Works matching DE "ACETOPHENONE"
Results: 663
Asymmetric Synthesis of (R)-1-Phenylethanol.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 13, p. 3561, doi. 10.1134/S1070363224130164
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Biodegradation of an Organoselenium Compound to Elemental Selenium by Lentinula edodes (Shiitake) Mushroom.
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- Biological Trace Element Research, 2012, v. 149, n. 1, p. 97, doi. 10.1007/s12011-012-9399-4
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Metabolically driven equilibrium shift of asymmetric animation of ketones by ω-transaminase using alanine as an amino donor.
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- Bioscience, Biotechnology & Biochemistry, 2014, v. 78, n. 10, p. 1788, doi. 10.1080/09168451.2014.930328
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Asymmetric Synthesis of (S)-α-Methylbenzylamine by Recombinant Escherichia coli Co-Expressing Omega-Transaminase and Acetolactate Synthase.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 11, p. 3030, doi. 10.1271/bbb.80410
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Antimelanogenic Activity of 3,4-Dihydroxyacetophenone: Inhibition of Tyrosinase and MITF.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 2, p. 532, doi. 10.1271/bbb.70.532
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Tetra- n-butylammonium Bromide: A Simple but Efficient Organocatalyst for Alcohol Oxidation under Mild Conditions.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 8, p. 1741, doi. 10.1002/adsc.201400100
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Molecular Iodine-Mediated Domino Reaction for the Synthesis of Benzamides, 2,2-Diazidobenzofuran-3(2 H)-ones and Benzoxazolones.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 18, p. 3591, doi. 10.1002/adsc.201300668
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Prelog and anti-Prelog stereoselectivity of two ketoreductases from Candida glabrata.
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- Biotechnology Letters, 2013, v. 35, n. 9, p. 1469, doi. 10.1007/s10529-013-1228-0
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Superabsorbed alcohol dehydrogenase—a new catalyst for asymmetric reductions.
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- Biotechnology Letters, 2009, v. 31, n. 11, p. 1717, doi. 10.1007/s10529-009-0062-x
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New Synthetic Approaches to Naturally Occurring and Unnatural Pyranoflavones.
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- Helvetica Chimica Acta, 2013, v. 96, n. 4, p. 644, doi. 10.1002/hlca.201200278
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Rapid Synthesis of Novel and Known Coumarin-3-carboxylic Acids Using Stannous Chloride Dihydrate under Solvent-Free Conditions.
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- Helvetica Chimica Acta, 2012, v. 95, n. 3, p. 455, doi. 10.1002/hlca.201100342
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A Novel 1-Glycosyl-1 H-triazole-Based P, N Ligand for Rhodium-Catalyzed Asymmetric Hydrosilylation of Ketones.
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- Helvetica Chimica Acta, 2010, v. 93, n. 12, p. 2433, doi. 10.1002/hlca.201000093
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First Authentication of Kostanecki's Triketone and Multimolecular Reaction of Aromatic Aldehydes with Acetophenone.
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- Helvetica Chimica Acta, 2009, v. 92, n. 6, p. 1102, doi. 10.1002/hlca.200800413
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Secondary metabolites from the aerial parts of Verbascum dudleyanum and their biological activities.
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- Chemistry of Natural Compounds, 2008, v. 44, n. 3, p. 292, doi. 10.1007/s10600-008-9045-8
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One-pot synthesis of [4-(tert-butyl)-1H-pyrrol-3-yl](phenyl)methanone from tosylmethyl isocyanide and carbonyl compound.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 7, p. 700, doi. 10.1007/s10593-018-2335-6
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Synthesis of 5-(pyrazol-1-yl)-1,2,3-thiadiazoles.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 2, p. 236, doi. 10.1007/s10593-017-2045-5
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Synthesis of 1,2,3-Triazolo[1,5- а]Pyridin-8-Ium-3-Olates.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 2, p. 199, doi. 10.1007/s10593-015-1681-x
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Synthesis of 4-Acyl-3-Aminofurazans from 3,4-Diacylfuroxans.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 8, p. 1154, doi. 10.1007/s10593-014-1576-2
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Synthesis of 2,5-Dihydroisothiazole Derivatives. 2*. 3-Aryl(Hetaryl)-Substituted 2-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 1, p. 87, doi. 10.1007/s10593-014-1451-1
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Antimicrobial, antioxidant and cytotoxic evaluation of diazenyl chalcones along with insights to mechanism of interaction by molecular docking studies.
