Works matching DE "CARBAZOLE derivatives"
Results: 200
Preparation of Carbazoles Involving 6π‐Electrocyclization, Photoredox‐, Electrochemical‐, and Thermal Cyclization Reactions: Mechanistic Insights.
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- Chemistry - A European Journal, 2024, v. 30, n. 8, p. 1, doi. 10.1002/chem.202303229
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Full‐Color Emissive D‐D‐A Carbazole Luminophores: Red‐to‐NIR Mechano‐fluorochromism, Aggregation‐Induced Near‐Infrared Emission, and Application in Photodynamic Therapy.
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- Chemistry - A European Journal, 2023, v. 29, n. 11, p. 1, doi. 10.1002/chem.202203797
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Front Cover: Full‐Color Emissive D‐D‐A Carbazole Luminophores: Red‐to‐NIR Mechano‐fluorochromism, Aggregation‐Induced Near‐Infrared Emission, and Application in Photodynamic Therapy (Chem. Eur. J. 11/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 11, p. 1, doi. 10.1002/chem.202300241
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Full‐Color Emissive D‐D‐A Carbazole Luminophores: Red‐to‐NIR Mechano‐fluorochromism, Aggregation‐Induced Near‐Infrared Emission, and Application in Photodynamic Therapy.
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- Chemistry - A European Journal, 2023, v. 29, n. 11, p. 1, doi. 10.1002/chem.202203797
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Bridging the Bays, Both Ways: A Janus Butterfly‐Shaped Intense NIR‐Emitting Terrylene Diimide.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202205600
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m-Indolocarbazole Derivative as a Universal Host Material for RGB and White Phosphorescent OLEDs.
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- Advanced Functional Materials, 2015, v. 25, n. 34, p. 5548, doi. 10.1002/adfm.201502079
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Conjugated microporous polymer-based carbazole derivatives as fluorescence chemosensors for picronitric acid.
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- Journal of Materials Science, 2016, v. 51, n. 8, p. 4104, doi. 10.1007/s10853-016-9732-y
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In silico Pharmacological Evaluation of Tetrahydro-β-carboline Derivatives as Putative Inhibitors of Alpha-Synuclein and Dopa Decarboxylase for Parkinson’s Disease.
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- Trends in Sciences, 2023, v. 20, n. 11, p. 1, doi. 10.48048/tis.2023.6008
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Progress in the chemistry of 3-amino-9-ethylcarbazole.
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- Turkish Journal of Chemistry, 2019, v. 43, n. 2, p. 369, doi. 10.3906/kim-1811-6
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Improvement of electrochemical and structural properties of polycarbazole by simultaneous electrodeposition of chitosan.
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- Turkish Journal of Chemistry, 2017, v. 41, n. 2, p. 233, doi. 10.3906/kim-1604-95
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Palindromic carbazole derivatives: unveiling their antiproliferative effect via topoisomerase II catalytic inhibition and apoptosis induction.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2024, v. 39, n. 1, p. 1, doi. 10.1080/14756366.2024.2302920
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Design, synthesis, and biological evaluation of novel carbazole derivatives as potent DNMT1 inhibitors with reasonable PK properties.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1537, doi. 10.1080/14756366.2022.2079640
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Design, synthesis and evaluation of carbazole derivatives as potential antimicrobial agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 296, doi. 10.1080/14756366.2020.1850713
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Synthesis and biological evaluation of novel N-(piperazin-1-yl)alkyl-1H-dibenzo[a,c]carbazole derivatives of dehydroabietic acid as potential MEK inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1544, doi. 10.1080/14756366.2019.1655407
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Carbazole scaffolds in cancer therapy: a review from 2012 to 2018.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1321, doi. 10.1080/14756366.2019.1640692
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N-thioalkylcarbazoles derivatives as new anti-proliferative agents: synthesis, characterisation and molecular mechanism evaluation.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 434, doi. 10.1080/14756366.2017.1419216
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Biologically active carbazole derivatives: focus on oxazinocarbazoles and related compounds.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 2, p. 180, doi. 10.3109/14756366.2014.899594
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Synthesis, antimicrobial activity and cytotoxicity of some new carbazole derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 6, p. 868, doi. 10.3109/14756366.2011.622273
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Fluorescence Sensors Based on Hydroxycarbazole for the Determination of Neurodegeneration-Related Halide Anions.
