Works matching DE "ACETOPHENONE derivatives"
Results: 70
Rational Design of a Facially Coordinating P,N,N Ligand for Manganese‐Catalysed Enantioselective Hydrogenation of Cyclic Ketones.
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202212479
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Hydrodeoxygenation Using Magnetic Induction: High‐Temperature Heterogeneous Catalysis in Solution.
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- Angewandte Chemie, 2019, v. 131, n. 33, p. 11428, doi. 10.1002/ange.201904366
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Electrochemical Pinacol Coupling of Acetophenone Using Boron‐Doped Diamond Electrode.
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- ChemElectroChem, 2019, v. 6, n. 16, p. 4153, doi. 10.1002/celc.201900202
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Benzonate derivatives of acetophenone as potent α-glucosidase inhibitors: synthesis, structure–activity relationship and mechanism.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 937, doi. 10.1080/14756366.2019.1604519
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Synthesis and evaluation of new thiadiazole derivatives as potential inhibitors of human carbonic anhydrase isozymes (hCA-I and hCA-II).
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 1, p. 32, doi. 10.3109/14756366.2013.873038
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1-(3- Tert -Butylphenyl)-2,2,2-Trifluoroethanone as a Potent Transition-State Analogue Slow-Binding Inhibitor of Human Acetylcholinesterase: Kinetic, MD and QM/MM Studies.
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- Biomolecules (2218-273X), 2020, v. 10, n. 12, p. 1608, doi. 10.3390/biom10121608
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Green asymmetric reduction of acetophenone derivatives: Saccharomyces cerevisiae and aqueous natural deep eutectic solvent.
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- Biotechnology Letters, 2019, v. 41, n. 2, p. 253, doi. 10.1007/s10529-018-2631-3
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Isolation, Characterization and Antiproliferative Activity of Secondary Metabolites from Tanacetum alyssifolium (Bornm.) Grierson.
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- Records of Natural Products, 2021, v. 15, n. 2, p. 122, doi. 10.25135/rnp.201.20.07.1702
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Synthesis of some novel 4-amino-4H-1,2,4-triazole-3-thiol derivatives.
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- Journal of the Iranian Chemical Society, 2024, v. 21, n. 5, p. 1291, doi. 10.1007/s13738-024-02997-w
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Recent advances in the application of acetophenone in heterocyclic compounds synthesis.
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- Journal of the Iranian Chemical Society, 2020, v. 17, n. 2, p. 247, doi. 10.1007/s13738-019-01774-4
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The green synthesis of 2-amino-3-cyanopyridines using SrFe<sub>12</sub>O<sub>19</sub> magnetic nanoparticles as efficient catalyst and their application in complexation with Hg<sup>2+</sup> ions.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 2, p. 365, doi. 10.1007/s13738-018-1514-9
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Two novel coumarins bearing an acetophenone derivative from the leaves of Melicope Quercifolia.
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- Natural Product Research, 2021, v. 35, n. 8, p. 1256, doi. 10.1080/14786419.2019.1644634
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Isolation and identification of new prenylated acetophenone derivatives from Acronychia oligophlebia.
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- Natural Product Research, 2019, v. 33, n. 15, p. 2230, doi. 10.1080/14786419.2018.1490902
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Application of α-bromination reaction on acetophenone derivatives in experimental teaching: a chemical innovation experiment engaging junior undergraduates.
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- BMC Chemistry, 2024, v. 18, p. 1, doi. 10.1186/s13065-024-01145-y
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Synthesis and Characterization of some new heterocyclic derivatives from terphthaldehyde and study of their biological activity.
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- Journals Kufa for Chamical, 2023, v. 3, n. 1, p. 223, doi. 10.36329/jkcm/2023/v3.i1.12260
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SYNTHESIS OF SOME NEW THIAZEPINE COMPOUNDS DERIVED FROM CHALCONES AND EVALUATION THERE BIOCHEMICAL AND BIOLOGICAL ACTIVITY.
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- Biochemical & Cellular Archives, 2019, v. 19, n. 2, p. 4545, doi. 10.35124/bca.2019.19.2.4545
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Synthesis of Pyridine Derivatives from Acetophenone and Ammonium Acetate by Releasing CH<sub>4</sub>.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 8, p. 1332, doi. 10.1002/ajoc.201900323
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Immobilization of Alcohol Dehydrogenases on Silica-Based Supports and Their Application in Enantioselective Ketone Reductions.