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- BMC Chemistry, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13065-019-0596-5
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Isolation and characterization of a novel Rhodococcus strain with switchable carbonyl reductase and para-acetylphenol hydroxylase activities.
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- Journal of Industrial Microbiology & Biotechnology, 2013, v. 40, n. 1, p. 11, doi. 10.1007/s10295-012-1199-5
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Production of chiral alcohols from prochiral ketones by microalgal photo-biocatalytic asymmetric reduction reaction.
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- Journal of Industrial Microbiology & Biotechnology, 2012, v. 39, n. 6, p. 835, doi. 10.1007/s10295-012-1088-y
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Didymosphaeria igniaria: a new microorganism useful for the enantioselective reduction of aryl-aliphatic ketones.
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- Journal of Industrial Microbiology & Biotechnology, 2010, v. 37, n. 11, p. 1121, doi. 10.1007/s10295-010-0759-9
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Preparation of Bimetallic CuZn@mSiO<sub>2</sub> Yolk‐Shell Catalyst for the Selective Oxidation of Cumene to Acetophenone.
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- ChemNanoMat, 2022, v. 8, n. 3, p. 1, doi. 10.1002/cnma.202100509
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Thermodynamic properties of P-methyl acetophenone with cyclohexylamine, cyclohexanol, and cyclohexane at various temperatures (strong and weak interactions).
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- Physics & Chemistry of Liquids, 2024, v. 62, n. 4, p. 356, doi. 10.1080/00319104.2024.2306606
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Studies on solution properties of ternary mixture of acetophenone + n -amyl alcohol + dichloromethane and its corresponding binaries at 298.15 K.
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- Physics & Chemistry of Liquids, 2014, v. 52, n. 1, p. 100, doi. 10.1080/00319104.2011.604779
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Synthesis of 4-(2-substituted hydrazinyl)benzenesulfonamides and their carbonic anhydrase inhibitory effects.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 4, p. 568, doi. 10.3109/14756366.2015.1047359
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Synthesis and Biologically Activity of Novel 2-Chloro-3-Formyl - 1,5-Naphthyridine Chalcone Derivatives.
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- Journal of Chemical Health Risks, 2022, v. 12, n. 1, p. 73, doi. 10.22034/jchr.2022.688560
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3-Trifluoroacetamidobenzoyltrifluoroacetone and its europium complexes.
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- Doklady Chemistry, 2011, v. 439, n. 1, p. 209, doi. 10.1134/S0012500811070111
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Synthesis of p-Chlorocelecoxib from 4-Methylacetophenone & its Spectral Characterization.
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- Indo Global Journal of Pharmaceutical Sciences, 2012, v. 2, n. 3, p. 239, doi. 10.35652/igjps.2012.29
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Blockade of Eosinophil-Induced Bronchial Epithelial-Mesenchymal Transition with a Geranyl Acetophenone in a Coculture Model.
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- Frontiers in Pharmacology, 2017, p. 1, doi. 10.3389/fphar.2017.00837
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Visible Light-Driven CO<sub>2</sub> Insertion on Phenylacetylene to Phenylpropiolic Acid Using Soft-Oxometalates.
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- Journal of Molecular & Engineering Materials, 2021, v. 9, n. 4, p. 1, doi. 10.1142/S2251237321400049
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Synthesis, characterization, and evaluation of differently sulfonated resins as novel carriers for drug delivery.
