Works matching DE "INDOLINONE"
Results: 65
Highly Regioselective Synthesis of Substituted Isoindolinones via Ruthenium-Catalyzed Alkyne Cyclotrimerizations.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 11/12, p. 2353, doi. 10.1002/adsc.201300055
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Synthesis and biological activity evaluation of 3-(hetero) arylideneindolin-2-ones as potential c-Src inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 2382, doi. 10.1080/14756366.2022.2117317
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Synthesis and biological evaluation of certain hydrazonoindolin-2-one derivatives as new potent anti-proliferative agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 867, doi. 10.1080/14756366.2018.1462802
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Novel [(3-indolylmethylene)hydrazono]indolin-2-ones as apoptotic anti-proliferative agents: design, synthesis and in vitro biological evaluation.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 686, doi. 10.1080/14756366.2017.1421181
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TBHP Mediated Substrate Controlled Oxidative Dearomatization of Indoles to C2/C3-Quaternary Indolinones.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 22, p. 2762, doi. 10.1002/ejoc.201800167
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Efficient Synthesis of Highly Functionalized Spirocarbocyclic Oxindoles through Hauser Annulation.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 37, p. 5689, doi. 10.1002/ejoc.201701023
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Ugi Reaction Followed by Intramolecular Diels-Alder Reaction and Elimination of HCl: One-Pot Approach to Arene-Fused Isoindolinones.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 30, p. 4379, doi. 10.1002/ejoc.201700747
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Asymmetric Synthesis of Quaternary β-Perfluorophenyl-β-amino-indolin-2-ones.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 11, p. 1540, doi. 10.1002/ejoc.201601645
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Bi(OTf)<sub>3</sub>-Catalysed Access to 2,3-Substituted Isoindolinones and Tricyclic N,O-Acetals by Trapping of Bis- N-Acyliminium Species in a Tandem Process.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 21, p. 3592, doi. 10.1002/ejoc.201600530
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Crystal and Molecular Structural Features of Indolin-2-One Derivatives with Sterically Hindered Phenol Moieties.
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- Journal of Structural Chemistry, 2018, v. 59, n. 2, p. 439, doi. 10.1134/S0022476618020270
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One-Pot Synthesis of Dihydroxyindeno[1,2-d]Imidazoles and Naphthoquinone Substituted Indandione and Oxindole Derivatives.
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- Polycyclic Aromatic Compounds, 2023, v. 43, n. 2, p. 1693, doi. 10.1080/10406638.2022.2033801
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Synthesis and intramolecular cyclization of some derivatives of 3-[(2,3-dihydro-1 Н-1,5-benzodiazepin-4-yl)methylidene]indolin-2-one.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 11, p. 1657, doi. 10.1134/S107042801611018X
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Synthesis and Antimicrobial Evaluation of Some New Spiroindolinone Derivatives.
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- Journal of Heterocyclic Chemistry, 2015, v. 52, n. 5, p. 1488, doi. 10.1002/jhet.2253
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Quaternary Ammonium Salt-Promoted Multi-Component Reaction in Water: Access to 3-Alkyl-2, 3-Dihydro-1H-Isoindolin-1-One Derivatives.
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- Advanced Synthesis & Catalysis, 2017, v. 359, n. 1, p. 146, doi. 10.1002/adsc.201600944
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Tandem C( sp<sup>3</sup>)−H Arylation/Oxidation and Arylation/Allylic Substitution of Isoindolinones.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 17, p. 2829, doi. 10.1002/adsc.201600654
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Isatis tinctoria L. (Woad): A Review of Its Botany, Ethnobotanical Uses, Phytochemistry, Biological Activities, and Biotechnological Studies.
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- Plants (2223-7747), 2020, v. 9, n. 3, p. 298, doi. 10.3390/plants9030298
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Copper-catalyzed oxidative trimerization of indoles by using TEMPO to construct quaternary carbon centers: the synthesis of 2-(1 H-indol-3-yl)-2,3′-biindolin-3-ones.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 4, p. 269, doi. 10.1139/cjc-2013-0435
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Copper (cat) and phenylboronic acid mediated deformylative C-N coupling of isoindolinone-3-ols with formamides provide C(3) aminoisoindolinones.