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- Biosensors (2079-6374), 2022, v. 12, n. 3, p. 175, doi. 10.3390/bios12030175
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Mini-review on the novel synthesis and potential applications of carbazole and its derivatives.
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- Designed Monomers & Polymers, 2023, v. 26, n. 1, p. 90, doi. 10.1080/15685551.2023.2194174
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Antiseptic Effects of New 3′- N-Substituted Carbazole Derivatives In Vitro and In Vivo.
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- Inflammation, 2015, v. 38, n. 4, p. 1649, doi. 10.1007/s10753-015-0141-1
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Heteropolyacid Catalyzed Synthesis Of Indole Derivatives Via Fischer Indole Synthesis.
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- Gazi University Journal of Science, 2011, v. 24, n. 4, p. 709
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2,3 : 6,7‐Naphthalene Bis(dicarboximide) Cyclophane: A Photofunctional Host for Ambient Delayed Fluorescence in Solution.
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- Angewandte Chemie, 2024, v. 136, n. 43, p. 1, doi. 10.1002/ange.202411102
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Degradation of carbazole, dibenzothiophene and polyaromatic hydrocarbons by recombinant Rhodococcus sp.
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- Biotechnology Letters, 2017, v. 39, n. 2, p. 277, doi. 10.1007/s10529-016-2242-9
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A computational study of the nonlinear optical properties of carbazole derivatives: theory refines experiment.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2014, v. 133, n. 4, p. 1, doi. 10.1007/s00214-014-1458-9
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Syntheses and photoluminescence properties of rhenium(I) complexes based on dipyrido[3,2-a:2',3'-c]phenazine derivatives with carbazole moiety.
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- Journal of Coordination Chemistry, 2013, v. 66, n. 5/6, p. 958, doi. 10.1080/00958972.2013.773427
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Repurposing anti-inflammatory drugs for fighting planktonic and biofilm growth. New carbazole derivatives based on the NSAID carprofen: synthesis, in silico and in vitro bioevaluation.
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- Frontiers in Cellular & Infection Microbiology, 2023, p. 1, doi. 10.3389/fcimb.2023.1181516
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Three-component diels-alder reaction through palladium carbene migratory insertion enabled dearomative C(sp<sup>3</sup>)-H bond activation.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-55190-1
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SYNTHESIS OF THIAZOLIDINE-CARBAZOLE LINKED 1,2,3-TRIAZOLE HYBRIDS AND THEIR ANTI-CANCER EVALUATION.
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- Rasayan Journal of Chemistry, 2021, v. 14, n. 3, p. 1551, doi. 10.31788/RJC.2021.1436249
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Highly Efficient and Stable Blue OLEDs Based on B—N Bonds Embedded 6,12‐Diphenyl‐5,11‐dihydroindolo[3,2‐b]carbazole with Narrowband Emission and Extended Lifetime<sup>†</sup>.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 6, p. 657, doi. 10.1002/cjoc.202200693
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Sesquicentennial birth anniversary of carbazole, a multifaceted wonder molecule: a revisit to its synthesis, photophysical and biological studies.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 6, p. 2075, doi. 10.1007/s13738-021-02444-0
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Effect of different acceptors on N-hexyl carbazole moiety for dye-sensitized solar cells: design, characterization, molecular structure, and DSSC fabrications.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 4, p. 949, doi. 10.1007/s13738-020-02082-y
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Pharmacophore interactions analysis and prediction of inhibitory activity of 1,7-diazacarbazoles as checkpoint kinase 1 inhibitors: application of molecular docking, 3D-QSAR and RBF neural network.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 6, p. 1525, doi. 10.1007/s13738-016-0869-z
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Direct synthesis of benzo[ a]carbazoles by palladium-catalyzed domino reactions: synthesis and photophysical properties of diverse benzo[ a]carbazoles.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 1, p. 7, doi. 10.1007/s13738-015-0706-9
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Structure-Property Relationship of New Organic Sensitizers Based on Multicarbazole Derivatives for Dye-Sensitized Solar Cells.
