Works matching DE "OXINDOLES"
Results: 478
Alkenyl oxindole is a novel PROTAC moiety that recruits the CRL4<sup>DCAF11</sup> E3 ubiquitin ligase complex for targeted protein degradation.
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- PLoS Biology, 2024, v. 22, n. 5, p. 1, doi. 10.1371/journal.pbio.3002550
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Enantioselective Synthesis of 3‐Hydroxy‐2‐Oxindoles via Ni‐Catalyzed Asymmetric Addition of Aromatic Bromides to α‐Ketoamides.
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- Chemistry - A European Journal, 2024, v. 30, n. 72, p. 1, doi. 10.1002/chem.202403622
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Regioselective Electrochemical Construction of C<sub>sp2</sub>−C<sub>sp2</sub> Linkage at C5−C5' Position of 2‐Oxindoles via an Intermolecular Anodic Dehydrogenative Coupling.
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- Chemistry - A European Journal, 2024, v. 30, n. 70, p. 1, doi. 10.1002/chem.202403420
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Photoinduced Metal‐Free Decarboxylative Fluoroalkylation of Alkenes for the Synthesis of N‐Arylbutanamides and Oxindoles.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402891
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Stable Axially Chiral Cyclohexylidenes from Catalytic Asymmetric Knoevenagel Condensation.
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- Chemistry - A European Journal, 2024, v. 30, n. 39, p. 1, doi. 10.1002/chem.202401243
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Hauser‐Kraus Annulation Initiated Multi‐Cascade Reactions for Facile Access to Functionalized and Fused Oxazepines, Carbazoles and Phenanthridinediones.
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- Chemistry - A European Journal, 2024, v. 30, n. 3, p. 1, doi. 10.1002/chem.202303517
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Asymmetric Rubottom‐Type Oxidation Catalyzed by Chiral Calcium Phosphates.
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- Chemistry - A European Journal, 2023, v. 29, n. 10, p. 1, doi. 10.1002/chem.202203720
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Experimental and Theoretical Investigation of an Azaoxyallyl Cation‐Templated Intramolecular Aryl Amination Leading to Oxindole Derivatives.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202201208
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Titelbild: Visible‐Light‐Induced Photoreduction of Carborane Phosphonium Salts: Efficient Synthesis of Carborane‐Oxindole‐Pharmaceutical Hybrids (Angew. Chem. 31/2023).
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202307360
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Photochemical Deracemization of 3‐Substituted Oxindoles.
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- Angewandte Chemie, 2023, v. 135, n. 30, p. 1, doi. 10.1002/ange.202305274
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Morphological Profiling Identifies the Motor Protein Eg5 as Cellular Target of Spirooxindoles.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202301955
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Stereodivergent Construction of Csp<sup>3</sup>−Csp<sup>3</sup> Bonds Bearing Vicinal Stereocenters by Synergistic Palladium and Phase‐Transfer Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 2, p. 1, doi. 10.1002/ange.202215714
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Multicomponent Assembly of Complex Oxindoles by Enantioselective Cooperative Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 51, p. 1, doi. 10.1002/ange.202213407
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Mechanochemical Divergent Syntheses of Oxindoles and α‐Arylacylamides via Controllable Construction of C−C and C−N Bonds by Copper and Piezoelectric Materials.
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- Angewandte Chemie, 2022, v. 134, n. 34, p. 1, doi. 10.1002/ange.202206420
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Bioinspired and Ligand‐Regulated Unnatural Prenylation and Geranylation of Oxindoles with Isoprene under Pd Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 32, p. 1, doi. 10.1002/ange.202207202
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Asymmetric Redox Allylic Alkylation to Access 3,3′‐Disubstituted Oxindoles Enabled by Ni/NHC Cooperative Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 22, p. 1, doi. 10.1002/ange.202201678
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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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Iron‐Catalyzed Reductive Cyclization by Hydromagnesiation: A Modular Strategy Towards N‐Heterocycles.