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- Designed Monomers & Polymers, 2013, v. 16, n. 1, p. 56, doi. 10.1080/15685551.2012.705490
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Facile synthesis of environmental friendly halogen-free microporous terpolymer from renewable source with enhanced physical properties.
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- Designed Monomers & Polymers, 2012, v. 15, n. 6, p. 587, doi. 10.1080/15685551.2012.705501
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- Article
Polyimide-Supported Dichloro-1,3-bis(p-dimethylaminobenzyl)benzimidazolidin-2-ilidenruthenium (II) as Effective Catalyst for Hydrosilylation Reactions.
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- Designed Monomers & Polymers, 2008, v. 11, n. 5, p. 409, doi. 10.1163/156855508X328112
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A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39375-8
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Evaluation of the migration of 15 photo-initiators from cardboard packaging into Tenax using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).
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- Food Additives & Contaminants. Part A: Chemistry, Analysis, Control, Exposure & Risk Assessment, 2014, v. 31, n. 4, p. 767, doi. 10.1080/19440049.2014.886340
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- Article
Microwave-Assisted Synthesis, Characterization, Docking Studies and Molecular Dynamic of Some Novel Phenyl Thiazole Analogs as Xanthine Oxidase Inhibitor.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 9, p. 3919, doi. 10.1007/s13738-022-02574-z
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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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An efficient, green solvent-free protocol for the synthesis of 2,4,6-triarylpyridines using reusable heterogeneous activated Fuller’s earth catalyst.
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- Journal of the Iranian Chemical Society, 2018, v. 15, n. 11, p. 2455, doi. 10.1007/s13738-018-1434-8
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Nano-silica sulfuric acid catalyzed the efficient synthesis of 1,3,5-triarylbenzenes under microwave irradiation.
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- Journal of the Iranian Chemical Society, 2012, v. 9, n. 5, p. 791, doi. 10.1007/s13738-012-0089-0
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Intermolecular Photoredox Coupling: Alternative to Norrish Type II Reaction and Yang Cyclization in Ketones with γ‐C−H Bonds.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 26, p. 3665, doi. 10.1002/ejoc.202100434
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Iodine‐Mediated Condensation–Cyclization of α‐Azido Ketones with p‐Toluenesulfonyl Hydrazide for Synthesis of 4‐Aryl‐NH‐1,2,3‐Triazoles.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 15, p. 2233, doi. 10.1002/ejoc.202000146
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Valorization of Methyl Azelaaldehydate – A Vegetable Oil Based Platform Molecule for the Synthesis of Monomers through Stetter Reaction.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 6, p. 1251, doi. 10.1002/ejoc.201801611
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Metal‐Free Synthesis of Furocoumarins: An Approach via Iodine‐Promoted One‐Pot Cyclization between 4‐Hydroxycoumarins and Acetophenones.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 32, p. 4431, doi. 10.1002/ejoc.201800983
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One‐Pot Sequential Bromination and Fluorination to Access 3‐Fluoroimidazo[1,2‐a]pyridines from Arylketones.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 26, p. 3432, doi. 10.1002/ejoc.201800578
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Direct Acetophenone–Acetophenone Crossed Aldol Reaction and Aldol Self‐Reaction Promoted by a Tethered Ru–S Complex.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 19, p. 2290, doi. 10.1002/ejoc.201800132
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Solvent and Base in One: Tetra- n-butylammonium Acetate as a Multi-Purpose Ionic Liquid Medium for Ru-Catalyzed Directed Mono- and Di- o-C-H Arylation Reactions.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 42, p. 6274, doi. 10.1002/ejoc.201701022
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Enantioselective Synthesis of 2,3-Dihydrofurans via Ammonium Ylides.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 40, p. 6077, doi. 10.1002/ejoc.201701176
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Modular De novo Synthesis of Unsymmetrical BODIPY Dyes Possessing Four Different Aryl Substituents.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 31, p. 4580, doi. 10.1002/ejoc.201700773
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