Works matching DE "BUTENOLIDES"
Results: 109
Gold(I)‐Catalyzed Ring‐Closing Alkyne‐Carbonyl Metathesis for the Synthesis of Butenolides.
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- Chemistry - A European Journal, 2023, v. 29, n. 65, p. 1, doi. 10.1002/chem.202302044
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Palladium‐Catalyzed Enantioselective γ‐Arylation of β,γ‐Unsaturated Butenolides.
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- Angewandte Chemie, 2022, v. 134, n. 23, p. 1, doi. 10.1002/ange.202202046
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Biosynthesis of Pseudomonas‐Derived Butenolides.
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- Angewandte Chemie, 2020, v. 132, n. 14, p. 5656, doi. 10.1002/ange.201914154
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Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem‐Hydrogenation or through Carbophilic Activation of Alkynes.
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- Angewandte Chemie, 2019, v. 131, n. 51, p. 18647, doi. 10.1002/ange.201912161
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Inverse‐Electron‐Demand Palladium‐Catalyzed Asymmetric [4+2] Cycloadditions Enabled by Chiral P,S‐Ligand and Hydrogen Bonding.
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- Angewandte Chemie, 2019, v. 131, n. 32, p. 11129, doi. 10.1002/ange.201905993
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Vitamin C and E supplementation alters protein signalling after a strength training session, but not muscle growth during 10 weeks of training.
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- Journal of Physiology, 2014, v. 592, n. 24, p. 5391, doi. 10.1113/jphysiol.2014.279950
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Dietary vitamin C mitigates monocrotophos toxicity in the freshwater fish Clarias batrachus.
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- Aquaculture Nutrition, 2014, v. 20, n. 6, p. 609, doi. 10.1111/anu.12112
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Erratum.
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- Journal of Pesticide Science, 2020, v. 45, n. 4, p. 253, doi. 10.1584/jpestics.C20-01
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Synthesis of butenolides by reactions of 3‐alkenoic acids with diphenyl sulfoxide/oxalyl chloride.
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- Flavour & Fragrance Journal, 2018, v. 33, n. 6, p. 397, doi. 10.1002/ffj.3464
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Chemoselective access to substituted butenolides via a radical cyclization pathway: mechanistic study, limits and application.
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- Pure & Applied Chemistry, 2016, v. 88, n. 3, p. 215, doi. 10.1515/pac-2015-1203
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Strigolactones as Regulators of Symbiotrophy of Plants and Microorganisms.
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- Russian Journal of Plant Physiology, 2018, v. 65, n. 2, p. 151, doi. 10.1134/S1021443718020073
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Molecular aspects of the antagonistic interaction of smoke-derived butenolides on the germination process of Grand Rapids lettuce ( Lactuca sativa) achenes.
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- New Phytologist, 2012, v. 196, n. 4, p. 1060, doi. 10.1111/j.1469-8137.2012.04358.x
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Evidence that KARRIKININSENSITIVE2 (KAI2) Receptors may Perceive an Unknown Signal that is not Karrikin or Strigolactone.
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- Frontiers in Plant Science, 2016, v. 6, p. 1, doi. 10.3389/fpls.2015.01219
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Antiepileptogenic and Neuroprotective Effects of Pergularia daemia on Pilocarpine Model of Epilepsy.
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- Frontiers in Pharmacology, 2017, p. 1, doi. 10.3389/fphar.2017.00440
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Amide‐Based Morita–Baylis–Hillman Carbonates for Phosphine‐Catalyzed Asymmetric (4+2) Annulation<sup>†</sup>.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 24, p. 3269, doi. 10.1002/cjoc.202400657
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Xylazine-Ketamine Anesthesia Following Premedication of New Zealand White Rabbits with Vitamin C.
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- Kafkas Universitesi Veteriner Fakultesi Dergisi, 2016, v. 22, n. 1, p. 115, doi. 10.9775/kvfd.2015.13998
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Ulubelenolide: A New triterpene lactone from Tanacetum chiliophyllum (Fisch. & Mey.) var. monocephalum Grierson.
