Works matching DE "ARYL bromides"
Results: 345
Transition‐Metal Free Amination and Hydrodefluorination of Aryl Fluorides Promoted by Solvated Electrons.
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- Chemistry - A European Journal, 2024, v. 30, n. 70, p. 1, doi. 10.1002/chem.202403410
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Photomediated Hexafluoroisopropoxylation of Unactivated Aryl Halides.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402811
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Indole Nucleophile Triggers Mechanistic Divergence in Ni‐Photoredox N‐Arylation.
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- Chemistry - A European Journal, 2024, v. 30, n. 67, p. 1, doi. 10.1002/chem.202402524
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Introduction of Molecular Complexity via the Cross‐Coupling of Lithium 1,4‐Dioxene with Aryl Bromides.
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- Chemistry - A European Journal, 2024, v. 30, n. 61, p. 1, doi. 10.1002/chem.202402351
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Nickel‐Catalyzed Enantioselective Carbonyl Addition of Aryl Chlorides and Bromides to Aldehydes.
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- Chemistry - A European Journal, 2024, v. 30, n. 47, p. 1, doi. 10.1002/chem.202401591
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Synthesis of (Hetero)biaryls via Nickel Catalyzed Reductive Cross‐Electrophile Coupling Between (Hetero)aryl Iodides and Bromides.
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- Chemistry - A European Journal, 2024, v. 30, n. 44, p. 1, doi. 10.1002/chem.202401552
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Photoredox‐Catalyzed Preparation of Sulfones Using Bis‐Piperidine Sulfur Dioxide – An Underutilized Reagent for SO<sub>2</sub> Transfer.
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- Chemistry - A European Journal, 2024, v. 30, n. 12, p. 1, doi. 10.1002/chem.202303976
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Cover Feature: Carbonylation as a Key Step in New Tandem Reactions – A Route to BODIPYs (Chem. Eur. J. 9/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 9, p. 1, doi. 10.1002/chem.202400146
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A Nickel Anchored Covalent Organic Framework as Unimolecular Metallaphotocatalyst for Visible Light Driver C−P Bond Coupling Reaction.
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- Chemistry - A European Journal, 2024, v. 30, n. 9, p. 1, doi. 10.1002/chem.202303556
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Micelle‐Mediated Sonogashira Coupling for DNA‐Encoded Library Synthesis.
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- Chemistry - A European Journal, 2023, v. 29, n. 42, p. 1, doi. 10.1002/chem.202300603
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Copper‐Catalyzed Stereoselective Borylation and Palladium‐Catalyzed Stereospecific Cross‐Coupling to Give Aryl C‐Glycosides.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203376
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Overclocking Nitronyl Nitroxide Gold Derivatives in Cross‐Coupling Reactions.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203118
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Multistep Continuous Flow Synthesis of Isolable NH<sub>2</sub>‐Sulfinamidines via Nucleophilic Addition to Transient Sulfurdiimide.
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- Chemistry - A European Journal, 2022, v. 28, n. 59, p. 1, doi. 10.1002/chem.202202066
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Nickel‐Catalysed Cross‐Electrophile Coupling of Benzyl Bromides and Sulfonium Salts towards the Synthesis of Dihydrostilbenes.
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- Chemistry - A European Journal, 2022, v. 28, n. 54, p. 1, doi. 10.1002/chem.202201644
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Rhodium‐Catalyzed Direct ortho‐Arylation of Anilines.
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- Angewandte Chemie, 2024, v. 136, n. 30, p. 1, doi. 10.1002/ange.202403553
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Electro/Ni Dual‐Catalyzed Decarboxylative C(sp<sup>3</sup>)−C(sp<sup>2</sup>) Cross‐Coupling Reactions of Carboxylates and Aryl Bromide.
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- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202403844
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Room‐Temperature Copper‐Catalyzed Etherification of Aryl Bromides.
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- Angewandte Chemie, 2024, v. 136, n. 19, p. 1, doi. 10.1002/ange.202400333
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Copper‐Catalyzed α‐Arylation of Nitroalkanes with (Hetero)aryl Bromides/Iodides.
