Works matching DE "PYRROLE derivatives"
Results: 442
Activation and C−C Coupling of Aryl Iodides via Bismuth Photocatalysis.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202418367
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Concise Total Synthesis of Acortatarin A.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 3, p. 676, doi. 10.1271/bbb.120862
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Benzodithiophene-Based Broad Absorbing Random Copolymers Incorporating Weak and Strong Electron Accepting Imide and Lactam Functionalized Pyrrolo[3,4-c]pyrrole Derivatives for Polymer Solar Cells.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 9, p. 996, doi. 10.1002/macp.201400614
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Oxidative [4+2] Annulation of Pyrrole‐2‐carbaldehyde Derivatives with o‐Hydroxyphenyl Propargylamines: Syntheses of 5,6,7‐Trisubstituted Indolizines.
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- Chemistry - A European Journal, 2024, v. 30, n. 63, p. 1, doi. 10.1002/chem.202402487
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Ion‐Pairing Assemblies of Anion‐Responsive π‐Electronic Systems That Have Noncovalently Assisted Expanded Planar Region.
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- Chemistry - A European Journal, 2024, v. 30, n. 49, p. 1, doi. 10.1002/chem.202401932
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Progress of Azametallacyclopentadienes in the New Century.
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- Chemistry - A European Journal, 2023, v. 29, n. 27, p. 1, doi. 10.1002/chem.202204079
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Red‐to‐Near‐Infrared Emitting PyrrolylBODIPY Dyes: Synthesis, Photophysical Properties and Bioimaging Application.
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- Chemistry - A European Journal, 2023, v. 29, n. 14, p. 1, doi. 10.1002/chem.202203832
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Chiral Calix[3]pyrrole Derivatives: Synthesis, Racemization Kinetics, and Ring Expansion to Calix[9]‐ and Calix[12]pyrrole Analogues.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202301460
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Heterocyclic Hemithioindigos: Highly Advantageous Properties as Molecular Photoswitches**.
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202210855
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Trifluoroethanol as a Unique Additive for the Chemoselective Electrooxidation of Enamines to Access Unsymmetrically Substituted NH‐Pyrroles.
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- Angewandte Chemie, 2022, v. 134, n. 5, p. 1, doi. 10.1002/ange.202111679
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Hydrolysis of Aliphatic Bis‐isonitriles in the Presence of a Polar Super Aryl‐Extended Calix[4]pyrrole Container.
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- Angewandte Chemie, 2021, v. 133, n. 18, p. 10447, doi. 10.1002/ange.202101499
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Dinuclear Triple‐Stranded Helicates Composed of Tetradentate Ligands with Aluminum(III) Chromophores: Optical Resolution and Multi‐color Circularly Polarized Luminescence Properties.
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- Angewandte Chemie, 2021, v. 133, n. 5, p. 2646, doi. 10.1002/ange.202011450
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Diastereodivergent Asymmetric 1,3‐Dipolar Cycloaddition of Azomethine Ylides and β‐Fluoroalkyl Vinylsulfones: Low Copper(II) Catalyst Loading and Theoretical Studies.
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- Angewandte Chemie, 2019, v. 131, n. 46, p. 16790, doi. 10.1002/ange.201908227
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Chemospecific Cyclizations of α‐Carbonyl Sulfoxonium Ylides on Aryls and Heteroaryls.
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- Angewandte Chemie, 2019, v. 131, n. 45, p. 16344, doi. 10.1002/ange.201910821
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Symmetrically functionalized diketopyrrolopyrrole with alkylated thiophene moiety: from synthesis to electronic devices applications.
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- Journal of Materials Science, 2014, v. 49, n. 12, p. 4215, doi. 10.1007/s10853-014-8116-4
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Synthesis and Cytotoxic Activity of Ethyl 2-Amino-1-Benzamido-4-Oxo-5-(2-Oxo-2-Arylethylidene)- 4,5-Dihydro-1 H-Pyrrole-3-Carboxylates.
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- Pharmaceutical Chemistry Journal, 2016, v. 49, n. 12, p. 817, doi. 10.1007/s11094-016-1378-1
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Synthesis and Antibacterial and Immunobiological Activity of Ethyl-1-(4-Aminosulfonylphenyl)-5-Aryl-3-Hydroxy-2-Oxo-3-Pyrroline-4-Carboxylates.
