Works about HALOGENATION
Results: 754
Direct conversion of various phosphate sources to a versatile P-X reagent [TBA][PO<sub>2</sub>X<sub>2</sub>] via redox-neutral halogenation.
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- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-57255-1
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Biodegradation of 2,4,6-Tribromophenol by Ochrobactrum sp. Strain TB01.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 5, p. 1264, doi. 10.1271/bbb.70755
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Fluorination or Not in Small Molecule Solar Cells: Achieving a Higher Efficiency with Halogen‐Free End Group.
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- Chemistry - A European Journal, 2024, v. 30, n. 71, p. 1, doi. 10.1002/chem.202403341
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200 Years of The Haloform Reaction: Methods and Applications.
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- Chemistry - A European Journal, 2024, v. 30, n. 71, p. 1, doi. 10.1002/chem.202403045
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Controlling (E/Z)‐Stereoselectivity of −NHC=O Chlorination: Mechanism Principles for Wide Scope Applications.
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- Chemistry - A European Journal, 2024, v. 30, n. 60, p. 1, doi. 10.1002/chem.202400785
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Green Late‐Stage Functionalization of Tryptamines.
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- Chemistry - A European Journal, 2024, v. 30, n. 46, p. 1, doi. 10.1002/chem.202401436
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Telluronium‐Catalyzed Halogenation Reactions: Chalcogen‐Bond Activation of N‐Halosuccinimides and Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202401650
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Unspecific Peroxygenase (UPO) can be Tuned for Oxygenation or Halogenation Activity by Controlling the Reaction pH.
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- Chemistry - A European Journal, 2024, v. 30, n. 40, p. 1, doi. 10.1002/chem.202401706
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Enzymatic Resolution and Decarboxylative Functionalization of α‐Sulfinyl Esters.
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- Chemistry - A European Journal, 2024, v. 30, n. 7, p. 1, doi. 10.1002/chem.202302996
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Sunlight Induced and Alternative Sc(OTf)<sub>3</sub> Catalyzed Remote C−H Halogenation of Indoles.
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- Chemistry - A European Journal, 2023, v. 29, n. 36, p. 1, doi. 10.1002/chem.202300978
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Base‐Mediated Radio‐Iodination of Arenes by Using Organosilane and Organogermane as Radiolabelling Precursors.
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- Chemistry - A European Journal, 2023, v. 29, n. 19, p. 1, doi. 10.1002/chem.202203366
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Controlling the Flexibility of MIL‐88A(Sc) Through Synthetic Optimisation and Postsynthetic Halogenation.
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- Chemistry - A European Journal, 2022, v. 28, n. 48, p. 1, doi. 10.1002/chem.202201364
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Halogenation and Nucleophilic Quenching: Two Routes to E−X Bond Formation in Cobalt Triple‐Decker Complexes (E=As, P; X=F, Cl, Br, I).
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- Chemistry - A European Journal, 2022, v. 28, n. 43, p. 1, doi. 10.1002/chem.202201026
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Halogenation of the Hexaphosphabenzene Complex [(Cp*Mo)<sub>2</sub>(μ,η<sup>6</sup>:η<sup>6</sup>‐P<sub>6</sub>)]: Snapshots on the Reaction Progress.
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- Chemistry - A European Journal, 2022, v. 28, n. 32, p. 1, doi. 10.1002/chem.202200669
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Site‐Selective Distal C(sp<sup>3</sup>)−H Bromination of Aliphatic Amines as a Gateway for Forging Nitrogen‐Containing sp<sup>3</sup> Architectures.
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- Angewandte Chemie, 2024, v. 136, n. 33, p. 1, doi. 10.1002/ange.202406485
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Biosynthesis of Strained Amino Acids by a PLP‐Dependent Enzyme through Cryptic Halogenation.
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- Angewandte Chemie, 2024, v. 136, n. 31, p. 1, doi. 10.1002/ange.202319344
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On the Mechanisms of Hypohalous Acid Formation and Electrophilic Halogenation by Non‐Native Halogenases.
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- Angewandte Chemie, 2024, v. 136, n. 24, p. 1, doi. 10.1002/ange.202403858
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Triply Selective & Sequential Diversification at C<sub>sp</sub><sup>3</sup>: Expansion of Alkyl Germane Reactivity for C−C & C−Heteroatom Bond Formation.
