Works matching DE "ARYL esters"
Results: 110
Anti-aging and anti-microbial effects of melleolide on various types of yeast.
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- Bioscience, Biotechnology & Biochemistry, 2014, v. 78, n. 3, p. 455, doi. 10.1080/09168451.2014.885826
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Synthesis of 10-Aryl- and 10-(Arylmethyl)acridin-9(10 H)-ones via the Reaction of (2-Fluorophenyl)(2-halophenyl)methanones with Benzenamines and Arylmethanamines.
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- Helvetica Chimica Acta, 2013, v. 96, n. 3, p. 389, doi. 10.1002/hlca.201200343
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Arene C–H borylation strategy enabled by a non-classical boron cluster-based electrophile.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37258-6
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Synthesis and biological activities of 1H-indole-1-carboxylic acid aryl esters as a marine antifouling coating.
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- Journal of Coatings Technology & Research, 2020, v. 17, n. 2, p. 553, doi. 10.1007/s11998-019-00305-3
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Competent synthesis of biaryl analogs via asymmetric Suzuki–Miyaura cross-coupling for the development of anti-inflammatory and analgesic agents.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 6, p. 2421, doi. 10.1007/s13738-021-02460-0
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Secondary metabolites of six Siberian and Crimean Armillaria species and their in vitro phytotoxicity to pine, larch and poplar.
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- iForest - Biogeosciences & Forestry, 2022, v. 15, n. 1, p. 38, doi. 10.3832/ifor3840-014
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Synthesis of Indoles by Reductive Cyclization of Nitro Compounds Using Formate Esters as CO Surrogates.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 34, p. 4876, doi. 10.1002/ejoc.202100789
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Cu‐Mediated Radiofluorination of Aryl Pinacolboronate Esters: Alcohols as Solvents with Application to 6‐L‐[<sup>18</sup>F]FDOPA Synthesis.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 45, p. 7079, doi. 10.1002/ejoc.202001198
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Palladium‐Catalyzed Decarboxylative Generation and Propargylation of 2‐Azaallyl Anions.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 24, p. 3964, doi. 10.1002/ejoc.201900537
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Pd‐Catalyzed Decarboxylative Asymmetric Protonation (DAP) Using Chiral PHOX Ligands vs. Chiral Ligand‐Free Conditions Employing (1R,2S)(–)‐Ephedrine – A Comparison Study.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 13, p. 2421, doi. 10.1002/ejoc.201900267
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- Article
Visible-Light-Induced Meerwein Cascade Reactions for the Preparation of α-Aryl Esters.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 26, p. 5775, doi. 10.1002/ejoc.201500659
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Nickel-Catalyzed Decarbonylative Coupling of Aryl Esters and Arylboronic Acids.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 25, p. 5546, doi. 10.1002/ejoc.201500630
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Ni-Catalyzed Stannylation of Aryl Esters via C−O Bond Cleavage.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 12, p. 3187, doi. 10.1002/anie.201611720
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Synthesis of meta-Terphenyl-2,2′′-diols by Anodic C−C Cross-Coupling Reactions.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 36, p. 10872, doi. 10.1002/anie.201605865
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Nickel-Catalyzed Enantioselective CC Bond Formation through C.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 13, p. 4075, doi. 10.1002/anie.201412051
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- Article
Synthesis of Quinoline-2-Carboxylic Acid Aryl Ester and Its Apoptotic Action on PC3 Prostate Cancer Cell Line.
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- Applied Biochemistry & Biotechnology, 2023, v. 195, n. 8, p. 4818, doi. 10.1007/s12010-022-04258-z
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Synthesis and Anticonvulsant Activity of Some Cyclohexanone Derivatives – Knoevenagel Condensation Products.
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- Pharmaceutical Chemistry Journal, 2020, v. 54, n. 9, p. 897, doi. 10.1007/s11094-020-02305-9
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Synthesis and Biological Activity of Quinoline-2-Carboxylic Acid Aryl Esters and Amides.
