Works about INDOLE
Results: 2430
Synthesis and Biological Activity of N-Acyl O-Indolylalkyl Ethanolamines.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 4, p. 768, doi. 10.1271/bbb.100804
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Evaluation and Target Validation of Indole Derivatives as Inhibitors of the AcrAB-To1C Efflux Pump.
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- Bioscience, Biotechnology & Biochemistry, 2010, v. 74, n. 11, p. 2237, doi. 10.1271/bbb.100433
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Novel Reactivity of Dibenzothiophene Monooxygenase from Bacillus subtilis WU-S2B.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 9, p. 2128, doi. 10.1271/bbb.90284
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Regioselectivity, of Larock Indole Synthesis Using Functionalized Alkynes.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 8, p. 2092, doi. 10.1271/bbb.80179
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Indole Derivatives Sustain Embryonic Stem Cell Self-Renewal in Long-Term Culture.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 5, p. 1242, doi. 10.1271/bbb.70717
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Quantification of Indole-3-Acetic Acid and Amino Acid Conjugates in Rice by Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 4, p. 778, doi. 10.1271/bbb.69.778
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Microbial Hydroxylation of Indole to 7-Hydroxyindole by Acinetobacter calcoaceticus Strain 4-1-5.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 5, p. 1167, doi. 10.1271/bbb.68.1167
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Oxidative Reaction of Oxindole-3-acetic Acids.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 9, p. 1870, doi. 10.1271/bbb.67.1870
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Secondary Sphere Lewis Acid Activated Heme Superoxo Adducts Mimic Crucial Non‐Covalent Interactions in IDO/TDO Heme Dioxygenases.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402310
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- Article
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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Synthesis of Indole‐Fused Pyrazino[1,2‐a]quinazolinones by Copper(I)‐Catalyzed Selective Hydroamination‐Cyclization of Alkynyl‐tethered Quinazolinones.
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- Chemistry - A European Journal, 2024, v. 30, n. 50, p. 1, doi. 10.1002/chem.202402085
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Cover Feature: Indole C5‐Selective Bromination of Indolo[2,3‐a]quinolizidine Alkaloids via In Situ‐Generated Indoline Intermediate (Chem. Eur. J. 35/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 35, p. 1, doi. 10.1002/chem.202401974
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Indole C5‐Selective Bromination of Indolo[2,3‐a]quinolizidine Alkaloids via In Situ‐Generated Indoline Intermediate.
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- Chemistry - A European Journal, 2024, v. 30, n. 35, p. 1, doi. 10.1002/chem.202401153
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B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>/CPA‐Catalyzed Aza‐Diels‐Alder Reaction of 3,3‐Difluoro‐2‐Aryl‐3H‐indoles and Unactivated Dienes.
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- Chemistry - A European Journal, 2024, v. 30, n. 34, p. 1, doi. 10.1002/chem.202401008
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Formation, Selective Encapsulation, and Tautomerization Control of Isoindolone Utilizing Guanidinium Sulfonate Frameworks.
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- Chemistry - A European Journal, 2024, v. 30, n. 33, p. 1, doi. 10.1002/chem.202400957
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Synthesis of Pyridazino[4,5‐b]indoles by [3+3] Annulation of 2‐Alkenylindoles and Hydrazonyl Chlorides.
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- Chemistry - A European Journal, 2024, v. 30, n. 26, p. 1, doi. 10.1002/chem.202400278
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Mechanochemical C−H Arylation and Alkylation of Indoles Using 3 d Transition Metal and Zero‐Valent Magnesium.
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- Chemistry - A European Journal, 2024, v. 30, n. 26, p. 1, doi. 10.1002/chem.202304231
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In2Q2: A New Entry of 16‐Membered Tetraazamacrocycle Concatenating Indole and Quinoline Units.