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- Angewandte Chemie, 2024, v. 136, n. 7, p. 1, doi. 10.1002/ange.202315994
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Mechanistic Evidence of a Ni(0/II/III) Cycle for Nickel Photoredox Amide Arylation.
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- Angewandte Chemie, 2023, v. 135, n. 43, p. 1, doi. 10.1002/ange.202310753
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Haohua Huo.
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- Angewandte Chemie, 2023, v. 135, n. 33, p. 1, doi. 10.1002/ange.202308402
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Metallaphotoredox‐Catalyzed Enantioselective Cross‐Electrophile Coupling Using Alcohols as Reducing Agents.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202305889
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β‐Arylation of Racemic Secondary Benzylic Alcohols to Access Enantioenriched β‐Arylated Alcohols.
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- Angewandte Chemie, 2023, v. 135, n. 30, p. 1, doi. 10.1002/ange.202306015
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Catalytic S<sub>N</sub>Ar Hexafluoroisopropoxylation of Aryl Chlorides and Bromides.
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- Angewandte Chemie, 2023, v. 135, n. 24, p. 1, doi. 10.1002/ange.202302908
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Closing the Cycle as It Begins: Synthesis of ortho‐Iodobiaryls via Catellani Reaction.
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- Angewandte Chemie, 2023, v. 135, n. 18, p. 1, doi. 10.1002/ange.202218928
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Synthesis of P‐Stereogenic Phosphine Oxides via Nickel‐Catalyzed Asymmetric Cross‐Coupling of Secondary Phosphine Oxides with Alkenyl and Aryl Bromides.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202300011
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Nickel‐Catalyzed Cross‐Electrophile 1,2‐Silyl‐Arylation of 1,3‐Dienes with Chlorosilanes and Aryl Bromides.
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- Angewandte Chemie, 2023, v. 135, n. 4, p. 1, doi. 10.1002/ange.202215703
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Photo‐Excited Nickel‐Catalyzed Silyl‐Radical‐Mediated Direct Activation of Carbamoyl Chlorides To Access (Hetero)aryl Carbamides.
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- Angewandte Chemie, 2022, v. 134, n. 44, p. 1, doi. 10.1002/ange.202207472
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Cu‐Catalyzed Coupling Reactions of Sulfonamides with (Hetero)Aryl Chlorides/Bromides.
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202210483
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[Ph<sub>4</sub>P]<sup>+</sup>[Cu(CF<sub>2</sub>H)<sub>2</sub>]<sup>−</sup>: A Powerful Difluoromethylating Reagent Inspired by Mechanistic Investigation.
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- Angewandte Chemie, 2022, v. 134, n. 42, p. 1, doi. 10.1002/ange.202210151
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Scalable, Chemoselective Nickel Electrocatalytic Sulfinylation of Aryl Halides with SO<sub>2</sub>.
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- Angewandte Chemie, 2022, v. 134, n. 37, p. 1, doi. 10.1002/ange.202208080
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Diazaphospholene‐Catalyzed Radical Reactions from Aryl Halides**.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202204088
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Acridine‐Functionalized Covalent Organic Frameworks (COFs) as Photocatalysts for Metallaphotocatalytic C−N Cross‐Coupling.
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- Angewandte Chemie, 2022, v. 134, n. 21, p. 1, doi. 10.1002/ange.202117738
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gem‐Difluoroallylation of Aryl Halides and Pseudo Halides with Difluoroallylboron Reagents in High Regioselectivity.
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- Angewandte Chemie, 2021, v. 133, n. 49, p. 25950, doi. 10.1002/ange.202111476
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Base‐Activated Latent Heteroaromatic Sulfinates as Nucleophilic Coupling Partners in Palladium‐Catalyzed Cross‐Coupling Reactions.
