Works matching DE "TETRALONES"
Results: 49
Tandem aldol condensation-Diels-Alder-aromatization sequence of reactions: a new pathway for the synthesis of 2-tetralone derivatives.
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- Canadian Journal of Chemistry, 2016, v. 94, n. 9, p. 733, doi. 10.1139/cjc-2016-0246
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Enantioseparation of nine indanone and tetralone derivatives by HPLC using carboxymethyl-β-cyclodextrin as the mobile phase additive.
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- Chirality, 2017, v. 29, n. 1, p. 38, doi. 10.1002/chir.22665
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Enantioselective Dynamic Process Reduction of α- and β-Tetralone and Stereoinversion of Resulting Alcohols in a Selected Strain Culture.
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- Current Microbiology, 2012, v. 65, n. 2, p. 189, doi. 10.1007/s00284-012-0143-2
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Efficient synthesis of novel imidazo[1,2-a]pyrimidine derivatives via one-pot three-component procedure.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 6, p. 1049, doi. 10.1007/s13738-014-0564-x
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Quantitative Determination of Bioactive 4-Hydroxy-α-Tetralone, Tetralone-4-O-β-D-Glucopyranoside and Ellagic Acid in Ammannia baccifera (Linn.) by Reversed-Phase High-Performance Liquid Chromatography.
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- Journal of Chromatographic Science, 2013, v. 51, n. 1, p. 21, doi. 10.1093/chromsci/bms099
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Antimicrobial and cytotoxic juglones from the immature exocarps of Juglans mandshurica.
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- Natural Product Research, 2019, v. 33, n. 22, p. 3203, doi. 10.1080/14786419.2018.1468326
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Iodine‐Promoted Synthesis of 2‐Naphthyl Thioethers from Tetralones and Sulfonyl Hydrazides.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 2, p. 234, doi. 10.1002/ajoc.201800662
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Ru<sup>II</sup>-Catalyzed ortho-Sulfonamidation of α-Tetralones with Sulfonyl Azides and Synthesis of Sivelestat by Aromatic C−H Activation.
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- Asian Journal of Organic Chemistry, 2017, v. 6, n. 12, p. 1851, doi. 10.1002/ajoc.201700356
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Structural studies of (E)-2-(benzylidene)-1- tetralone derivatives: crystal structures and Hirshfeld surface analysis.
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- Zeitschrift für Kristallographie. Crystalline Materials, 2017, v. 232, n. 10, p. 697, doi. 10.1515/zkri-2017-2048
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Tuning O<sub>2</sub> Reactivity through Synergistic Photo/Copper Catalysis: Direct Synthesis of 4-Aryl tetralones via Cyclodimerization-Oxygenation of Styrenes.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 15, p. 2117, doi. 10.1002/asia.201600758
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Enantioselective bioreduction of cyclic alkanones by whole cells of Candida Species.
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- Biocatalysis & Biotransformation, 2013, v. 31, n. 3, p. 123, doi. 10.3109/10242422.2013.778252
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Ketoreductase activity for reduction of substituted-β-tetralones utilizing aqueous-organic systems and β-cyclodextrin derivatives.
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- Biocatalysis & Biotransformation, 2012, v. 30, n. 2, p. 226, doi. 10.3109/10242422.2012.662960
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Asymmetric Reduction of Substituted 2-Tetralones by Thermoanaerobacter pseudoethanolicus Secondary Alcohol Dehydrogenase.
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- ChemCatChem, 2017, v. 9, n. 8, p. 1487, doi. 10.1002/cctc.201601618
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Steric and Electronic Manipulation of the Anagostic Interaction in 1-Tetralone Oxime and Imine Complexes of Rhodium(I).
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- European Journal of Inorganic Chemistry, 2016, v. 2016, n. 1, p. 64, doi. 10.1002/ejic.201501122
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Efficient ionic liquid-catalysed synthesis and antimicrobial studies of 4,6-diaryl- and 4,5-fused pyrimidine-2-thiones.
