Works matching DE "BORYLATION"
Results: 368
Methane functionalization by an Ir(III) catalyst supported on a metal–organic framework: an alternative explanation of steric confinement effects.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2019, v. 138, n. 9, p. N.PAG, doi. 10.1007/s00214-019-2498-y
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Ir-Catalyzed ortho -C-H Borylation of Aromatic C(sp 2)-H Bonds of Carbocyclic Compounds Assisted by N -Bearing Directing Groups.
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- Reactions (2624-781X), 2024, v. 5, n. 2, p. 318, doi. 10.3390/reactions5020016
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Moving from Fuel to Feedstock.
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- Johnson Matthey Technology Review, 2023, v. 67, n. 3, p. 333, doi. 10.1595/205651323X16765646706676
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Effective one-pot synthesis of (E)-poly(vinyl arylenes) via trans-borylation/Suzuki coupling protocol.
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- Green Processing & Synthesis, 2017, v. 6, n. 3, p. 301, doi. 10.1515/gps-2016-0217
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Stereospecific synthesis of silicon-stereogenic optically active silylboranes and general synthesis of chiral silyl Anions.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41113-z
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Arene C–H borylation strategy enabled by a non-classical boron cluster-based electrophile.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37258-6
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Iridium‐Catalyzed β‐C(sp<sup>2</sup>)−H Borylation of Enamides – Access to 3,3‐Dihalogeno‐2‐methoxypiperidines.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 2, p. 1, doi. 10.1002/ejoc.202101302
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Palladium‐Catalysed Carboborylation for the Synthesis of Borylated Indanes.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 29, p. 4072, doi. 10.1002/ejoc.202100309
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ω‐Alkenylallylboronates: Design, Synthesis, and Application to the Asymmetric Allylation/RCM Tandem Sequence.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 24, p. 3492, doi. 10.1002/ejoc.202100528
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Selective Vicinal Diiodination of Polycyclic Aromatic Hydrocarbons.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 36, p. 5847, doi. 10.1002/ejoc.202000954
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Synthesis of Biaryls Having a Piperidylmethyl Group Based on Space Integration of Lithiation, Borylation, and Suzuki–Miyaura Coupling.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 5, p. 618, doi. 10.1002/ejoc.201901729
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2,2‐Difluorovinyl Pinacolborane – A New Versatile Reagent for the Suzuki–Miyaura Reaction.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 37, p. 6417, doi. 10.1002/ejoc.201901118
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Preparation and Synthetic Applications of [2.2]Paracyclophane Trifluoroborates: An Efficient and Convenient Route to Nucleophilic [2.2]Paracyclophane Cross‐Coupling Building Blocks.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 36, p. 6198, doi. 10.1002/ejoc.201901171
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C‐H Activation/Metalation Approaches for the Synthesis of Indolizine Derivatives.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 31/32, p. 5205, doi. 10.1002/ejoc.201900608
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Synthesis of Raputimonoindoles A–C and Congeners.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 25, p. 4061, doi. 10.1002/ejoc.201900583
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Diverse Multi‐Functionalized Oligoarenes and Heteroarenes for Porous Crystalline Materials.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 7, p. 1446, doi. 10.1002/ejoc.201801232
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Decarboxylative Borylation: New Avenues for the Preparation of Organoboron Compounds.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 29, p. 3884, doi. 10.1002/ejoc.201800534
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Access to 1,1-Diborylalkenes and Concomitant Stereoselective Reactivity.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 22, p. 2728, doi. 10.1002/ejoc.201701786
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Vibrational Circular Dichroism Unveils Chiroptical, Electrical, and Magnetic Properties of Borylated Isocyanides and Aldehydes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 35, p. 5262, doi. 10.1002/ejoc.201701044
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Selective Borylation of [4]Helicene.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 34, p. 5647, doi. 10.1002/ejoc.201600979
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Front Cover: Selective Borylation of [4]Helicene (Eur. J. Org. Chem. 34/2016).