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- Journal of Chemical Sciences, 2018, v. 130, n. 6, p. 1, doi. 10.1007/s12039-018-1474-8
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Novel hydroxamic acids incorporating 1-((1H-1,2,3-Triazol-4-yl)methyl)-3-hydroxyimino-indolin-2-ones: synthesis, biological evaluation, and SAR analysis.
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- Journal of Chemical Sciences, 2018, v. 130, n. 6, p. 1, doi. 10.1007/s12039-018-1472-x
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Investigation of the reaction of 3-aroylmethylene-indol-2-ones with 2-hydrazinobenzothiazole.
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- Journal of Chemical Sciences, 2013, v. 125, n. 2, p. 299, doi. 10.1007/s12039-013-0364-3
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Catalyst-Free Three-Component Tandem CDC Cyclization: Convenient Access to Isoindolinones from Aromatic Acid, Amides, and DMSO by a Pummerer-Type Rearrangement.
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- Chemistry - A European Journal, 2016, v. 22, n. 18, p. 6262, doi. 10.1002/chem.201600865
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Asymmetric Synthesis of Fluorinated Isoindolinones through Palladium-Catalyzed Carbonylative Amination of Enantioenriched Benzylic Carbamates.
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- Chemistry - A European Journal, 2015, v. 21, n. 32, p. 11579, doi. 10.1002/chem.201500773
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Palladium-Catalyzed Carbonylation of 2-Bromoanilines with 2-Formylbenzoic Acid and 2-Halobenzaldehydes: Efficient Synthesis of Functionalized Isoindolinones.
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- Chemistry - A European Journal, 2014, v. 20, n. 44, p. 14184, doi. 10.1002/chem.201404446
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(E)-3-(Aryl(arylamino)methylene)indolin-2-one derivatives: an efficient synthetic approach and evaluation of their cancer inhibitory activity.
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- Journal of Chemical Research, 2018, v. 42, n. 1, p. 44, doi. 10.3184/174751918X15166485941737
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Chemoselective double Michael addition: synthesis of 2,6-diarylspiro[cyclohexane-1,3'-indoline]-2',4-diones via addition of indolin-2-one to divinyl ketones.
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- Journal of Chemical Research, 2017, v. 41, n. 3, p. 168, doi. 10.3184/174751917X14878812592779
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New Terpendole Congeners, Inhibitors of Sterol O-Acyltransferase, Produced by Volutella citrinella BF-0440.
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- Molecules, 2020, v. 25, n. 13, p. 3079, doi. 10.3390/molecules25133079
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Design, Synthesis and Preliminary Biological Evaluation of Novel Benzyl Sulfoxide 2-Indolinone Derivatives as Anticancer Agents.
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- Molecules, 2017, v. 22, n. 11, p. 1979, doi. 10.3390/molecules22111979
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New spiroindolinones bearing 5-chlorobenzothiazole moiety.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 4, p. 457, doi. 10.3109/14756366.2013.800058
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Phenylimino Indolinone: A Green‐Light‐Responsive T‐Type Photoswitch Exhibiting Negative Photochromism.
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- Angewandte Chemie, 2021, v. 133, n. 48, p. 25494, doi. 10.1002/ange.202111748
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Catalytic Enantioselective Aminopalladation–Heck Cascade.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7169, doi. 10.1002/ange.202016001
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Heteroannulation of Arynes with α‐Amino Imides: Synthesis of 2,2‐Disubstituted Indolin‐3‐ones and Application to the Enantioselective Total Synthesis of (+)‐Hinckdentine A.
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- Angewandte Chemie, 2018, v. 130, n. 20, p. 5781, doi. 10.1002/ange.201800746
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New chelating agents for Cu(II), Fe(III), Al(III), and Zn(II) based on β-diketonate-3-substituted phthalide (isobenzofuranone) and isoindolinone.
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- Journal of Coordination Chemistry, 2014, v. 67, n. 13, p. 2217, doi. 10.1080/00958972.2014.939075
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3D-QSAR Study on a Series of VEGFR-2 Kinase Inhibitors: 3-Pyrrole Substituted Indolin-2-Ones Compounds.
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- Journal of Chemistry, 2013, p. 1, doi. 10.1155/2013/374804
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Synthesis of mono and bis-[3,3-di(indolyl)indolin-2-ones] and evaluation of their antimicrobial activity.