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- Pharmaceutical Chemistry Journal, 2016, v. 49, n. 10, p. 677, doi. 10.1007/s11094-016-1351-z
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Synthesis and Biological Activity of 5-aryl-4-acyl-3-hydroxy-1-(2-piperazin-1-ylethyl)-2,5-dihydropyrrol-2-ones and their Derivatives.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 9, p. 485, doi. 10.1007/s11094-013-0986-2
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STUDYING THE NATURE OF HYDROGEN BONDS OF H-COMPLEXES OF PYRROLE DERIVATIVES WITH ACETONE ACCORDING TO IR SPECTROSCOPY DATA AND QUANTUM CHEMICAL CALCULATIONS.
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- Journal of Structural Chemistry, 2021, v. 62, n. 5, p. 678, doi. 10.1134/S0022476621050036
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Experimental and theoretical studies of diethyl 2-( ter-butylimino)-2,5-dihydro-5-oxo-1-phenyl-1H-pyrrole-3,4-dicarboxylate using DFT calculations.
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- Journal of Structural Chemistry, 2017, v. 58, n. 7, p. 1341, doi. 10.1134/S0022476617070101
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Conformational and configurational diversity of solvent inclusion complexes of some calix[4]pyrroles and their anion recognition properties.
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- Journal of Structural Chemistry, 2015, v. 56, n. 7, p. 1379, doi. 10.1134/S0022476615070203
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Computational investigation of intramo lecular reorganization energy in diketopyrrolopyrrole (DPP) derivatives.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 3, p. 869, doi. 10.3906/kim-1711-21
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Electrochemical polymerization of a new alkoxy-bridged dithieno (3,2-B:2',3'-D) pyrrole derivative.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 439, doi. 10.3906/kim-1709-33
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Preparation and Characterization of Nanofilm-Coated Modified Electrodes and Their Use in Valsartan Drug Analysis.
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- Nanosistemi, Nanomateriali, Nanotehnologii, 2024, v. 22, n. 1, p. 197, doi. 10.15407/nnn.22.01.197
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Models of Nanostructures Based on Titanium Dioxide TiO2 for Transport of Biologically Active Compounds.
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- Nanosistemi, Nanomateriali, Nanotehnologii, 2020, v. 18, n. 4, p. 1077
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尼泊尔手工纸的热裂解特性分析.
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- China Pulp & Paper, 2024, v. 43, n. 10, p. 12, doi. 10.11980/j.issn.0254-508X.2024.10.002
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The Paal–Knorr Pyrroles Synthesis: A Green Perspective.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 5, p. 3558, doi. 10.1080/10406638.2023.2225676
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Activated Carbon and Zeolite Promoted Removing Aromatic Antibiotic Such as Cefixime and Amoxicillin from Aqueous Environment: Synthesis of Pyrrol Derivatives Using Amoxicillin.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 4, p. 2535, doi. 10.1080/10406638.2023.2219361
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Bio-ZnO/Fe<sub>3</sub>O<sub>4</sub>@MWCNTs Magnetic Nanocomposites Promoted Green Synthesis of Pyrrole Derivatives and Removal of Cefixime and Amoxiciline from Aqueous Solution.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 3, p. 1991, doi. 10.1080/10406638.2023.2210248
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Synthesis and antimicrobial activity of some new hydrazone-bridged thiazole-pyrrole derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 4, p. 830, doi. 10.3109/14756366.2012.688043
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Coordination Chemistry of Linear Tripyrroles: Promises and Perils.
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- Comments on Inorganic Chemistry, 2016, v. 36, n. 6, p. 327, doi. 10.1080/02603594.2016.1180291
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Novel Bifunctional Mesoporous Catalysts Based on Preyssler Heteropolyacids for Green Pyrrole Derivative Synthesis.
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- Catalysts (2073-4344), 2018, v. 8, n. 10, p. 419, doi. 10.3390/catal8100419
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N-Substituted Pyrrole Derivative 12m Inhibits HIV-1 Entry by Targeting Gp41 of HIV-1 Envelope Glycoprotein.
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- Frontiers in Pharmacology, 2019, p. 1, doi. 10.3389/fphar.2019.00859
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Roles of reactive oxygen species in UVA-induced oxidation of 5,6-dihydroxyindole-2-carboxylic acid-melanin as studied by differential spectrophotometric method.