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- Journal of Chemical Research, 2012, v. 36, n. 12, p. 718, doi. 10.3184/174751912X13523931169712
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Reaction of α-tetralone, 1 H-tetrazol-5-amine, and aromatic aldehydes upon microwave irradiation - a convenient method for the synthesis of 5,6,7,12-tetrahydrobenzo[ h]tetrazolo[5,1- b]quinazolines.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 11, p. 918, doi. 10.1007/s10593-017-1985-0
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- Article
A Validated LC Method for Separation and Determination of Tetralone-4-O-β-D-Glucopyranoside and 4-Hydroxy-α-Tetralone in Ammannia multiflora.
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- Chromatography Research International, 2012, p. 1, doi. 10.1155/2012/162302
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- Article
Regioselective Electrochemical Cyclobutanol Ring Expansion to 1‐Tetralones.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 5, p. 854, doi. 10.1002/ejoc.202001535
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Bioactive Spirobisnaphthalenes and Lactones from a Cup Fungus Plectania sp. Collected in the Tibet Plateau Region.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 25, p. 4338, doi. 10.1002/ejoc.201600562
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Crystal structure of ( E)-2-(4-hydroxy-3-methoxybenzylidene)-6-methoxy-3,4-dihydronaphthalen-1(2 H)-one, C<sub>19</sub>H<sub>18</sub>O<sub>4</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2017, v. 232, n. 2, p. 203, doi. 10.1515/ncrs-2016-0195
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Evaluation of 2-benzylidene-1-tetralone derivatives as antagonists of A<sub>1</sub> and A<sub>2A</sub> adenosine receptors.
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- Chemical Biology & Drug Design, 2018, v. 91, n. 1, p. 234, doi. 10.1111/cbdd.13074
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The Synthesis and Evaluation of C7-Substituted α-Tetralone Derivatives as Inhibitors of Monoamine Oxidase.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 895, doi. 10.1111/cbdd.12508
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- Article
4-Hydroxy- α-Tetralone and its Derivative as Drug Resistance Reversal Agents in Multi Drug Resistant E scherichia coli.
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- Chemical Biology & Drug Design, 2014, v. 83, n. 4, p. 482, doi. 10.1111/cbdd.12263
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- Article
Juglans mandshurica Maxim.: A Review of Its Traditional Usages, Phytochemical Constituents, and Pharmacological Properties.
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- Frontiers in Pharmacology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphar.2020.569800
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Synthesis of [60]Fullerene-Fused Tetralones via Palladium- Catalyzed Ketone-Directed sp<sup>2</sup> CH Activation and sp<sup>3</sup> CH Functionalization.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 10, p. 1548, doi. 10.1002/adsc.201501112
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Ene Reductase Enzymes for the Aromatisation of Tetralones and Cyclohexenones to Naphthols and Phenols.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 5, p. 731, doi. 10.1002/adsc.201500818
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N,N′-Dioxide-Magnesium Ditriflate Complex-Catalyzed Asymmetric α-Hydroxylation of β-Keto Esters and β-Keto Amides.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 10, p. 1924, doi. 10.1002/adsc.201300335
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Evaluation of Silica-H<sub>2</sub>SO<sub>4</sub> as an Efficient Heterogeneous Catalyst for the Synthesis of Chalcones.
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- Molecules, 2013, v. 18, n. 8, p. 10081, doi. 10.3390/molecules180810081
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Acid-Catalyzed Synthesis of Thiazolidin-4-ones.
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- Polycyclic Aromatic Compounds, 2018, v. 38, n. 4, p. 311, doi. 10.1080/10406638.2016.1207685
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L-proline catalyzed an efficient multicomponent one-pot synthesis of poly substituted pyridines.
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- Organic Communications, 2012, v. 5, n. 4, p. 186
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Highly Antiplasmodial Non-Natural Oxidative Products of Dioncophylline A: Synthesis, Absolute Configuration, and Conformational Stability.
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- Chemistry - A European Journal, 2015, v. 21, n. 41, p. 14507, doi. 10.1002/chem.201501657
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Asymmetric α-Hydroxylation of Tetralone-Derived β-Ketoesters by Using a Guanidine-Urea Bifunctional Organocatalyst in the Presence of Cumene Hydroperoxide.
