. 1, doi. 10.1002/chem.202302457
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Carbon Dioxide Hydrogenation to Formate Catalyzed by a Neutral, Coordinatively Saturated Tris‐Carbonyl Mn(I)‐PNP Pincer‐Type Complex.
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- Chemistry - A European Journal, 2023, v. 29, n. 70, p. 1, doi. 10.1002/chem.202302642
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P<sup>I</sup> and P<sup>III</sup> Ions Supported by BZIMPY Ligands.
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- Chemistry - A European Journal, 2023, v. 29, n. 70, p. 1, doi. 10.1002/chem.202302558
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Chalcogen Bonding Catalysis: Tellurium, the Last Frontier?
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- Chemistry - A European Journal, 2023, v. 29, n. 69, p. 1, doi. 10.1002/chem.202302755
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Beryllium‐Mediated Halide and Aryl Transfer onto Silicon.
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- Chemistry - A European Journal, 2023, v. 29, n. 66, p. 1, doi. 10.1002/chem.202302652
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Metal‐Free Catalytic Hydrogenolysis of Chlorosilanes into Hydrosilanes with "Inverse" Frustrated Lewis Pairs.
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- Chemistry - A European Journal, 2023, v. 29, n. 61, p. 1, doi. 10.1002/chem.202302155
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