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- Research on Chemical Intermediates, 2015, v. 41, n. 12, p. 10007, doi. 10.1007/s11164-015-2007-4
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- Article
Asymmetric Alkynylation/Lactamization Cascade: An Expeditious Entry to Enantiomerically Enriched Isoindolinones.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 40, p. 10737, doi. 10.1002/anie.201405074
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- Article
Use of a Readily Removable Auxiliary Group for the Synthesis of Pyrrolidones by the Palladium-Catalyzed Intramolecular Amination of Unactivated γ C(sp<sup>3</sup>)H Bonds.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 42, p. 11124, doi. 10.1002/anie.201305615
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One-pot green synthesis of biologically relevant novel spiro[indolin-2-one-3,4′-pyrano[2,3- c]pyrazoles] and studies on their spectral and X-ray crystallographic behaviors.
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- Acta Crystallographica Section B: Structural Science, Crystal Engineering & Materials, 2016, v. 72, n. 3, p. 335, doi. 10.1107/S2052520616005060
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Oxidative Asymmetric Aza-Friedel-Crafts Alkylation of Indoles with 3-Indolinone-2-carboxylates Catalyzed by a BINOL Phosphoric Acid and Promoted by DDQ.
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- Chemistry - An Asian Journal, 2018, v. 13, n. 10, p. 1327, doi. 10.1002/asia.201800300
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Multicomponent Synthesis of Isoindolinone Frameworks via Rh<sup>III</sup>‐Catalysed in situ Directing Group‐Assisted Tandem Oxidative Olefination/Michael Addition.
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- Chemistry - An Asian Journal, 2018, v. 13, n. 7, p. 765, doi. 10.1002/asia.201800120
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Nickel-Catalyzed Oxidative C−H/N−H Isocyanide Insertion: An Efficient Synthesis of Iminoisoindolinone Derivatives.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 11, p. 1664, doi. 10.1002/asia.201600193
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Effects on thrombocytic hemostasis of a new derivate indolinone.
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- Bangladesh Journal of Medical Science, 2019, v. 18, n. 3, p. 574, doi. 10.3329/bjms.v18i3.41628
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The Indolinone MAZ51 Induces Cell Rounding and G2/M Cell Cycle Arrest in Glioma Cells without the Inhibition of VEGFR-3 Phosphorylation: Involvement of the RhoA and Akt/GSK3β Signaling Pathways.
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- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0109055
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A study of the planarity of the pyrrolone fragment in 2-isopropyl-2,3-dihydro-1H-isoindol-1-one.
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- Acta Crystallographica Section C: Structural Chemistry, 2016, v. 72, n. 7, p. 518, doi. 10.1107/S2053229616008767
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- Article
Visible Light‐Mediated C2‐Quaternarization of N‐Alkyl Indoles through Oxidative Dearomatization using Ir(III) Catalyst.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 12, p. 2243, doi. 10.1002/ajoc.201900604
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- Article
One-Pot Synthesis of 3-Iminoisoindolinones by a Rhodium(III)-Catalyzed and Methanol-Assisted C−H Cyanation-Cyclization Cascade with N-Alkoxyl Transfer.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 11, p. 1250, doi. 10.1002/ajoc.201500294
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Microwave-assisted synthesis of isoindolinones via Pd-mediated tandem coupling reactions.
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- Heterocyclic Communications, 2018, v. 24, n. 3, p. 129, doi. 10.1515/hc-2018-0029
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Catalytic Enantioselective Synthesis of Mariline A and Related Isoindolinones through a Biomimetic Approach.
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- Angewandte Chemie, 2017, v. 129, n. 48, p. 15555, doi. 10.1002/ange.201709182
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Total Synthesis of (−)- N-Methylwelwitindolinone B Isothiocyanate.
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- Angewandte Chemie, 2017, v. 129, n. 33, p. 10094, doi. 10.1002/ange.201705322
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- Article
Dual Catalysis for the Redox Annulation of Nitroalkynes with Indoles: Enantioselective Construction of Indolin-3-ones Bearing Quaternary Stereocenters.
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- Angewandte Chemie, 2015, v. 127, n. 38, p. 11357, doi. 10.1002/ange.201504697
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- Article
Asymmetric Alkynylation/Lactamization Cascade: An Expeditious Entry to Enantiomerically Enriched Isoindolinones.
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- Angewandte Chemie, 2014, v. 126, n. 40, p. 10913, doi. 10.1002/ange.201405074
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- Article