Works matching DE "LEWIS bases"
Results: 732
Anti-Markovnikov hydroallylation reaction of alkenes via scandium-catalyzed allylic C‒H activation.
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- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-56602-6
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Contact ion-pair S<sub>N</sub>2 reactions activated by Lewis Base Phase transfer catalysts.
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- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-024-55795-6
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Electrolytic cleaning study of cold rolled steel using scanning Kelvin probe.
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- Surface Engineering, 2022, v. 38, n. 5, p. 499, doi. 10.1080/02670844.2022.2101416
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Synergistic Gold(I)/Trimethylsilyl Catalysis: Efficient Alkynylation of N,O-Acetals and Related Pro-Electrophiles.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 9, p. 2040, doi. 10.1002/adsc.201400169
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Stereoselective Lewis Base-Catalyzed Asymmetric Hydrosilylation of α-Acetamido-β-enamino Esters: Straightforward Approach for the Construction of α,β-Diamino Acid Derivatives.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 10, p. 1931, doi. 10.1002/adsc.201300184
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Usanovich and Nernst colliding: inconsistencies in the all-in-one acid–base concept?
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- Foundations of Chemistry, 2024, v. 26, n. 2, p. 197, doi. 10.1007/s10698-023-09482-x
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Hints for a formal language inspired by Lewis structures.
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- Foundations of Chemistry, 2022, v. 24, n. 3, p. 315, doi. 10.1007/s10698-022-09439-6
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Exploring an intermolecular Ge/B frustrated Lewis pair from a multicentre Zintl Lewis base.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2023, v. 142, n. 2, p. 1, doi. 10.1007/s00214-023-02961-6
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The mechanism studies of catalytic chemoselective conjugate addition of amino alcohols to α,β-unsaturated ester.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2021, v. 140, n. 1, p. 1, doi. 10.1007/s00214-020-02711-y
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The acid strength of the HClO<sub>4</sub>/<italic>n</italic>(AlF<sub>3</sub>) and HClO<sub>4</sub>/<italic>n</italic>(SbF<sub>5</sub>) (<italic>n </italic>= 1-3) Lewis-Brønsted superacids containing the excess of the Lewis acid component.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2018, v. 137, n. 4, p. 1, doi. 10.1007/s00214-018-2235-y
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Characterizing magnesium bonds: main features of a non-covalent interaction.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2017, v. 136, n. 3, p. 1, doi. 10.1007/s00214-017-2065-3
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On the thermodynamic stability of the intermolecular association between Lewis acids and Lewis bases: a DFT study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 3, p. 1, doi. 10.1007/s00214-016-1829-5
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The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties: Part 3. Catalysis of substitution, cycloaddition, isomerization, and rearrangement reactions.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 3, p. 265, doi. 10.1007/s10593-020-02655-y
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The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 2*. Catalysis of Michael and Biginelli reactions and nucleophilic addition at C=X and C≡X bonds.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 2, p. 145, doi. 10.1007/s10593-020-02637-0
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硫掺杂多孔碳材料的制备及其对脱硫废水中 重金属的电吸附性能研究.
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- Power Generation Technology, 2023, v. 43, n. 3, p. 382, doi. 10.12096/j.2096-4528.pgt.21128
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Improved Performance of Carbon Electrode Perovskite Solar Cells Using Urea Treatment in Two‐Step Processing.
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- ChemNanoMat, 2020, v. 6, n. 5, p. 806, doi. 10.1002/cnma.201900681
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Quadrupole correction for halogen bonding description in virtual screening and molecular docking.
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- Doklady Chemistry, 2016, v. 471, n. 1, p. 338, doi. 10.1134/S0012500816110100
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Peptide nucleic acid-zirconium coordination nanoparticles.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-40916-w
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Peptide nucleic acid-zirconium coordination nanoparticles.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-40916-w
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Hantzsch reaction using copper nitrate hydroxide-containing mesoporous silica nanoparticle with C<sub>3</sub>N<sub>4</sub> framework as a novel powerful and reusable catalyst.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-36059-7
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MODIFICAÇAO DA PERLITA EXPANDIDA COM ORTOFENANTROLINA PARA A FORMAÇAO DE SÍTIOS ATIVOS PARA CORANTES ÁCIDOS: PREPARAÇAO E CARACTERIZAÇAO.
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- Periódico Tchê Química, 2018, v. 15, n. 30, p. 338
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Evaluating the adhesive potential of the newly isolated bacterial strains in research exploitation of plant microbial interaction.
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- Frontiers in Plant Science, 2022, v. 13, p. 1, doi. 10.3389/fpls.2022.1004331
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Enantioconvergent construction of stereogenic silicon via Lewis base-catalyzed dynamic kinetic silyletherification of racemic chlorosilanes.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40558-6
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High-density frustrated Lewis pairs based on Lamellar Nb<sub>2</sub>O<sub>5</sub> for photocatalytic non-oxidative methane coupling.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37663-x
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The many faces of halogen bonding: a review of theoretical models and methods.
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- WIREs: Computational Molecular Science, 2014, v. 4, n. 6, p. 523, doi. 10.1002/wcms.1189
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Surface and Structural Modification of Nanostructured Mesoporous Silicon Oxycarbide Glasses Obtained from Preceramic Hybrids Aged in NH<sub>4</sub> OH.
