Works matching DE "ISATIN"
Results: 593
Photoinduced Redox Cascade Reaction of Isatins and Aliphatic Carboxylic Acids to Access 6‐Hydroxyindoloquinazolinones.
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- Chemistry - A European Journal, 2024, v. 30, n. 51, p. 1, doi. 10.1002/chem.202400655
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Goldkatalysierte formale [4+2]‐Cycloaddition als Zugang zu antitumoraktiven spirozyklischen Oxindolen aus Alkinen und von Isatin abgeleiteten Ketiminen.
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- Angewandte Chemie, 2023, v. 135, n. 34, p. 1, doi. 10.1002/ange.202304672
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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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Asymmetric Allylation by Chiral Organocatalyst‐Promoted Formal Hetero‐Ene Reactions of Alkylgold Intermediates.
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- Angewandte Chemie, 2021, v. 133, n. 4, p. 2020, doi. 10.1002/ange.202012678
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Catalytic Enantioselective Ynamide Additions to Isatins: Concise Access to Oxindole Alkaloids.
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- Angewandte Chemie, 2019, v. 131, n. 11, p. 3440, doi. 10.1002/ange.201814074
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Assessment of 5-substituted Isatin as Surface Recognition Group: Design, Synthesis, and Antiproliferative Evaluation of Hydroxamates as Novel Histone Deacetylase Inhibitors.
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- Pharmaceutical Chemistry Journal, 2017, v. 51, n. 5, p. 366, doi. 10.1007/s11094-017-1616-1
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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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Synthesis, characterization, and in vitro antimicrobial evaluation of hydrazone and bishydrazone derivatives of isatin.
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- Pharmaceutical Chemistry Journal, 2010, v. 44, n. 4, p. 219, doi. 10.1007/s11094-010-0436-3
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Synthesis and Structure of Hybrid Compounds Based on Phosphoryl Acetic Acid Hydrazide, Isatin, and Sterically Hindered Phenols.
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- Journal of Structural Chemistry, 2019, v. 60, n. 11, p. 1804, doi. 10.1134/S0022476619110143
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Crystal structure of a Mn(II) complex with isatin-hydrazone-S-benzyldithiocarbazate.
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- Journal of Structural Chemistry, 2014, v. 55, n. 1, p. 130, doi. 10.1134/S0022476614010211
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Amplified Anodic Electrogenerated Chemiluminescence of Tris(2,2′‐bipyridyl)ruthenium(II) for the Sensitive Detection of Isatin.
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- ChemElectroChem, 2020, v. 7, n. 5, p. 1207, doi. 10.1002/celc.201902148
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Synthesis biological evaluation and molecular docking of isatin hybrids as anti-cancer and anti-microbial agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2024, v. 39, n. 1, p. 1, doi. 10.1080/14756366.2023.2288548
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Evaluation of N-alkyl isatins and indoles as acetylcholinesterase and butyrylcholinesterase inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2024, v. 39, n. 1, p. 1, doi. 10.1080/14756366.2023.2286935
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Identification of sulphonamide-tethered N-((triazol-4-yl)methyl)isatin derivatives as inhibitors of SARS-CoV-2 main protease.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2234665
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Discovery of sulfonamide-tethered isatin derivatives as novel anticancer agents and VEGFR-2 inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2203389
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Synthesis and bioevaluation of novel steroidal isatin conjugates derived from epiandrosterone/androsterone.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1607, doi. 10.1080/14756366.2019.1659790
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Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 130, doi. 10.1080/14756366.2016.1238366
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Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 68, doi. 10.1080/14756366.2016.1235042
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Insights into the mechanism of inhibition of tryptophan 2,3-dioxygenase by isatin derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 70, doi. 10.3109/14756366.2016.1170013
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Synthesis and anti-inflammatory activity evaluation of novel triazolyl-isatin hybrids.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1520, doi. 10.3109/14756366.2016.1151015
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Inhibitory effects of isatin Mannich bases on carbonic anhydrases, acetylcholinesterase, and butyrylcholinesterase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1498, doi. 10.3109/14756366.2016.1149479
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5-Nitroisatin-derived thiosemicarbazones: potential antileishmanial agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 5, p. 628, doi. 10.3109/14756366.2013.836641
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Synthesis of a new class of antimicrobial agents incorporating the indolin-2-one moiety.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 4, p. 853, doi. 10.3109/14756366.2012.689298
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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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Antiproliferative effects of metal complexes of new isatin hydrazones against HCT116, MCF7 and HELA tumour cell lines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 3, p. 330, doi. 10.3109/14756366.2011.588950
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Synthesis, characterization and biocidal activity of some transition metal(II) complexes with isatin salicylaldehyde acyldihydrazones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 3, p. 319, doi. 10.3109/14756366.2011.588228
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Synthesis, anticancer and antioxidant activities of some novel N-(benzo[d]oxazol-2-yl)-2-(7- or 5-substituted-2-oxoindolin-3-ylidene) hydrazinecarboxamide derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2011, v. 26, n. 6, p. 813, doi. 10.3109/14756366.2011.556630
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Template synthesis of macrocyclic complexes and their spectroscopic and antibacterial studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2010, v. 25, n. 3, p. 445, doi. 10.3109/14756360903190754
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Metal based isatin-derived sulfonamides: Their synthesis, characterization, coordination behavior and biological activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2009, v. 24, n. 3, p. 859, doi. 10.1080/14756360802447636
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In vitro cytotoxic, antibacterial, antifungal and urease inhibitory activities of some N4- substituted isatin-3-thiosemicarbazones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2008, v. 23, n. 6, p. 848, doi. 10.1080/14756360701746179
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Colorimetric Determination of 2-Chlorobenzylidene Malonitrile in Gases and Liquids.