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- Angewandte Chemie, 2021, v. 133, n. 41, p. 22519, doi. 10.1002/ange.202106996
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A Unified Catalytic Asymmetric (4+1) and (5+1) Annulation Strategy to Access Chiral Spirooxindole‐Fused Oxacycles.
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- Angewandte Chemie, 2021, v. 133, n. 36, p. 19966, doi. 10.1002/ange.202105282
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Counterion Control of t‐BuO‐Mediated Single Electron Transfer to Nitrostilbenes to Construct N‐Hydroxyindoles or Oxindoles.
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- Angewandte Chemie, 2021, v. 133, n. 35, p. 19356, doi. 10.1002/ange.202104319
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Cycloisomerization of Carbamoyl Chlorides in Hexafluoroisopropanol: Stereoselective Synthesis of Chlorinated Methylene Oxindoles and Quinolinones.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18626, doi. 10.1002/ange.202103323
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Asymmetric Catalytic Vinylogous Addition Reactions Initiated by Meinwald Rearrangement of Vinyl Epoxides.
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- Angewandte Chemie, 2021, v. 133, n. 26, p. 14642, doi. 10.1002/ange.202102054
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Asymmetric Carbene‐Catalyzed Oxidation of Functionalized Aldimines as 1,4‐Dipoles.
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- Angewandte Chemie, 2021, v. 133, n. 14, p. 7992, doi. 10.1002/ange.202017017
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Photochemically Induced Ring Opening of Spirocyclopropyl Oxindoles: Evidence for a Triplet 1,3‐Diradical Intermediate and Deracemization by a Chiral Sensitizer.
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- Angewandte Chemie, 2020, v. 132, n. 48, p. 21824, doi. 10.1002/ange.202008384
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Palladium‐Catalyzed Enantioselective Heck Carbonylation with a Monodentate Phosphoramidite Ligand: Asymmetric Synthesis of (+)‐Physostigmine, (+)‐Physovenine, and (+)‐Folicanthine.
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- Angewandte Chemie, 2020, v. 132, n. 29, p. 12297, doi. 10.1002/ange.202003288
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P<sup>III</sup>/P<sup>V</sup>=O Catalyzed Cascade Synthesis of N‐Functionalized Azaheterocycles.
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- Angewandte Chemie, 2020, v. 132, n. 11, p. 4535, doi. 10.1002/ange.201914851
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Pd/Cu‐Catalyzed Enantioselective Sequential Heck/Sonogashira Coupling: Asymmetric Synthesis of Oxindoles Containing Trifluoromethylated Quaternary Stereogenic Centers.
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- Angewandte Chemie, 2020, v. 132, n. 7, p. 2786, doi. 10.1002/ange.201913148
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Hai‐Chao Xu.
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- Angewandte Chemie, 2019, v. 131, n. 49, p. 17668, doi. 10.1002/ange.201907300
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Enantioselective Synthesis of 2‐Oxindole Spirofused Lactones and Lactams by Heck/Carbonylative Cylization Sequences: Method Development and Applications.
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- Angewandte Chemie, 2019, v. 131, n. 27, p. 9323, doi. 10.1002/ange.201904838
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Asymmetric Allylic Alkylation with Deconjugated Carbonyl Compounds: Direct Vinylogous Umpolung Strategy.
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- Angewandte Chemie, 2019, v. 131, n. 27, p. 9308, doi. 10.1002/ange.201903478
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Enantioselective Synthesis of C−N Axially Chiral N‐Aryloxindoles by Asymmetric Rhodium‐Catalyzed Dual C−H Activation.
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- Angewandte Chemie, 2019, v. 131, n. 20, p. 6804, doi. 10.1002/ange.201901619
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Taming Radical Intermediates for the Construction of Enantioenriched Trifluoromethylated Quaternary Carbon Centers.