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- Angewandte Chemie, 2021, v. 133, n. 41, p. 22635, doi. 10.1002/ange.202109146
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Radical 1,4‐Aryl Migration Enabled Remote Cross‐Electrophile Coupling of α‐Amino‐β‐Bromo Acid Esters with Aryl Bromides.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21530, doi. 10.1002/ange.202106273
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Palladium/TY‐Phos‐Catalyzed Asymmetric Intermolecular α‐Arylation of Aldehydes with Aryl Bromides.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18690, doi. 10.1002/ange.202106109
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Electrochemical Generation of Hypervalent Bromine(III) Compounds.
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- Angewandte Chemie, 2021, v. 133, n. 29, p. 15966, doi. 10.1002/ange.202104677
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Nickel‐Catalyzed Asymmetric Reductive Carbo‐Carboxylation of Alkenes with CO<sub>2</sub>.
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- Angewandte Chemie, 2021, v. 133, n. 25, p. 14187, doi. 10.1002/ange.202102769
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Scalable Negishi Coupling between Organozinc Compounds and (Hetero)Aryl Bromides under Aerobic Conditions when using Bulk Water or Deep Eutectic Solvents with no Additional Ligands.
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- Angewandte Chemie, 2021, v. 133, n. 19, p. 10726, doi. 10.1002/ange.202101571
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Diverse Synthesis of Chiral Trifluoromethylated Alkanes via Nickel‐Catalyzed Asymmetric Reductive Cross‐Coupling Fluoroalkylation.
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- Angewandte Chemie, 2021, v. 133, n. 18, p. 10035, doi. 10.1002/ange.202101076
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Oxalohydrazide Ligands for Copper‐Catalyzed C−O Coupling Reactions with High Turnover Numbers.
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- Angewandte Chemie, 2021, v. 133, n. 15, p. 8284, doi. 10.1002/ange.202015654
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Assembly of α‐(Hetero)aryl Nitriles via Copper‐Catalyzed Coupling Reactions with (Hetero)aryl Chlorides and Bromides.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7158, doi. 10.1002/ange.202014638
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Cross‐Coupling between Hydrazine and Aryl Halides with Hydroxide Base at Low Loadings of Palladium by Rate‐Determining Deprotonation of Bound Hydrazine.
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- Angewandte Chemie, 2021, v. 133, n. 1, p. 403, doi. 10.1002/ange.202011161
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Tandem Photoredox Catalysis: Enabling Carbonylative Amidation of Aryl and Alkylhalides.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18805, doi. 10.1002/ange.202006720
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Enantioselective Preparation of Arenes with β‐Stereogenic Centers: Confronting the 1,1‐Disubstituted Olefin Problem Using CuH/Pd Cooperative Catalysis.
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- Angewandte Chemie, 2020, v. 132, n. 37, p. 16262, doi. 10.1002/ange.202004414
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Light-Promoted Nickel Catalysis: Etherification of Aryl Electrophiles with Alcohols Catalyzed by a Ni<sup>II</sup>-Aryl Complex.
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- Angewandte Chemie, 2020, v. 132, n. 31, p. 12814, doi. 10.1002/ange.202003359
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General Paradigm in Photoredox Nickel‐Catalyzed Cross‐Coupling Allows for Light‐Free Access to Reactivity.
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- Angewandte Chemie, 2020, v. 132, n. 24, p. 9614, doi. 10.1002/ange.201916398
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Berichtigung: Palladium(I) Dimer Enabled Extremely Rapid and Chemoselective Alkylation of Aryl Bromides over Triflates and Chlorides in Air.
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- Angewandte Chemie, 2020, v. 132, n. 20, p. 7715, doi. 10.1002/ange.202002528
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Synthesis and Functionalization of Allenes by Direct Pd‐Catalyzed Organolithium Cross‐Coupling.
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- Angewandte Chemie, 2020, v. 132, n. 20, p. 7897, doi. 10.1002/ange.201913132
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Regioselective Hydroalkylation and Arylalkylation of Alkynes by Photoredox/Nickel Dual Catalysis: Application and Mechanism.
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- Angewandte Chemie, 2020, v. 132, n. 14, p. 5787, doi. 10.1002/ange.201914061
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