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- Chemistry - A European Journal, 2024, v. 30, n. 25, p. 1, doi. 10.1002/chem.202304176
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Palladium‐Catalyzed Carbonylation Reaction of Indole/Pyrrole Involving HCFO‐1233zd (E).
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- Chemistry - A European Journal, 2024, v. 30, n. 24, p. 1, doi. 10.1002/chem.202304056
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Designing Powerful Biindole‐Based Inherently Chiral Selectors: Enhancing Enantiodiscrimination by Core Functionalization with Additional Coordination Elements.
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- Chemistry - A European Journal, 2024, v. 30, n. 23, p. 1, doi. 10.1002/chem.202303530
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Divergent Electrochemical Synthesis of Indoles through pK<sub>a</sub> Regulation of Amides: Synthetic and Mechanistic Insights.
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- Chemistry - A European Journal, 2024, v. 30, n. 20, p. 1, doi. 10.1002/chem.202304002
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5‐Hydroxypyrroloindoline Affords Tryptathionine and 2,2′‐bis‐Indole Peptide Staples: Application to Melanotan‐II.
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- Chemistry - A European Journal, 2024, v. 30, n. 19, p. 1, doi. 10.1002/chem.202304270
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Rh‐Catalyzed Chemodivergent [3+3] Annulations of Diazoenals and α‐Aminoketones: Direct Synthesis of Functionalized 1,2‐Dihydropyridines and Fused 1,4‐Oxazines.
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- Chemistry - A European Journal, 2024, v. 30, n. 19, p. 1, doi. 10.1002/chem.202303862
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Transition‐Metal‐Free Synthesis of 2‐Substituted Benzo[cd]Indoles via the Reaction of 1‐Halo‐8‐lithionaphthalenes with Nitriles.
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- Chemistry - A European Journal, 2024, v. 30, n. 10, p. 1, doi. 10.1002/chem.202303768
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Ethynyl‐B(dan) in [3+2] Cycloaddition and Larock Indole Synthesis: Synthesis of Stable Boron‐Containing Heteroaromatic Compounds.
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- Chemistry - A European Journal, 2024, v. 30, n. 8, p. 1, doi. 10.1002/chem.202303403
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Highly Efficient Oxindole‐Based Molecular Photoswitches.
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- Chemistry - A European Journal, 2023, v. 29, n. 55, p. 1, doi. 10.1002/chem.202301634
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Molecular Editing Enhances Oxidation Resistance of Menaquinone‐Targeting Antibiotics Lysocin E and WAP‐8294A2.
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- Chemistry - A European Journal, 2023, v. 29, n. 47, p. 1, doi. 10.1002/chem.202301224
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Regioselective Dehydrogenative Reverse Prenylation of Indoles with 2‐Methyl‐2‐butene.
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- Chemistry - A European Journal, 2023, v. 29, n. 37, p. 1, doi. 10.1002/chem.202300933
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C--H Functionalization of Heterocycles with Triplet Carbenes by means of an Unexpected 1,2-Alkyl Radical Migration.
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- Chemistry - A European Journal, 2023, v. 29, n. 29, p. 1, doi. 10.1002/chem.202300214
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Highly Chemoselective Synthesis of Indole Derivatives.
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- Chemistry - A European Journal, 2023, v. 29, n. 28, p. 1, doi. 10.1002/chem.202300191
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Atroposelective Synthesis of Heterobiaryls through Ring Formation.
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- Chemistry - A European Journal, 2023, v. 29, n. 27, p. 1, doi. 10.1002/chem.202300183
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Front Cover: Atroposelective Nenitzescu Indole Synthesis (Chem. Eur. J. 25/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 25, p. 1, doi. 10.1002/chem.202300779
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Atroposelective Nenitzescu Indole Synthesis.
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- Chemistry - A European Journal, 2023, v. 29, n. 25, p. 1, doi. 10.1002/chem.202300279
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Chiral NHC‐Catalyzed [4+2] Cycloadditions: Highly Diastereo/Enantioselective Access to Spiro[cyclohex‐4‐ene‐1,3′‐indoles] and DFT Calculations.