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- Catalysts (2073-4344), 2024, v. 14, n. 2, p. 148, doi. 10.3390/catal14020148
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Organometallic Ru(III) Catalysts for α‐Alkylation of Carbonyl Compounds using Alcohols: Mechanistic Insights via Detection of Key Intermediates.
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- Chemistry - An Asian Journal, 2025, v. 20, n. 1, p. 1, doi. 10.1002/asia.202400811
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Porous Protein Crystals as Catalytic Vessels for Organometallic Complexes.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 5, p. 1373, doi. 10.1002/asia.201301347
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Chemoenzymatic Synthesis of Enantiopure Amino Alcohols from Simple Methyl Ketones.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 34, p. 1, doi. 10.1002/ejoc.202201471
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PREPARATION, IDENTIFICATION AND STUDY THE BIOLOGICAL ACTIVITY OF NOVEL HETEROCYCLIC COMPOUNDS DERIVED FROM AZO-CHALCONE.
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- Chemical Problems / Kimya Problemləri, 2025, v. 23, n. 2, p. 272, doi. 10.32737/2221-8688-2025-2-272-285
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SOME ACETOPHENONE DERIVATIVES AS CORROSION INHIBITORS.
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- Chemical Problems / Kimya Problemləri, 2019, v. 17, n. 2, p. 302, doi. 10.32737/2221-8688-2019-2-302-309
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Asymmetric reduction of acetophenone derivatives by Lens culinaris.
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- Biocatalysis & Biotransformation, 2012, v. 30, n. 5/6, p. 469, doi. 10.3109/10242422.2012.743120
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Organocatalytic Synthesis of Lactones by the Oxidation of Alkenoic Acids.
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- ChemCatChem, 2017, v. 9, n. 21, p. 4120, doi. 10.1002/cctc.201700837
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Reactions of ketene aminals with n-arylmaleimides and dimethyl acetylenedicarboxylate, a direct pathway to derivatives of pyrrolo[1,2- a]imidazole and imidazo[1,2- a]pyridine.
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- Chemistry of Heterocyclic Compounds, 2012, v. 48, n. 8, p. 1204, doi. 10.1007/s10593-012-1123-y
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IN VITRO PROSPECTION OF ANTICANCER ACTIVITY OF SOME BROMINATED DERIVATIVES WITH ACETOPHENONE SCAFFOLD.
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- Farmacia, 2024, v. 72, n. 2, p. 418, doi. 10.31925/farmacia.2024.2.19
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A Facile Synthesis of Polycyclic Pyrimidine Fluorophores via Inter- and Intramolecular Cyclization of Activated 2-Amino-3,6-disubstitued Pyrimidin-4-ones.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 1, p. 148, doi. 10.1134/S1070363220010235
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Synthesis and Antimicrobial Activity of (<italic>Z</italic>)-3-{[3-Oxobenzofuran-2(3<italic>H</italic>)-ylidene]methyl}-4<italic>H</italic>-chromen-4-one Derivatives.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 3, p. 566, doi. 10.1134/S1070363218030283
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Natural-derived acetophenones: chemistry and pharmacological activities.
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- Natural Products & Bioprospecting, 2024, v. 14, n. 1, p. 1, doi. 10.1007/s13659-024-00447-x
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Synthesis of Oximes with NH<sub>2</sub>OH.HCl/DOWEX(R)50WX4 System.
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- Journal of the Chinese Chemical Society, 2012, v. 59, n. 9, p. 1119, doi. 10.1002/jccs.201200011
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Hydrosilylation of Ketones Catalyzed by Iron Iminobipyridine Complexes and Accelerated by Lewis Bases.
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- ChemPlusChem, 2019, v. 84, n. 8, p. 1094, doi. 10.1002/cplu.201900366
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The Asymmetric Reduction of Acetophenone and Its Derivatives to ( S)-Aromatic Secondary Alcohols by Rhodotorula mucilaginosa CCTCC M2014255 Resting Cells.
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- Catalysis Letters, 2016, v. 146, n. 6, p. 1079, doi. 10.1007/s10562-016-1730-9
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Ionic‐Liquid‐Catalyzed Synthesis of Imines, Benzimidazoles, Benzothiazoles, Quinoxalines and Quinolines through C−N, C−S, and C−C Bond Formation.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 48, p. 6705, doi. 10.1002/ejoc.202101135
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Natural Products as Sources of New Fungicides (I): Synthesis and Antifungal Activity of Acetophenone Derivatives Against Phytopathogenic Fungi.