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- Pharmaceutical Chemistry Journal, 2017, v. 51, n. 5, p. 351, doi. 10.1007/s11094-017-1613-4
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- Article
Machine Learning Models for Predicting Bioavailability of Traditional and Emerging Aromatic Contaminants in Plant Roots.
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- Toxics, 2024, v. 12, n. 10, p. 737, doi. 10.3390/toxics12100737
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- Article
Environmentally Relevant Concentrations of Triphenyl Phosphate (TPhP) Impact Development in Zebrafish.
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- Toxics, 2024, v. 12, n. 5, p. 368, doi. 10.3390/toxics12050368
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Insights into P-Glycoprotein Inhibitors: New Inducers of Immunogenic Cell Death.
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- Cells (2073-4409), 2020, v. 9, n. 4, p. 1033, doi. 10.3390/cells9041033
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- Article
An Amino-Chain Modified β-cyclodextrin: A Supramolecular Ligand for Pd(OAc)2 Acceleration in Suzuki–Miyaura Coupling Reactions in Water.
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- Catalysts (2073-4344), 2019, v. 9, n. 2, p. 111, doi. 10.3390/catal9020111
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The conversion of aryl and heteroaryl methylketones to the corresponding secondary or tertiary amides.
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- Journal of Chemical Research, 2011, v. 35, n. 5, p. 298, doi. 10.3184/174751911X13053065216840
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- Article
Biosynthesis of Protoilludene Sesquiterpene Aryl Esters by Siberian Strains of the Genus Armillaria Fungi.
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- Applied Biochemistry & Microbiology, 2019, v. 55, n. 3, p. 277, doi. 10.1134/S0003683819030153
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- Article
Anti‐inflammatory and anti‐aggregating effects of rangpur in the first trimester of growth: ultra‐performance liquid chromatography–electrospray mass spectrometry profile and quantification of hesperidin.
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- Journal of the Science of Food & Agriculture, 2022, v. 102, n. 10, p. 4151, doi. 10.1002/jsfa.11764
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- Article
Syntheses of some hydrazones derived from 2-(aryloyloxy) benzaldehydes and 2,4-dinitrophenylhydrazine and evaluation of their anticholinesterase and antioxidant activities.
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- Organic Communications, 2022, v. 15, n. 4, p. 324, doi. 10.25135/acg.oc.137.2209.2570
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- Article
Enantioselective synthesis of (R)-tolterodine using lithiation/borylation–protodeboronation methodology.
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- Canadian Journal of Chemistry, 2012, v. 90, n. 11, p. 965, doi. 10.1139/v2012-069
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How Much Does the Hybridization of a Carbon Atom Affect the Transmission of the Substituent Effect on the Chemical Shift?
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 1, p. 295, doi. 10.1002/bkcs.10067
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Silver/manganese dioxide nanorod catalyzed hydrogen-borrowing reactions and tert -butyl ester synthesis.
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- Journal of Chemical Research, 2021, v. 45, p. 708, doi. 10.1177/1747519821989963
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A practical chlorination of tert -butyl esters with PCl<sub>3</sub> generating acid chlorides.
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- Journal of Chemical Research, 2020, v. 44, n. 5/6, p. 301, doi. 10.1177/1747519819898142
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- Article
Exploring the Scope of Tandem Palladium and Isothiourea Relay Catalysis for the Synthesis of α-Amino Acid Derivatives.
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- Molecules, 2020, v. 25, n. 10, p. 2463, doi. 10.3390/molecules25102463
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- Article
Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Aryl Chlorobenzoates with Alkyl Grignard Reagents.
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- Molecules, 2020, v. 25, n. 1, p. 230, doi. 10.3390/molecules25010230
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Pd-Catalyzed Suzuki-Miyaura Cross-Coupling of Pentafluorophenyl Esters.
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- Molecules, 2018, v. 23, n. 12, p. 3134, doi. 10.3390/molecules23123134
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- Article
Three New Sesquiterpene Aryl Esters from the Mycelium of Armillaria mellea.