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- International Journal of Photoenergy, 2014, p. 1, doi. 10.1155/2014/872617
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Antimicrobial Potential of Carbazole Derivatives.
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- Croatica Chemica Acta, 2022, v. 95, n. 2, p. 39, doi. 10.5562/cca3899
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Distinguishing the Quantum Yield and Lifetime of Carbazole‐Based Room‐Temperature Phosphorescence Materials: QM/MM Study.
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- Annalen der Physik, 2022, v. 534, n. 12, p. 1, doi. 10.1002/andp.202200342
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A carbazole alkaloid deactivates mTOR through the suppression of rictor and that induces apoptosis in lung cancer cells.
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- Molecular & Cellular Biochemistry, 2015, v. 405, n. 1/2, p. 149, doi. 10.1007/s11010-015-2406-2
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Synthesis of novel carbazole hydrazine-carbothioamide scaffold as potent antioxidant, anticancer and antimicrobial agents.
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- BMC Chemistry, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s13065-024-01207-1
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Preparation and property analysis of antioxidant of carbazole derivatives.
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- BMC Chemistry, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s13065-024-01155-w
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Design, synthesis, molecular docking and biological evaluation of new carbazole derivatives as anticancer, and antioxidant agents.
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- BMC Chemistry, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s13065-023-00961-y
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Design, Synthesis and Biological Screening of Novel Carbazole Tethered Oxyethylamino Derivatives as Antimicrobial Agent.
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- Indian Journal of Pharmaceutical Education & Research, 2023, v. 57, p. s399, doi. 10.5530/ijper.57.2s.46
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IN SILICO DESIGNING AND SCREENING OF CARBAZOLE DERIVATIVES AS TOPOISOMERASE II INHIBITORS.
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- Indian Drugs, 2024, v. 61, n. 6, p. 21, doi. 10.53879/id.61.06.14226
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Synthesis and Properties of Fused Polycyclic Donor–Acceptor Compounds Containing Carbazole and Diazapyrene Skeletons.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 10, p. 1, doi. 10.1002/ajoc.202400289
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Pd‐Catalyzed Decarboxylative Cross‐Coupling of N‐Aryl Anthranilic Acids to Access Carbazoles: Gram Scale Total Synthesis of Anti‐ Cancer Drug Ellipticine.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 11, p. 1, doi. 10.1002/ajoc.202300429
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Tetra‐substituted Dipolar Carbazoles: Tuning Optical and Electroluminescence Properties by Linkage Variation.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 8, p. 1654, doi. 10.1002/ajoc.201800248
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Carbazole‐based dual‐functional chemosensor: Colorimetric sensor for Co<sup>2+</sup> and fluorescent sensor for Cu<sup>2+</sup> and its application.
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- Journal of the Chinese Chemical Society, 2021, v. 68, n. 12, p. 2368, doi. 10.1002/jccs.202100343
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Photophysical Properties of Emissive Pyrido[3,2‐c]carbazole Derivatives and Apoptosis Induction: Development towards Theranostic Agents in Response to Light Stimulus.
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- Chemistry - An Asian Journal, 2019, v. 14, n. 21, p. 3938, doi. 10.1002/asia.201901200
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Unique Solid-State Emission Behavior of Aromatic Difluoroboronated β-Diketones as an Emitter in Organic Light-Emitting Devices.
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- Chemistry - An Asian Journal, 2017, v. 12, n. 17, p. 2299, doi. 10.1002/asia.201700800
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Three-Arm, Biotin-Tagged Carbazole-Dicyanovinyl-Chlorambucil Conjugate: Simultaneous Tumor Targeting, Sensing, and Photoresponsive Anticancer Drug Delivery.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 24, p. 3482, doi. 10.1002/asia.201601264
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