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- Chemical Biology & Drug Design, 2013, v. 81, n. 4, p. 545, doi. 10.1111/cbdd.12064
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Replacement of the Methylene of Dihydrochalcones with Oxygen: Synthesis and Biological Evaluation of 2-Phenoxyacetophenones.
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- Chemical Biology & Drug Design, 2012, v. 80, n. 4, p. 591, doi. 10.1111/j.1747-0285.2012.01432.x
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Green and solvent-free procedure for microwave-assisted synthesis of 2,4,6-triarylpyridines catalysed using MgAlO nanocrystals.
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- Journal of Chemical Sciences, 2013, v. 125, n. 5, p. 1063, doi. 10.1007/s12039-013-0477-8
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Insight into the Willgerodt-Kindler Reaction of ω-Haloacetophenone Derivatives: Mechanistic Implication.
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- Organic Chemistry International, 2014, p. 1, doi. 10.1155/2014/486540
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Ruthenium p‐Cymene Iminophosphonamide Complexes: Activation under Basic Conditions and Transfer Hydrogenation Catalysis.
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- European Journal of Inorganic Chemistry, 2018, v. 2018, n. 20/21, p. 2285, doi. 10.1002/ejic.201701344
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Direct Oxidative Cross-Coupling of Toluene Derivatives and N-Acyl-2-aminoacetophenones.
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- Advanced Synthesis & Catalysis, 2017, v. 359, n. 1, p. 39, doi. 10.1002/adsc.201600712
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Comparison between Electropolymers of 3,5-Dihydroxybenzoic Acid and 2′,6′-Dihydroxyacetophenone in Dimethyl Sulfoxide and Their Analytical Performance towards Selected Analytes with the Role of the Washing Liquid.
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- Molecules, 2024, v. 29, n. 16, p. 3972, doi. 10.3390/molecules29163972
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Traveling across Life Sciences with Acetophenone—A Simple Ketone That Has Special Multipurpose Missions.
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- Molecules, 2023, v. 28, n. 1, p. 370, doi. 10.3390/molecules28010370
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UHPLC-MS Metabolome Fingerprinting: The Isolation of Main Compounds and Antioxidant Activity of the Andean Species Tetraglochin ameghinoi (Speg.) Speg.
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- Molecules, 2018, v. 23, n. 4, p. 793, doi. 10.3390/molecules23040793
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Synthesis and DFT Calculations of Novel Vanillin-Chalcones and Their 3-Aryl-5-(4-(2- (dimethylamino)- ethoxy)-3-methoxyphenyl)- 4,5-dihydro-1H-pyrazole-1-carbaldehyde Derivatives as Antifungal Agents.
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- Molecules, 2017, v. 22, n. 9, p. 1476, doi. 10.3390/molecules22091476
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Taguchi analysis and asymmetric keto-reduction of acetophenone and its derivatives by soil filamentous fungal isolate: Penicillium rubens VIT SS1.
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- Preparative Biochemistry & Biotechnology, 2020, v. 50, n. 10, p. 1042, doi. 10.1080/10826068.2020.1786697
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A Green Synthesis of Novel Derivatives of Thiazole-5-One Using Magnetic Supported Copper Nanocatalyst (γ-Fe<sub>2</sub>O<sub>3</sub>@HAp@CPTMS@AT@Cu(ӀI)).
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- Polycyclic Aromatic Compounds, 2023, v. 43, n. 9, p. 8201, doi. 10.1080/10406638.2022.2146147
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Four-Component Heterocyclization Reaction for the One-Pot Synthesis of 2,4-Dichloro-Substituted Pyrano/Furo[2,3-d]pyrimidines in an Environmentally Benign Procedure Mediated by Ceric Ammonium Nitrate in Phosphorus Ionic Liquid.
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- Polycyclic Aromatic Compounds, 2023, v. 43, n. 2, p. 1566, doi. 10.1080/10406638.2022.2030769
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Sesquiterpene Coumarins, Chromones, and Acetophenone Derivatives with Selective Cytotoxicities from the Roots of Ferula caspica M. Bieb. (Apiaceae).
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- Pharmaceuticals (14248247), 2024, v. 17, n. 10, p. 1254, doi. 10.3390/ph17101254
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Monosubstituted Acetophenone Thiosemicarbazones as Potent Inhibitors of Tyrosinase: Synthesis, Inhibitory Studies, and Molecular Docking.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 1, p. 74, doi. 10.3390/ph14010074
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Corrigendum to “Synthesis of Kojic Ester Derivatives as Potential Antibacterial Agent”.
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- Journal of Chemistry, 2019, p. 1, doi. 10.1155/2019/7357830
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