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- Records of Natural Products, 2015, v. 9, n. 3, p. 419
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Promising Cytotoxic butenolides from the Soybean endophytic fungus Aspergillus terreus: a combined molecular docking and in-vitro studies.
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- Journal of Applied Microbiology, 2023, v. 134, n. 7, p. 1, doi. 10.1093/jambio/lxad129
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A glyoxylate-containing benzene derivative and butenolides from a marine algicolous fungus Aspergillus sp. SCSIO 41304.
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- Natural Product Research, 2023, v. 37, n. 3, p. 441, doi. 10.1080/14786419.2021.1978994
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Octyl substituted butenolides from marine-derived Streptomyces koyangensis.
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- Natural Product Research, 2021, v. 35, n. 15, p. 2602, doi. 10.1080/14786419.2019.1686368
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New butenolides with anti-inflammatory activity from Balanophora fungosa.
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- Natural Product Research, 2021, v. 35, n. 11, p. 1825, doi. 10.1080/14786419.2019.1645663
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Antioxidant Effects of Vitamin C on Biomedical UHMWPE Compounds.
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- Macromolecular Symposia, 2019, v. 383, n. 1, p. N.PAG, doi. 10.1002/masy.201800002
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Spiromesifen and spirotetramat resistance in field populations of Bemisia tabaci Gennadius in Spain.
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- Pest Management Science, 2019, v. 75, n. 1, p. 45, doi. 10.1002/ps.5144
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Flupyradifurone effectively manages whitefly Bemisia tabaci MED (Hemiptera: Aleyrodidae) and tomato yellow leaf curl virus in tomato.
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- Pest Management Science, 2017, v. 73, n. 8, p. 1574, doi. 10.1002/ps.4577
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Flupyradifurone: a brief profile of a new butenolide insecticide.
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- Pest Management Science, 2015, v. 71, n. 6, p. 850, doi. 10.1002/ps.3932
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Brønsted Base‐Catalyzed Direct 1,6‐Conjugate Addition of Butenolide to p‐Quinone Methides.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 7, p. 1, doi. 10.1002/ajoc.202300176
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Multiple Reaction Pathways Operating in the Mechanism of Vinylogous Mannich-Type Reaction Activated by a Water Molecule.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 1, p. 305, doi. 10.1002/asia.201301065
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Oxidative cyclization of #947;-alkylidene butenolides. Stereoselective preparation of spirolactones.
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- ARKIVOC: Online Journal of Organic Chemistry, 2012, p. 171
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Development and validation of a UHPLC-MS/MS method for the simultaneous determination of five bioactive flavonoids in rat plasma and comparative pharmacokinetic study after oral administration of Xiaochaihu Tang and three compatibilities.
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- Journal of Separation Science, 2017, v. 40, n. 9, p. 1896, doi. 10.1002/jssc.201601420
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Determination of Paracetamol in Presence of Ascorbic Acid in Pharmaceutical Products by Scanning Electrochemical Microscopy.
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- Electroanalysis, 2013, v. 25, n. 6, p. 1395, doi. 10.1002/elan.201300055
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Evolution of the nutritional composition of Hovenia dulcis Thunb. pseudofruit during the maturation process.
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- Fruits, 2015, v. 70, n. 3, p. 181, doi. 10.1051/fruits/2015011
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Mechanistic Insights into the Rh(I)/Rh<sub>2</sub>(II)‐Catalyzed Divergent Ring‐Opening of Cyclopropenes: A Computational Study.
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- ChemCatChem, 2020, v. 12, n. 22, p. 5656, doi. 10.1002/cctc.202001149
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Cytogenetic alterations induced by flupyradifurone, a new butenolide insecticide, in human lymphocytes.
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- Toxicology & Industrial Health, 2018, v. 34, n. 11, p. 737, doi. 10.1177/0748233718788989
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Genes for biosynthesis of butenolide-like signalling molecules in Streptomyces ghanaensis, their role in moenomycin production.