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- Pigment Cell & Melanoma Research, 2016, v. 29, n. 3, p. 340, doi. 10.1111/pcmr.12469
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Degree of polymerization of 5,6-dihydroxyindolederived eumelanin from chemical degradation study.
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- Pigment Cell & Melanoma Research, 2014, v. 27, n. 4, p. 664, doi. 10.1111/pcmr.12254
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Tuning the photophysical and chiroptical properties of [4]helicene‐diketopyrrolopyrroles.
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- Chirality, 2023, v. 35, n. 11, p. 805, doi. 10.1002/chir.23593
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Rational design of diketopyrrolopyrrole-based multifunctional materials for organic light-emitting diodes and organic solar cells.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2018, v. 137, n. 11, p. 1, doi. 10.1007/s00214-018-2347-4
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Theoretical study on the transport properties of oligothiophene-diketopyrrolopyrrole derivatives: quinoidal versus aromatic.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2014, v. 133, n. 3, p. 1, doi. 10.1007/s00214-014-1453-1
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Theoretical study of chemosensor for fluoride anion and optical properties of the derivatives of diketopyrrolopyrrole.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2012, v. 131, n. 8, p. 1, doi. 10.1007/s00214-012-1260-5
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Studying of Plasma-Polymerized Pyrrole at Variable Gas Flow Rates Via Plasma Jet.
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- Iraqi Journal of Physics, 2021, v. 19, n. 48, p. 44, doi. 10.30723/ijp.v19i48.593
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Influence of heat pump drying on tomato flavor.
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- Drying Technology, 2016, v. 34, n. 14, p. 1709, doi. 10.1080/07373937.2016.1174937
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Pyrrole and Pyrimidine Derivatives as Possible Electron Donors for Colored Charge-Transfer Complexes with a Weakly Electrophilic Energetic Material, FOX-7: A Theoretical Study.
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- Chinese Journal of Explosives & Propellants, 2023, v. 46, n. 5, p. 390, doi. 10.14077/j.issn.1007-7812.202212011
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ReviewInverse coordination. Organic nitrogen heterocycles as coordination centers. A survey of molecular topologies and systematization. Part 1. Five-membered and smaller rings.
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- Journal of Coordination Chemistry, 2019, v. 72, n. 13, p. 2127, doi. 10.1080/00958972.2019.1641702
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Nickel(II) complexes with mono(imino)pyrrole ligands: preparation, structure and ethylene polymerization behavior.
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- Journal of Coordination Chemistry, 2015, v. 68, n. 23, p. 4212, doi. 10.1080/00958972.2015.1103371
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Malonic Acid as A Green and Efficient Catalyst for the Mass-scale Synthesis of Pyrrole Medicinal Drugs.
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- Makara Journal of Science, 2020, v. 24, n. 3, p. 188, doi. 10.7454/mss.v24i3.1203
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Zn(SO<sub>4</sub>)<sub>2</sub>.7H<sub>2</sub>O Catalyzed One-pot and Facile Synthesis of Highly Substituted Dihydro-2-oxopyrroles at Room Temperature.
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- Makara Journal of Science, 2018, v. 22, n. 2, p. 82, doi. 10.7454/mss.v22i2.8792
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Natural Hydroxyapatite: Green Catalyst for the Synthesis of Pyrroles, Inhibitors of Corrosion.
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- Journal of Chemistry, 2021, p. 1, doi. 10.1155/2021/6613243
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Experimentally Validated Novel Factor XIIa Inhibitors Identified by Docking and Quantum Chemical Post‐processing.
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- Molecular Informatics, 2023, v. 42, n. 2, p. 1, doi. 10.1002/minf.202200205
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Key Structural Features of Azanaphthoquinone Annelated Pyrrole Derivative as Anticancer Agents Based on the Rational Drug Design Approaches.
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- Molecular Informatics, 2013, v. 32, n. 5/6, p. 541, doi. 10.1002/minf.201200132
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Visible Light‐Induced [3+2] Annulation Reaction of Alkenes with Vinyl Azides: Direct Synthesis of Functionalized Pyrroles.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 2, p. 151, doi. 10.1002/cjoc.202300498
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