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- Analytical Letters, 2023, v. 56, n. 11, p. 1856, doi. 10.1080/00032719.2022.2148684
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Synthesis and Biological Activity of Barbituric acid- linked Isatin Derivatives.
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- Egyptian Academic Journal of Biological Sciences, C Physiology & Molecular Biology, 2023, v. 15, n. 2, p. 11, doi. 10.21608/EAJBSC.2023.307820
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SBA-Pr-IS-MN-DM: a new fluorescent chemosensor for trace detection of silver in aqueous solutions.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-80406-1
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Catalytic Enantioselective Addition of Me<sub>2</sub>Zn to Isatins.
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- Catalysts (2073-4344), 2017, v. 7, n. 12, p. 387, doi. 10.3390/catal7120387
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The Prophylactic and Multimodal Activity of Two Isatin Thiosemicarbazones against Alzheimer's Disease In Vitro.
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- Brain Sciences (2076-3425), 2022, v. 12, n. 6, p. 806, doi. 10.3390/brainsci12060806
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A Computational Study of the Immobilization of New 5-Nitroisatine Derivatives with the Use of C60-Based Functionalized Nanocarriers.
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- Symmetry (20738994), 2023, v. 15, n. 1, p. 226, doi. 10.3390/sym15010226
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Facile and Convenient One-Pot Process for the Synthesis of Spirooxindole Derivatives in High Optical Purity Using (--)-(S)-Brevicolline as an Organocatalyst.
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- Symmetry (20738994), 2011, v. 3, n. 2, p. 165, doi. 10.3390/sym3020165
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Design, synthesis, docking, and antidepressant activity evaluation of isatin derivatives bearing Schiff bases.
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- Iranian Journal of Basic Medical Sciences, 2023, v. 26, n. 4, p. 438, doi. 10.22038/IJBMS.2023.68363.14916
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Synthesis of spiropyran derivatives over 1-(carboxymethyl) pyridinium iodide as nanostructured pyridinium salt under aqueous media.
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- Canadian Journal of Chemistry, 2017, v. 95, n. 2, p. 194, doi. 10.1139/cjc-2016-0374
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DABCO-functionalized mesoporous SBA-15: an efficient and recyclable catalyst for the synthesis of spiro-pyranoxindoles as antioxidant agents.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 12, p. 1163, doi. 10.1139/cjc-2014-0309
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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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Multi-component supramolecular synthesis of spirooxindoles catalyzed by β-cyclodextrin in water.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 12, p. 1704, doi. 10.1139/V09-137
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Ruthenium-catalyzed efficient routes to oxindole derivatives.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 9, p. 1213, doi. 10.1139/V09-098
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Reactions of 6-aminouracils — A novel and highly efficient procedure for preparation of some new spiro pyridodipyrimidines under classical or microwave-assisted solvent-free conditions.
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- Canadian Journal of Chemistry, 2008, v. 86, n. 9, p. 925, doi. 10.1139/V08-117
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Synthesis and Spectroscopic Analysis of Schiff Bases of Imesatin and Isatin Derivatives.
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- Journal of Applied Sciences & Environmental Management, 2016, v. 20, n. 3, p. 653, doi. 10.4314/jasem.v20i3.20
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Spectroscopic, DNA cleavage and antimicrobial studies of Co(II), Ni(II) and Cu(II) complexes of sulfur donor Schiff bases.
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- Journal of Sulfur Chemistry, 2010, v. 31, n. 2, p. 109, doi. 10.1080/17415991003668186
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Chiroptical Sensing of Amines With Isatins.
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- Chirality, 2024, v. 36, n. 11, p. 1, doi. 10.1002/chir.70002
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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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Urea derivative catalyzed enantioselective aldol reaction of isatins with ketones.
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- Chirality, 2018, v. 30, n. 8, p. 1005, doi. 10.1002/chir.22977
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Enantioselective Aldol Reaction Between Isatins and Cyclohexanone Catalyzed by Amino Acid Sulphonamides.
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- Chirality, 2015, v. 27, n. 4, p. 314, doi. 10.1002/chir.22433
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