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- Chemistry - A European Journal, 2013, v. 19, n. 49, p. 16740, doi. 10.1002/chem.201303006
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Total Synthesis of Rishirilide B by Organocatalytic Oxidative Kinetic Resolution: Revision of Absolute Configuration of (+)-Rishirilide B.
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- Angewandte Chemie, 2017, v. 129, n. 23, p. 6709, doi. 10.1002/ange.201701431
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Bifunctional Brønsted Base Catalyst Enables Regio-, Diastereo-, and Enantioselective C<sub>α</sub>-Alkylation of β-Tetralones and Related Aromatic-Ring-Fused Cycloalkanones.
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- Angewandte Chemie, 2017, v. 129, n. 8, p. 2091, doi. 10.1002/ange.201612332
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- Article
A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins.
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- Angewandte Chemie, 2014, v. 126, n. 52, p. 14656, doi. 10.1002/ange.201408929
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- Article
Stereocontrolled Syntheses of Tetralone- and Naphthyl-Type Lignans by a One-Pot Oxidative [3,3] Rearrangement/Friedel-Crafts Arylation.
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- Angewandte Chemie, 2014, v. 126, n. 5, p. 1419, doi. 10.1002/ange.201307659
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Enantioselective Organocatalytic Fluorination-Induced Wagner-Meerwein Rearrangement.
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- Angewandte Chemie, 2013, v. 125, n. 35, p. 9436, doi. 10.1002/ange.201303527
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Juglanones A and B: Two Novel Tetralone Dimers from Walnut Pericarp ( Juglans regia).
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- Helvetica Chimica Acta, 2013, v. 96, n. 6, p. 1031, doi. 10.1002/hlca.201200525
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High pressure assisted synthetic approach for novel 6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine and 5,6-dihydrobenzo[h]quinoline derivatives and their assessment as anticancer agents.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-78590-x
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Tetralone Derivatives From a Deep-Sea-Derived Fungus Cladosporium Sp. HDN17-58.
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- Natural Product Communications, 2021, v. 16, n. 4, p. 1, doi. 10.1177/1934578X211008322
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Chemical Constituents of the Gorgonian-Derived Fungus Chaetomium globosum.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 1, p. 199, doi. 10.1007/s10600-017-1950-2
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Physicochemical Characterization of a Thermostable Alcohol Dehydrogenase from <i>Pyrobaculum aerophilum</i>.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0063828
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Synthesis of 5-Carbapterocarpens by α-Arylation of Tetralones Followed by One-Pot Demethylation/Cyclization with BBr<sub>3</sub>.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 6, p. 1314, doi. 10.1002/ejoc.201301505
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- Article
Asymmetric Organocatalytic Protonation of Silyl Enolates Catalyzed by Simple and Original Betaines Derived from Cinchona Alkaloids.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 34, p. 7693, doi. 10.1002/ejoc.201301345
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Heterogeneous Palladium-Catalyzed Synthesis of Aromatic Ethers by Solvent-Free Dehydrogenative Aromatization: Mechanism, Scope, and Limitations Under Aerobic and Non-Aerobic Conditions.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 26, p. 5902, doi. 10.1002/ejoc.201300485
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Bifunctional Brønsted Base Catalyst Enables Regio-, Diastereo-, and Enantioselective C<sub>α</sub>-Alkylation of β-Tetralones and Related Aromatic-Ring-Fused Cycloalkanones.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 8, p. 2059, doi. 10.1002/anie.201612332
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- Article
α-Arylation and Ring Expansion of Annulated Cyclobutanones: Stereoselective Synthesis of Functionalized Tetralones.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 3, p. 748, doi. 10.1002/anie.201608449
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Stereocontrolled Syntheses of Tetralone- and Naphthyl-Type Lignans by a One-Pot Oxidative [3,3] Rearrangement/Friedel-Crafts Arylation.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 5, p. 1395, doi. 10.1002/anie.201307659
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- Article
One Pot.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 1, p. 294, doi. 10.1002/jhet.2284
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