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- Journal of the American Ceramic Society, 2013, v. 96, n. 1, p. 323, doi. 10.1111/jace.12000
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Organocatalytic Dynamic Kinetic Resolution: An Update.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 7, p. 1, doi. 10.1002/ejoc.202101561
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- Article
Synthesis and Evaluation of Enantiopure HMPA Analogs in Samarium‐Diiodide‐Promoted Dearomatizations of N‐Acylated Indole Derivatives.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 46, p. 6392, doi. 10.1002/ejoc.202101065
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Lewis Base-Catalyzed Cycloaddition of Heterocyclic Alkenes with 2,2,2-Trifluorodiazoethane (CF<sub>3</sub>CHN<sub>2</sub>): Access to Trifluoromethylated Pyrazolines and Pyrazoles.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 21, p. 2950, doi. 10.1002/ejoc.202100521
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Lewis Base‐Brønsted Acid Co‐catalyzed Morita‐Baylis‐Hillman Reaction of Cyclic Sulfamidate Imines.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 19, p. 2752, doi. 10.1002/ejoc.202100345
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Efficient Synthesis of 2-Amino-1-Arylethanols Through a Lewis Base-Catalyzed SiCl4-Mediated Asymmetric Passerini-Type Reaction.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 41, p. 6497, doi. 10.1002/ejoc.202001172
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The Effects of Structural Modifications of Bis‐tert‐alcohol‐Functionalized Crown‐Calix[4]arenes as Nucleophilic Fluorination Promotors and Relations with Computational Predictions.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 6, p. 728, doi. 10.1002/ejoc.201901746
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Cover Feature: Lewis Base Catalysis Promoted Nucleophilic Substitutions – Recent Advances and Future Directions (Eur. J. Org. Chem. 1/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 1, p. 4, doi. 10.1002/ejoc.201901798
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- Article
Lewis Base Catalysis Promoted Nucleophilic Substitutions – Recent Advances and Future Directions.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 1, p. 10, doi. 10.1002/ejoc.201901495
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Front Cover: Dehydrative Coupling of Benzylic Alcohols Catalyzed by Brønsted Acid/Lewis Base (Eur. J. Org. Chem. 34/2019).
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 34, p. 5828, doi. 10.1002/ejoc.201901233
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- Article
Dehydrative Coupling of Benzylic Alcohols Catalyzed by Brønsted Acid/Lewis Base.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 34, p. 5856, doi. 10.1002/ejoc.201900965
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- Article
Formal [2+2+1] Synthesis of Tetrasubstituted Furans from Aldehydes, Acetylenedicarboxylates, and Acyl Compounds.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 33, p. 5603, doi. 10.1002/ejoc.201900806
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- Article
Synthesis of Fused Indoline‐Cyclobutanone Derivatives via an Intramolecular [2+2] Cycloaddition.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 31/32, p. 5169, doi. 10.1002/ejoc.201900326
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Systematic Evaluation of Sulfoxides as Catalysts in Nucleophilic Substitutions of Alcohols.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 33, p. 4541, doi. 10.1002/ejoc.201800907
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- Article
Chiral Bisdiphenylphosphine Dioxides Bearing a Bis(triazolyl) Backbone as Promising Lewis Bases for Asymmetric Organocatalysis.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 19, p. 2267, doi. 10.1002/ejoc.201800317
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Lewis Base Promoted Reduction of CO<sub>2</sub> with BH<sub>3</sub>NH<sub>3</sub> into Boryl Formates: CO<sub>2</sub> as a Carbon Source in Organic Synthesis Under Mild Conditions.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 14, p. 1739, doi. 10.1002/ejoc.201800320
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Computational Study of the Cu-Free Allylic Alkylation Mechanism with Grignard Reagents: Role of the NHC Ligand.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 39, p. 5935, doi. 10.1002/ejoc.201701010
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Role of Lewis-Base-Coordinated Halogen(I) Intermediates in Organic Synthesis: The Journey from Unstable Intermediates to Versatile Reagents.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 37, p. 5497, doi. 10.1002/ejoc.201700916
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Lewis Acidities of Indol-3-ylmethylium Ions and Intrinsic Barriers of Their Reactions with Phosphines and Pyridines.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 23, p. 4050, doi. 10.1002/ejoc.201600572
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Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 12, p. 2110, doi. 10.1002/ejoc.201600286
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- Article
β-Lactams as Formal Dipoles through Amide-Bond Activation.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 3, p. 549, doi. 10.1002/ejoc.201501342
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- Article
Asymmetric Organocatalysis: The Emerging Utility of α,β-Unsaturated Acylammonium Salts.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 45, p. 13934, doi. 10.1002/anie.201602217
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Formamides as Lewis Base Catalysts in S<sub>N</sub> Reactions-Efficient Transformation of Alcohols into Chlorides, Amines, and Ethers.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 34, p. 10145, doi. 10.1002/anie.201604921
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Polymerization Initiated by Organic Electron Donors.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 20, p. 5994, doi. 10.1002/anie.201600327
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Thermal Dehydrogenation of Base-Stabilized B<sub>2</sub>H<sub>5</sub><sup>+</sup> Complexes and Its Role in CH Borylation.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 45, p. 13401, doi. 10.1002/anie.201507647
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