Works matching Lewis, C. S., 1898-1963
Results: 5000
Lewis Base Catalyzed C−S Bond Formation Through Methyl C(sp<sup>3</sup>)‐H Thiocyanation of Indoles.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 3, p. 1, doi. 10.1002/ajoc.202300495
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Lewis Acid Coordination Redirects S‐Nitrosothiol Signaling Output.
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- Angewandte Chemie, 2020, v. 132, n. 27, p. 10946, doi. 10.1002/ange.202001450
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Contrasting Frustrated Lewis Pair Reactivity with Selenium- and Boron-Based Lewis Acids.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 37, p. 11292, doi. 10.1002/anie.201605239
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Catalytic Degradation of Aliphatic Ethers using the Lewis Superacidic Bis(perfluoropinacolato)silane.
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- ChemCatChem, 2023, v. 15, n. 11, p. 1, doi. 10.1002/cctc.202300281
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Catalytic Hydrodefluorination of C−F Bonds by an Air‐Stable P<sup>III</sup> Lewis Acid.
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- Chemistry - A European Journal, 2018, v. 24, n. 25, p. 6543, doi. 10.1002/chem.201801305
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Effect of Ligands on the Lewis Acidity of the Metal and the Binding of N‐Bases to Iridium Pincer Complexes.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 10, p. 1389, doi. 10.1002/ejic.201801341
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Lewis Acidic Boranes, Lewis Bases, and Equilibrium Constants: A Reliable Scaffold for a Quantitative Lewis Acidity/Basicity Scale.
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- Chemistry - A European Journal, 2021, v. 27, n. 12, p. 4070, doi. 10.1002/chem.202003916
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Tandem Catalytic Depolymerization of Lignin by Water-Tolerant Lewis Acids and Rhodium Complexes.
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- ChemSusChem, 2016, v. 9, n. 16, p. 2074, doi. 10.1002/cssc.201600683
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Versatile Catalytic Hydrogenation Using A Simple Tin(IV) Lewis Acid.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 14958, doi. 10.1002/ange.201606639
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The Performance‐Determining Role of Lewis Bases in Dye‐Sensitized Solar Cells Employing Copper‐Bisphenanthroline Redox Mediators.
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- Advanced Energy Materials, 2020, v. 10, n. 37, p. 1, doi. 10.1002/aenm.202002067
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Versatile Catalytic Hydrogenation Using A Simple Tin(IV) Lewis Acid.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 47, p. 14738, doi. 10.1002/anie.201606639
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Lewis Acid Catalysis of Nb<sub>2</sub>O<sub>5</sub> for Reactions of Carboxylic Acid Derivatives in the Presence of Basic Inhibitors.
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- ChemCatChem, 2019, v. 11, n. 1, p. 383, doi. 10.1002/cctc.201801239
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Establishing the Coordination Chemistry of Antimony(V) Cations: Systematic Assessment of Ph<sub>4</sub>Sb(OTf) and Ph<sub>3</sub>Sb(OTf)<sub>2</sub> as Lewis Acceptors.
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- Chemistry - A European Journal, 2015, v. 21, n. 21, p. 7902, doi. 10.1002/chem.201406469
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Quantum chemical investigation of donor–acceptor complexes of trimethylaluminum with Lewis bases of group 15 elements.
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- International Journal of Quantum Chemistry, 2007, v. 107, n. 13, p. 2372, doi. 10.1002/qua.21329
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SOBRE LOS MITOS DEL REY ARTURO Y DE LA MAGIA: GUERRA EN EL CIELO DE CHARLES WILLIAMS Y ESA HORRIBLE FORTALEZA DE C. S. LEWIS.
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- Miscelanea Comillas, 2021, v. 79, n. 155, p. 499, doi. 10.14422/mis.v79.i155.y2021.003
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Structure-Activity Correlations for Brønsted Acid, Lewis Acid, and Photocatalyzed Reactions of Exfoliated Crystalline Niobium Oxides.
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- ChemCatChem, 2017, v. 9, n. 1, p. 144, doi. 10.1002/cctc.201601131
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Lewis and Clarks’ Tempest: The ‘perfect storm’ of November 1805, Oregon, USA.
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- Holocene, 2011, v. 21, n. 4, p. 693, doi. 10.1177/0959683610391319
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Acid-Base Pairs in Lewis Acidic Zeolites Promote Direct Aldol Reactions by Soft Enolization.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 34, p. 9835, doi. 10.1002/anie.201502939
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A Dimeric Gallium Hydrazide as an Active Lewis Pair - Complexation and Activation of Me<sub>2</sub>GaH and Various Heterocumulenes.