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- Angewandte Chemie, 2024, v. 136, n. 16, p. 1, doi. 10.1002/ange.202401545
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Selective C−H Halogenation of Alkenes and Alkynes Using Flavin‐Dependent Halogenases.
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- Angewandte Chemie, 2024, v. 136, n. 13, p. 1, doi. 10.1002/ange.202317860
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The Influence of Donor/Acceptor Interfaces on Organic Solar Cells Efficiency and Stability Revealed through Theoretical Calculations and Morphology Characterizations.
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- Angewandte Chemie, 2024, v. 136, n. 10, p. 1, doi. 10.1002/ange.202318360
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Electrochemically Driven Nickel‐Catalyzed Halogenation of Unsaturated Halide and Triflate Derivatives.
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- Angewandte Chemie, 2024, v. 136, n. 2, p. 1, doi. 10.1002/ange.202311165
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Late‐Stage Halogenation of Peptides, Drugs and (Hetero)aromatic Compounds with a Nucleophilic Hydrazide Catalyst.
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- Angewandte Chemie, 2023, v. 135, n. 51, p. 1, doi. 10.1002/ange.202312597
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Photoredox‐Catalyzed Decarboxylative Bromination, Chlorination and Thiocyanation Using Inorganic Salts.
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- Angewandte Chemie, 2023, v. 135, n. 38, p. 1, doi. 10.1002/ange.202309684
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Symmetry‐Driven Assembly of a Penta‐Shell Keplerate Cuprofullerene for Metallofullerene Frameworks.
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- Angewandte Chemie, 2023, v. 135, n. 33, p. 1, doi. 10.1002/ange.202306748
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Heterogeneous Photocatalytic Recycling of FeX<sub>2</sub>/FeX<sub>3</sub> for Efficient Halogenation of C−H Bonds Using NaX.
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- Angewandte Chemie, 2023, v. 135, n. 23, p. 1, doi. 10.1002/ange.202302994
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Transition‐Metal‐Free Controllable Single and Double Difluoromethylene Formal Insertions into C−H Bonds of Aldehydes with TMSCF<sub>2</sub>Br.
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- Angewandte Chemie, 2023, v. 135, n. 7, p. 1, doi. 10.1002/ange.202217088
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The Single‐Component Flavin Reductase/Flavin‐Dependent Halogenase AetF is a Versatile Catalyst for Selective Bromination and Iodination of Arenes and Olefins.
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- Angewandte Chemie, 2022, v. 134, n. 51, p. 1, doi. 10.1002/ange.202214610
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Central Unit Fluorination of Non‐Fullerene Acceptors Enables Highly Efficient Organic Solar Cells with Over 18 % Efficiency.
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- Angewandte Chemie, 2022, v. 134, n. 41, p. 1, doi. 10.1002/ange.202209580
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Modular Halogenation, α‐Hydroxylation, and Acylation by a Remarkably Versatile Polyketide Synthase.
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- Angewandte Chemie, 2022, v. 134, n. 11, p. 1, doi. 10.1002/ange.202116614
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Catalytic Asymmetric Halogenation/Semipinacol Rearrangement of 3‐Hydroxyl‐3‐vinyl Oxindoles: A Stereodivergent Kinetic Resolution Process.
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- Angewandte Chemie, 2021, v. 133, n. 51, p. 26803, doi. 10.1002/ange.202110315
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Tuning the Circular Dichroism and Circular Polarized Luminescence Intensities of Chiral 2D Hybrid Organic–Inorganic Perovskites through Halogenation of the Organic Ions.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21604, doi. 10.1002/ange.202107239
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Recent Strategies for Carbon−Halogen Bond Formation Using Nickel.
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- Angewandte Chemie, 2021, v. 133, n. 31, p. 16888, doi. 10.1002/ange.202101324
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Photochemical Radical C–H Halogenation of Benzyl N‐Methyliminodiacetyl (MIDA) Boronates: Synthesis of α‐Functionalized Alkyl Boronates.