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- Russian Journal of Genetics, 2014, v. 50, n. 6, p. 563, doi. 10.1134/S1022795414060076
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Persistence of Flupyradifurone in Sandy Loam Soil and Effect of Organic Manure Amendment.
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- Pesticide Research Journal (09706763), 2020, v. 32, n. 2, p. 263, doi. 10.5958/2249-524X.2021.00007.8
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Dissipation Kinetics, Decontamination and Risk Assessment of Spiromesifen in/on Green Chillies.
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- Pesticide Research Journal (09706763), 2020, v. 32, n. 1, p. 12, doi. 10.5958/2249-524X.2020.00002.3
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Bioactive Aspergteroids G–J from Soft-Coral-Associated Symbiotic and Epiphytic Fungus Aspergillus terreus EGF7-0-1.
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- Bioengineering (Basel), 2023, v. 10, n. 7, p. 805, doi. 10.3390/bioengineering10070805
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Seasonal variation of ascorbic acid and nitrate levels in selected basil (Ocimum basilicum L.) varieties.
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- Horticultural Science, 2018, v. 45, n. 1, p. 47, doi. 10.17221/216/2016-HORTSCI
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Wild-Grown Romanian Helleborus purpurascens Approach to Novel Chitosan Phyto-Nanocarriers—Metabolite Profile and Antioxidant Properties.
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- Plants (2223-7747), 2023, v. 12, n. 19, p. 3479, doi. 10.3390/plants12193479
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Therapeutic Potential of Lindera obtusiloba : Focus on Antioxidative and Pharmacological Properties.
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- Plants (2223-7747), 2020, v. 9, n. 12, p. 1765, doi. 10.3390/plants9121765
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DETERMINATION OF ANTIOXIDANTS IN MEDICINAL HERBS.
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- Bulletin of the Transilvania University of Brasov, Series VI: Medical Sciences, 2011, v. 4, n. 2, p. 95
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Singlet-Oxygen Oxidation of 5-Hydroxymethylfurfural in Continuous Flow.
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- ChemSusChem, 2015, v. 8, n. 10, p. 1648, doi. 10.1002/cssc.201403182
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Modular Synthesis of Functionalized Butenolides by Oxidative Furan Fragmentation.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 3, p. 339, doi. 10.1002/ejoc.201901613
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High‐Yielding Diastereoselective syn‐Dihydroxylation of Protected HBO: An Access to D‐(+)‐Ribono‐1,4‐lactone and 5‐O‐Protected Analogues.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 7, p. 1600, doi. 10.1002/ejoc.201801780
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Enantioselective Approach to the Right-Hand Substructure of Solanoeclepin A.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 35, p. 5845, doi. 10.1002/ejoc.201601094
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Late-Stage Bromination Enables the Synthesis of Rubrolides B, I, K, and O.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 22, p. 3780, doi. 10.1002/ejoc.201600473
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Design and Synthesis of Butenolide-based Novel Benzyl Pyrrolones: Their TNF- α based Molecular Docking with In vivo and In vitro Anti-inflammatory Activity.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 619, doi. 10.1111/cbdd.12522
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Butanolides and Butenolides from a Marine-Derived Streptomyces sp. Exert Neuroprotective Activity through Activation of the TrkB Neurotrophin Receptor.
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- Marine Drugs, 2023, v. 21, n. 9, p. 465, doi. 10.3390/md21090465
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Butenolides from the Coral-Derived Fungus Aspergillius terreus SCSIO41404.
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- Marine Drugs, 2022, v. 20, n. 3, p. 212, doi. 10.3390/md20030212
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Open-Ring Butenolides from a Marine-Derived Anti-Neuroinflammatory Fungus Aspergillus terreus Y10.
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- Marine Drugs, 2018, v. 16, n. 11, p. 428, doi. 10.3390/md16110428
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