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- Zeitschrift für Anorganische und Allgemeine Chemie, 2017, v. 643, n. 5, p. 387, doi. 10.1002/zaac.201600456
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The role of the Lewis acid−base properties in the supramolecular association of 1,2,5-chalcogenadiazoles.
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- Canadian Journal of Chemistry, 2013, v. 91, n. 5, p. 338, doi. 10.1139/cjc-2012-0323
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Shedding Light on the Lewis Acid Catalysis in Organic Transformations Using a Zn-MOF Microflower and Its ZnO Nanorod.
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- Catalysis Letters, 2023, v. 153, n. 3, p. 887, doi. 10.1007/s10562-022-04004-4
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Metal‐Free Catalytic Formation of a Donor‐Acceptor‐Donor Molecule and Its Lewis Acid‐Adduct Singlet Diradical with High‐Efficient NIR‐II Photothermal Conversion.
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- Angewandte Chemie, 2024, v. 136, n. 19, p. 1, doi. 10.1002/ange.202400913
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Lewis Acid Behavior of SF<sub>4</sub>: Synthesis, Characterization, and Computational Study of Adducts of SF<sub>4</sub> with Pyridine and Pyridine Derivatives.
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- Chemistry - A European Journal, 2015, v. 21, n. 16, p. 6247, doi. 10.1002/chem.201406359
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Palabra creadora y visión poética del mundo. Los comienzos de la fantasía épica en C. S. Lewis.
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- OCNOS: Journal of Reading Research / Revista de Estudios sobre Lectura, 2011, n. 7, p. 29, doi. 10.18239/ocnos_2011.07.03
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C. S. LEWIS: ZNANSTVENA DJELA O SREDNJOVJEKOVLJU I KNJIŽEVNA KRITIKA.
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- Church in the World / Crkva u Svijetu, 2023, v. 58, n. 2, p. 265, doi. 10.34075/cs.58.2.6
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Systematic Assessment of the Catalytic Reactivity of Frustrated Lewis Pairs in C-H Bond Activation.
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- Molecules, 2024, v. 29, n. 1, p. 24, doi. 10.3390/molecules29010024
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Lewis Acid-Base Interaction-Controlled ortho-Selective C−H Borylation of Aryl Sulfides.
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- Angewandte Chemie, 2017, v. 129, n. 6, p. 1517, doi. 10.1002/ange.201610041
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Non-Covalent Interactions of the Lewis Acids Cu–X, Ag–X, and Au–X (X = F and Cl) with Nine Simple Lewis Bases B: A Systematic Investigation of Coinage–Metal Bonds by Ab Initio Calculations.
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- Inorganics, 2021, v. 9, n. 2, p. 13, doi. 10.3390/inorganics9020013
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ERA C. S. LEWIS UM INCLUSIVISTA?
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- Perspectiva Teológica, 2024, v. 56, n. 3, p. 593, doi. 10.20911/21768757v56n3p593/2024
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A Study of [3+2] Cycloaddition Reaction of Hydrazonoyl Chloride and β‐Oxodithioester Under Lewis Acid Catalysis: Stereoselective Synthesis of (Z)‐1,3,4‐Thiadiazol‐2(3H)‐Ylidenes.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 6, p. 1432, doi. 10.1002/ajoc.202100197
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Revealing Defect Passivation and Charge Extraction by Ultrafast Spectroscopy in Perovskite Solar Cells through a Multifunctional Lewis Base Additive Approach.
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- Solar RRL, 2024, v. 8, n. 21, p. 1, doi. 10.1002/solr.202400589
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Highly Efficient One-Pot Synthesis of COS-Based Block Copolymers by Using Organic Lewis Pairs.
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- Molecules, 2018, v. 23, n. 2, p. 298, doi. 10.3390/molecules23020298
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Lewis Acid Guests in a {P<sub>8</sub>W<sub>48</sub>} Archetypal Polyoxotungstate Host: Enhanced Proton Conductivity via Metal‐Oxo Cluster within Cluster Assemblies.
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13230, doi. 10.1002/ange.201806086
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Site‐Selective Pyridine C−H Alkylation with Alcohols and Thiols via Single‐Electron Transfer of Frustrated Lewis Pairs.
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- Angewandte Chemie, 2022, v. 134, n. 51, p. 1, doi. 10.1002/ange.202213857
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Elucidating the Reactivity of Vicinal Dicarbenoids: From Lewis Adduct Formation to B-C Bond Activation.