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- Angewandte Chemie, 2019, v. 131, n. 5, p. 1461, doi. 10.1002/ange.201812793
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Synthesis of Spirooxindoles: Compounds of Wide Therapeutical Applications.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 4, p. 288, doi. 10.1007/s11094-014-1096-5
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The synthesis of new oxindoles as analogs of natural product 3,3' -bis(indolyl)oxindole and in vitro evaluation of the enzyme activity of G6PD and 6PGD.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 332, doi. 10.3906/kim-1706-51
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Synthesis of new oxindole derivatives containing benzothiazole and thiazolidinone moieties using nano silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (NSB-DBU) as catalyst.
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- Turkish Journal of Chemistry, 2015, v. 39, n. 2, p. 235, doi. 10.3906/kim-1408-26
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Design and synthesis of thiazolidine-2/4-diones hybrids with 1,2-dihydroquinolones and 2-oxindoles as potential VEGFR-2 inhibitors: in-vitro anticancer evaluation and in-silico studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1903, doi. 10.1080/14756366.2022.2085693
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One-pot three-component synthesis of novel spirooxindoles with potential cytotoxic activity against triple-negative breast cancer MDA-MB-231 cells.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 309, doi. 10.1080/14756366.2017.1417276
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Synthesis, characterization and in vitro antimicrobial evaluation of new compounds incorporating oxindole nucleus.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 4, p. 599, doi. 10.3109/14756366.2011.576251
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Double Spirocyclization of Arylidene-Δ 2 -Pyrrolin-4-Ones with 3-Isothiocyanato Oxindoles.
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- Catalysts (2073-4344), 2020, v. 10, n. 10, p. 1211, doi. 10.3390/catal10101211
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Nano-rod ZnO as a novel and reusable catalyst for C-P bond formation and hydrophosphonation of isatin derivatives under solvent-free conditions.
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- Canadian Journal of Chemistry, 2013, v. 91, n. 11, p. 1117, doi. 10.1139/cjc-2011-0432
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Proton-bound complex mediating retro-Michael-type fragmentation of protonated 3-substituted oxindoles in the Orbitrap high-energy collisional dissociation cell.
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- Rapid Communications in Mass Spectrometry: RCM, 2015, v. 29, n. 6, p. 515, doi. 10.1002/rcm.7128
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Stereodivergent Construction of 1,5/1,7‐Nonadjacent Tetrasubstituted Stereocenters Enabled by Pd/Cu‐Cocatalyzed Asymmetric Heck Cascade Reaction.
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- Angewandte Chemie, 2024, v. 136, n. 35, p. 1, doi. 10.1002/ange.202407498
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Enantioseparation and racemization of 3‐fluorooxindoles.
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- Chirality, 2023, v. 35, n. 9, p. 619, doi. 10.1002/chir.23572
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Urea derivative organocatalyzed enantioselective Friedel–Crafts alkylation of α‐naphthols with isatins.
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- Chirality, 2022, v. 34, n. 7, p. 977, doi. 10.1002/chir.23447
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Candida antarctica lipase‐B‐catalyzed kinetic resolution of 1,3‐dialkyl‐3‐hydroxymethyl oxindoles.
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- Chirality, 2020, v. 32, n. 12, p. 1377, doi. 10.1002/chir.23284
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Direct Asymmetric anti-Mannich-Type Reactions Catalyzed by Cinchona Alkaloid Derivatives.
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- Chirality, 2014, v. 26, n. 12, p. 801, doi. 10.1002/chir.22358
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Asymmetric Pd-NHC<sup>*</sup>-catalyzed coupling reactions.
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- Pure & Applied Chemistry, 2012, v. 84, n. 8, p. 1741, doi. 10.1351/PAC-CON-12-02-10
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Enantioselective Synthesis of Spirooxindole Enols: Regioselective and Asymmetric [3+2] Cyclization of 3-Isothiocyanato Oxindoles with Dibenzylidene Ketones.
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- ChemistryOpen, 2016, v. 5, n. 4, p. 311, doi. 10.1002/open.201600034
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Design, synthesis, and discovery of novel oxindoles bearing 3-heterocycles as species-specific and combinatorial agents in eradicating Staphylococcus species.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-44304-1
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Unnatural spirocyclic oxindole alkaloids biosynthesis in Uncaria guianensis.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47706-3
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