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- Angewandte Chemie, 2021, v. 133, n. 7, p. 3496, doi. 10.1002/ange.202011872
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Orthogonal Stability and Reactivity of Aryl Germanes Enables Rapid and Selective (Multi)Halogenations.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18876, doi. 10.1002/ange.202008372
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Frontispiz: Modulating Benzothiadiazole‐Based Covalent Organic Frameworks via Halogenation for Enhanced Photocatalytic Water Splitting.
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- Angewandte Chemie, 2020, v. 132, n. 39, p. 1, doi. 10.1002/ange.202083961
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Modulating Benzothiadiazole‐Based Covalent Organic Frameworks via Halogenation for Enhanced Photocatalytic Water Splitting.
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- Angewandte Chemie, 2020, v. 132, n. 39, p. 17050, doi. 10.1002/ange.202006925
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- Article
Pathway from N‐Alkylglycine to Alkylisonitrile Catalyzed by Iron(II) and 2‐Oxoglutarate‐Dependent Oxygenases.
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- Angewandte Chemie, 2020, v. 132, n. 19, p. 7437, doi. 10.1002/ange.201914896
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- Article
Nickel‐Catalyzed Conversion of Enol Triflates into Alkenyl Halides.
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- Angewandte Chemie, 2019, v. 131, n. 42, p. 15043, doi. 10.1002/ange.201906815
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- Article
Organoiodine‐Catalyzed Enantioselective Alkoxylation/Oxidative Rearrangement of Allylic Alcohols.
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- Angewandte Chemie, 2019, v. 131, n. 22, p. 7528, doi. 10.1002/ange.201903007
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The Chemical Properties of Hydrogen Atoms Adsorbed on M<sup>0</sup>‐Nanoparticles Suspended in Aqueous Solutions: The Case of Ag<sup>0</sup>‐NPs and Au<sup>0</sup>‐NPs Reduced by BD<sub>4</sub><sup>−</sup>.
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- Angewandte Chemie, 2018, v. 130, n. 50, p. 16763, doi. 10.1002/ange.201809302
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Rational Design of Organic Semiconductors for Texture Control and Self-Patterning on Halogenated Surfaces.
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- Advanced Functional Materials, 2014, v. 24, n. 32, p. 5052, doi. 10.1002/adfm.201400219
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Monte Carlo simulation study of the halogenated MIL-47(V) frameworks: influence of functionalization on HS adsorption and separation properties.
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- Journal of Materials Science, 2016, v. 51, n. 5, p. 2307, doi. 10.1007/s10853-015-9539-2
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- Article
Dioxobutanoic and 2-Arylamino-4-oxo-butenoic Acids.
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- Pharmaceutical Chemistry Journal, 2003, v. 37, n. 2, p. 71, doi. 10.1023/A:1024029525733
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Structure of 6,11-dichloro-9-dimethylthio-7,8-dicarba- nido-undecaborane [6,11-Cl-9-SMe-7,8-CBH].
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- Journal of Structural Chemistry, 2013, v. 54, n. 2, p. 349, doi. 10.1134/S0022476613020108
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Two-dimensional iodine-monofluoride epitaxy on WSe2.
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- NPJ 2D Materials & Applications, 2021, v. 5, n. 1, p. 1, doi. 10.1038/s41699-021-00201-8
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Synthesis of 3-Fluoro-Oxetane δ-Amino Acids.
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- Journal of Carbohydrate Chemistry, 2009, v. 28, n. 7/8, p. 431, doi. 10.1080/07328300903261562
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Synthesis of 2‐Deoxy‐2‐Fluoro‐2‐ C ‐Methyl‐D‐Ribofuranoses.
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- Journal of Carbohydrate Chemistry, 2006, v. 25, n. 6, p. 461, doi. 10.1080/07328300600859783
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Application of Electrochemical Processes to Classical Iodocyclisation: Utility for Selectivity and Mechanistic Insight.
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- ChemElectroChem, 2019, v. 6, n. 23, p. 5829, doi. 10.1002/celc.201901502
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Synthesis and structure-activity relationships of 2- and/or 4-halogenated 13β- and 13α-estrone derivatives as enzyme inhibitors of estrogen biosynthesis.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 1271, doi. 10.1080/14756366.2018.1490731
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Allergic contact dermatitis from budesonide.
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- Contact Dermatitis (01051873), 1993, v. 28, n. 2, p. 116, doi. 10.1111/j.1600-0536.1993.tb03358.x
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