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- Chemistry - A European Journal, 2016, v. 22, n. 39, p. 13815, doi. 10.1002/chem.201603234
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Triarylborane‐Functionalized Au<sub>8</sub>Ag<sub>8</sub>(CCR)<sub>16</sub> Nanocluster with Enhanced Lewis Acidity.
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- Advanced Materials Interfaces, 2023, v. 10, n. 1, p. 1, doi. 10.1002/admi.202201657
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Understanding the C−F Bond Activation Mediated by Frustrated Lewis Pairs: Crucial Role of Non‐covalent Interactions.
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- Chemistry - A European Journal, 2021, v. 27, n. 11, p. 3823, doi. 10.1002/chem.202004733
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Reactivity-Tuning in Frustrated Lewis Pairs: Nucleophilicity and Lewis Basicity of Sterically Hindered Phosphines.
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- Chemistry - A European Journal, 2017, v. 23, n. 31, p. 7422, doi. 10.1002/chem.201701080
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Effects of Lewis Basicity and Acidity on σ-Hole Interactions in Carbon-Bearing Complexes: A Comparative Ab Initio Study.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 21, p. 13023, doi. 10.3390/ijms232113023
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Lewis Acid‐Catalyzed Diastereoselective C−C Bond Insertion of Diazo Esters into Secondary Benzylic Halides for the Synthesis of α,β‐Diaryl‐β‐haloesters.
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- Angewandte Chemie, 2022, v. 134, n. 29, p. 1, doi. 10.1002/ange.202204462
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Reactions of Al‐N Based Active Lewis Pairs with Ketones and 1,2‐Diketones: Insertion into Al‐N Bonds, C‐C and C‐N Bond Formation and a Tricyclic Saturated Tetraaza Compound.
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- European Journal of Inorganic Chemistry, 2020, v. 2020, n. 39, p. 3760, doi. 10.1002/ejic.202000570
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Cooperative Activation of Isocyanates by Al-N-Based Active Lewis Pairs and the Generation of a C<sub>5</sub> Chain by Simultaneous Formation of Two C-C Bonds.
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- Chemistry - A European Journal, 2017, v. 23, n. 25, p. 6129, doi. 10.1002/chem.201604630
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Reversible C−H Activation, Facile C−B/B−H Metathesis and Apparent Hydroboration Catalysis by a Dimethylxanthene‐Based Frustrated Lewis Pair.
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- Chemistry - A European Journal, 2018, v. 24, n. 41, p. 10531, doi. 10.1002/chem.201801871
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Taming the Lewis Superacidity of Non‐Planar Boranes: C−H Bond Activation and Non‐Classical Binding Modes at Boron.
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- Angewandte Chemie, 2022, v. 134, n. 7, p. 1, doi. 10.1002/ange.202112342
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Selective C−N Borylation of Alkyl Amines Promoted by Lewis Base.
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- Angewandte Chemie, 2018, v. 130, n. 46, p. 15447, doi. 10.1002/ange.201809608
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Lewis Acid Promoted Single C-F Bond Activation of the CF<sub>3</sub> Group: S<sub>N</sub>1′-Type 3,3-Difluoroallylation of Arenes with 2-Trifluoromethyl-1-alkenes.
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- Angewandte Chemie, 2017, v. 129, n. 21, p. 5984, doi. 10.1002/ange.201701985
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Accessing Frustrated Lewis Pair Chemistry from a Spectroscopically Stable and Classical Lewis Acid‐Base Adduct.
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- Angewandte Chemie, 2018, v. 130, n. 20, p. 5983, doi. 10.1002/ange.201802385
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Self-Assembled Nanocomposite Organic Polymers with Aluminum and Scandium as Heterogeneous Water-Compatible Lewis Acid Catalysts.
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- Angewandte Chemie, 2015, v. 127, n. 36, p. 10705, doi. 10.1002/ange.201503874
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Self-Assembled Nanocomposite Organic Polymers with Aluminum and Scandium as Heterogeneous Water-Compatible Lewis Acid Catalysts.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 36, p. 10559, doi. 10.1002/anie.201503874
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Reactivity of (β-Diketiminato)zinc Hydride toward Lewis Bases, Heterocumulenes and Cyclohexene Oxide.
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- European Journal of Inorganic Chemistry, 2012, v. 2012, n. 23, p. 3725, doi. 10.1002/ejic.201200378
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