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 34, p. 5588, doi. 10.1002/ejoc.201670341
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Catalytic Friedel-Crafts C−H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 13, p. 3712, doi. 10.1002/anie.201611536
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Rhodium-Catalyzed Decarbonylative Borylation of Aromatic Thioesters for Facile Diversification of Aromatic Carboxylic Acids.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 9, p. 2482, doi. 10.1002/anie.201611974
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Catalytic Double Carbon-Boron Bond Formation for the Synthesis of Cyclic Diarylborinic Acids as Versatile Building Blocks for π-Extended Heteroarenes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 8, p. 2069, doi. 10.1002/anie.201612535
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Selective Cascade Reaction of Bisallenes via Palladium-Catalyzed Aerobic Oxidative Carbocyclization-Borylation and Aldehyde Trapping.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 6, p. 1590, doi. 10.1002/anie.201610524
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Lewis Acid-Base Interaction-Controlled ortho-Selective C−H Borylation of Aryl Sulfides.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 6, p. 1495, doi. 10.1002/anie.201610041
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A Chiral Nitrogen Ligand for Enantioselective, Iridium-Catalyzed Silylation of Aromatic C−H Bonds.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 4, p. 1092, doi. 10.1002/anie.201609939
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N-Heterocyclic Carbene Stabilized Boryl Radicals.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 4, p. 1135, doi. 10.1002/anie.201610903
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Diverse Visible-Light-Promoted Functionalizations of Benzotriazoles Inspired by Mechanism-Based Luminescence Screening.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 3, p. 902, doi. 10.1002/anie.201609393
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BCl<sub>3</sub>-Induced Annulative Oxo- and Thioboration for the Formation of C3-Borylated Benzofurans and Benzothiophenes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 1, p. 354, doi. 10.1002/anie.201610014
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Atom-Efficient Synthesis of Alkynylfluoroborates Using BF<sub>3</sub>-Based Frustrated Lewis Pairs.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 45, p. 14146, doi. 10.1002/anie.201608520
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A Boryl-Substituted Diphosphene: Synthesis, Structure, and Reaction with n-Butyllithium To Form a Stabilized Adduct by pπ-pπ Interaction.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 41, p. 12827, doi. 10.1002/anie.201607995
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Nickel-Catalyzed Decarbonylative Borylation of Amides: Evidence for Acyl C−N Bond Activation.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 30, p. 8718, doi. 10.1002/anie.201603068
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Palladium-Catalyzed Oxidative Carbocyclization-Borylation of Enallenes to Cyclobutenes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 22, p. 6520, doi. 10.1002/anie.201601613
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Ligand-Promoted Borylation of C(sp³)-H Bonds with Palladium(II)Catalysts.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 2, p. 785, doi. 10.1002/anie.201509996
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Efficient Synthesis of Formyl Boronate Esters Derived from Carbazole and Phenoxazine as Key Electron Donors.
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- Polycyclic Aromatic Compounds, 2022, v. 42, n. 10, p. 7178, doi. 10.1080/10406638.2021.1996410
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The Improved para -Selective C(sp 2)-H Borylation of Anisole Derivatives Enabled by Bulky Lewis Acid.
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- Catalysts (2073-4344), 2023, v. 13, n. 8, p. 1193, doi. 10.3390/catal13081193
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Masuda Borylation–Suzuki Coupling (MBSC) Sequence: A One-Pot Process to Access Complex (hetero)Biaryls.
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- Catalysts (2073-4344), 2023, v. 13, n. 2, p. 350, doi. 10.3390/catal13020350
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Synthesis of Novel Key Chromophoric Intermediates via C-C Coupling Reactions.
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- Catalysts (2073-4344), 2022, v. 12, n. 10, p. 1292, doi. 10.3390/catal12101292
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Layered Double Hydroxides as Bifunctional Catalysts for the Aryl Borylation under Ligand-Free Conditions.
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- Catalysts (2073-4344), 2019, v. 9, n. 4, p. 302, doi. 10.3390/catal9040302
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Suzuki–Miyaura Coupling Using Monolithic Pd Reactors and Scaling-Up by Series Connection of the Reactors.
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- Catalysts (2073-4344), 2019, v. 9, n. 3, p. 300, doi. 10.3390/catal9030300
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Borole Ring Expansion Reactions with Boron Azides: A Versatile Pathway to Borylated Azaborinines.
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- European Journal of Inorganic Chemistry, 2024, v. 27, n. 36, p. 1, doi. 10.1002/ejic.202400498
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One-Pot Palladium-Catalyzed Cross-Coupling Treble of Borylation, the Suzuki Reaction and Amination.
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- Advanced Synthesis & Catalysis, 2017, v. 359, n. 4, p. 616, doi. 10.1002/adsc.201600708
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Nickel-Catalyzed Borylation of Aryl and Benzyl 2-Pyridyl Ethers: A Method for Converting a Robust ortho-Directing Group.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 15, p. 2417, doi. 10.1002/adsc.201600336
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Synthesis of Enantiomerically Enriched Chiral Tetrahydroquinolines via Sequential Dearomatization/Enantioselective Borylation Reactions.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 15, p. 2379, doi. 10.1002/adsc.201600372
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- Article
α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu 3 (BTC) 2 Using Cesium Carbonate as a Base.
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- Nanomaterials (2079-4991), 2021, v. 11, n. 6, p. 1396, doi. 10.3390/nano11061396
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Nickel-catalyzed, silyl-directed, ortho-borylation of arenes via an unusual Ni(II)/Ni(IV) catalytic cycle.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51997-0
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Dinuclear gold-catalyzed divergent dechlorinative radical borylation of gem-dichloroalkanes.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-48085-8
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Trialkoxysilane-Induced Iridium-Catalyzed para-Selective C–H Bond Borylation of Arenes.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47205-8
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Enantioselective synthesis of (R)-tolterodine using lithiation/borylation–protodeboronation methodology.
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- Canadian Journal of Chemistry, 2012, v. 90, n. 11, p. 965, doi. 10.1139/v2012-069
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