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- Molecules, 2015, v. 20, n. 6, p. 9994, doi. 10.3390/molecules20069994
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- Article
Overcoming the low reactivity of biobased, secondary diols in polyester synthesis.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34840-2
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- Article
A Facile Preparation of α-Aryl Carboxylic Acid via One-Flow Arndt–Eistert Synthesis.
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- Australian Journal of Chemistry, 2015, v. 68, n. 11, p. 1657, doi. 10.1071/CH15342
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- Article
Liquid crystalline hyperbranched polyesters with phosphorus functional groups.
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- High Performance Polymers, 2021, v. 33, n. 4, p. 383, doi. 10.1177/0954008320960532
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- Article
Rhodium‐Catalyzed ON‐OFF Switchable Hydrogenation Using a Molecular Shuttle Based on a [2]Rotaxane with a Phosphine Ligand.
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- Angewandte Chemie, 2022, v. 134, n. 15, p. 1, doi. 10.1002/ange.202200638
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- Article
Synthesis of Functionalized Silsesquioxane Nanomaterials by Rhodium‐Catalyzed Carbene Insertion into Si−H Bonds.
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- Angewandte Chemie, 2022, v. 134, n. 1, p. 1, doi. 10.1002/ange.202110417
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- Article
Chiral Benzothiophene Synthesis via Enantiospecific Coupling of Benzothiophene S‐Oxides with Boronic Esters.
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- Angewandte Chemie, 2021, v. 133, n. 48, p. 25517, doi. 10.1002/ange.202112180
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- Article
Activation of Aryl Carboxylic Acids by Diboron Reagents towards Nickel‐Catalyzed Direct Decarbonylative Borylation.
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- Angewandte Chemie, 2021, v. 133, n. 46, p. 24715, doi. 10.1002/ange.202106356
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Chiral Arylated Amines via C−N Coupling of Chiral Amines with Aryl Bromides Promoted by Light.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21706, doi. 10.1002/ange.202108587
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Radical 1,4‐Aryl Migration Enabled Remote Cross‐Electrophile Coupling of α‐Amino‐β‐Bromo Acid Esters with Aryl Bromides.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21530, doi. 10.1002/ange.202106273
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Atropo‐Enantioselective Oxidation‐Enabled Iridium(III)‐Catalyzed C−H Arylations with Aryl Boronic Esters.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18680, doi. 10.1002/ange.202106403
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Supercharging Prions via Amyloid‐Selective Lysine Acetylation.
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- Angewandte Chemie, 2021, v. 133, n. 27, p. 15196, doi. 10.1002/ange.202103548
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Nickel/Photoredox‐Catalyzed Asymmetric Reductive Cross‐Coupling of Racemic α‐Chloro Esters with Aryl Iodides.
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- Angewandte Chemie, 2020, v. 132, n. 13, p. 5210, doi. 10.1002/ange.201914175
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- Article
Rational Design of an Iron‐Based Catalyst for Suzuki–Miyaura Cross‐Couplings Involving Heteroaromatic Boronic Esters and Tertiary Alkyl Electrophiles.
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- Angewandte Chemie, 2020, v. 132, n. 13, p. 5430, doi. 10.1002/ange.201914315
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- Article
Base‐free Enantioselective C(1)‐Ammonium Enolate Catalysis Exploiting Aryloxides: A Synthetic and Mechanistic Study.
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- Angewandte Chemie, 2019, v. 131, n. 42, p. 15255, doi. 10.1002/ange.201908627
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Remote Central‐to‐Axial Chirality Conversion: Direct Atroposelective Ester to Biaryl Transformation.
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- Angewandte Chemie, 2018, v. 130, n. 24, p. 7254, doi. 10.1002/ange.201803472
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- Article
Oviposition and flight orientation response of Aedes aegypti to certain aromatic aryl hydrazono esters.
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- Parasitology Research, 2012, v. 111, n. 3, p. 975, doi. 10.1007/s00436-012-2921-y
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