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- Chemistry - A European Journal, 2023, v. 29, n. 23, p. 1, doi. 10.1002/chem.202203818
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Divergent Construction of N‐Doped Polycyclic Aromatic Hydrocarbons with Indole as the Nitrogen Source Building Block.
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- Chemistry - A European Journal, 2023, v. 29, n. 22, p. 1, doi. 10.1002/chem.202300140
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Indole‐Based Long‐Wavelength Fluorescent Probes for Bioimaging of S‐Nitrosylation in Mitochondria.
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- Chemistry - A European Journal, 2022, v. 28, n. 58, p. 1, doi. 10.1002/chem.202201494
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Decatungstate‐Photocatalyzed Dearomative Hydroacylation of Indoles: Direct Synthesis of 2‐Acylindolines.
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- Chemistry - A European Journal, 2022, v. 28, n. 56, p. 1, doi. 10.1002/chem.202201707
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Neutron Diffraction Study of Indole Solvation in Deep Eutectic Systems of Choline Chloride, Malic Acid, and Water.
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- Chemistry - A European Journal, 2022, v. 28, n. 41, p. 1, doi. 10.1002/chem.202200566
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Se‐(Fluoromethyl) Benzenesulfonoselenoates: Shelf‐Stable, Easily Available Reagents for Monofluoromethylselenolation.
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- Chemistry - A European Journal, 2022, v. 28, n. 39, p. 1, doi. 10.1002/chem.202200981
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Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines.
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- Chemistry - A European Journal, 2022, v. 28, n. 37, p. 1, doi. 10.1002/chem.202201113
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Late‐Stage Chemoenzymatic Installation of Hydroxy‐Bearing Allyl Moiety on the Indole Ring of Tryptophan‐Containing Peptides.
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- Chemistry - A European Journal, 2022, v. 28, n. 20, p. 1, doi. 10.1002/chem.202104614
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Discovery of (±)‐Penindolenes Reveals an Unusual Indole Ring Cleavage Pathway Catalyzed by P450 Monooxygenase.
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- Angewandte Chemie, 2024, v. 136, n. 26, p. 1, doi. 10.1002/ange.202403963
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Design and Catalytic Asymmetric Synthesis of Furan‐Indole Compounds Bearing both Axial and Central Chirality.
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- Angewandte Chemie, 2024, v. 136, n. 8, p. 1, doi. 10.1002/ange.202316454
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Discovery of Natural Potent HMG‐CoA Reductase Degraders for Lowering Cholesterol.
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- Angewandte Chemie, 2024, v. 136, n. 6, p. 1, doi. 10.1002/ange.202313859
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One‐Carbon Ring Expansion of Indoles and Pyrroles: A Straightforward Access to 3‐Fluorinated Quinolines and Pyridines.
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- Angewandte Chemie, 2024, v. 136, n. 5, p. 1, doi. 10.1002/ange.202317104
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Atroposelective Synthesis of Planar‐Chiral Indoles via Carbene Catalyzed Macrocyclization.
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- Angewandte Chemie, 2024, v. 136, n. 3, p. 1, doi. 10.1002/ange.202316739
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Tailored Design of π‐Extended Multi‐Resonance Organoboron using Indolo[3,2‐b]Indole as a Multi‐Nitrogen Bridge.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202313254
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Synthetic Matching of Complex Monoterpene Indole Alkaloid Chemical Space.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202310222
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Intermolecular Formal Cycloaddition of Indoles with Bicyclo[1.1.0]butanes by Lewis Acid Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202308606
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Asymmetric N‐Alkylation of 1H‐Indoles via Carbene Insertion Reaction.
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- Angewandte Chemie, 2023, v. 135, n. 47, p. 1, doi. 10.1002/ange.202313091
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