Works matching DE "DIAMIDES"
Results: 213
Synthesis and Antioxidant Activity of N-Substituted Diamides Based on Ethyl N-(2-Allyl-2-arylpent-4-en-1-yl)oxamate.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 11, p. 2117, doi. 10.1134/S1070428024110046
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Macrophage Recognition of Thiol-Group Oxidized Cells: Recognition of Carbohydrate Chains by Macrophage Surface Nucleolin as Apoptotic Cells.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 11, p. 2068, doi. 10.1271/bbb.120413
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Adaptive evolution of Corynebacterium glutamicum resistant to oxidative stress and its global gene expression profiling.
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- Biotechnology Letters, 2013, v. 35, n. 5, p. 709, doi. 10.1007/s10529-012-1135-9
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Preparation, anticholinesterase activity, and docking study of new 2-butenediamide and oxalamide derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 4, p. 671, doi. 10.3109/14756366.2014.959947
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Identification of differentially expressed miRNAs associated with diamide detoxification pathways in Spodoptera frugiperda.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-54771-w
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Identification of differentially expressed miRNAs associated with diamide detoxification pathways in Spodoptera frugiperda.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-54771-w
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X-ray powder diffraction data for (1R, 5S, 7R)-7-[(S)-4-benzyl-4,5-dihydrooxazole-2-yl]-1,5,7-trimethyl-3-azabicyclo-[3.3.1]-nonane-2,4-dione, another new chiral Kemp's acid diamide.
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- Powder Diffraction, 2012, v. 27, n. 4, p. 273, doi. 10.1017/S088571561200067X
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Synthesis, crystal structure and larvicidal activity of novel diamide derivatives against Culex pipiens.
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- Chemistry Central Journal, 2012, v. 6, n. 1, p. 99, doi. 10.1186/1752-153X-6-99
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Efficacy of indoor residual spraying with broflanilide (TENEBENAL), a novel meta-diamide insecticide, against pyrethroid-resistant anopheline vectors in northern Tanzania: An experimental hut trial.
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- PLoS ONE, 2021, v. 16, n. 3, p. 1, doi. 10.1371/journal.pone.0248026
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Prolinol as a Chiral Auxiliary in Organophosphorus Chemistry.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 12, p. 1931, doi. 10.1002/ejoc.202100196
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Mechanochemical Solvent‐Free Conditions for the Synthesis of Pillar[5]arene‐Containing [2]Rotaxanes.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 21, p. 3401, doi. 10.1002/ejoc.201900153
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Solvent Extraction: Structure of the Liquid-Liquid Interface Containing a Diamide Ligand.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 32, p. 9326, doi. 10.1002/anie.201603395
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Successful application of anthranilic diamides in preventing small hive beetle (Coleoptera: Nitidulidae) infestation in honey bee (Hymenoptera: Apidae) colonies.
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- Journal of Insect Science, 2023, v. 23, n. 6, p. 1, doi. 10.1093/jisesa/iead096
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Characterization of the Ryanodine Receptor Gene With a Unique 30-UTR and Alternative Splice Site From the Oriental Fruit Moth.
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- Journal of Insect Science, 2016, v. 16, n. 1, p. 1, doi. 10.1093/jisesa/iev148
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Density functional theory insight into Eu(III) and Am(III) complexes with two 2,6-dicarboxypyridine diamide-type ligands.
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- Journal of Structural Chemistry, 2017, v. 58, n. 4, p. 675, doi. 10.1134/S0022476617040059
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TETRANILIPROLE- NEW DIAMIDE INSECTICIDE MOLECULE FEATURING NOVEL MODE OF ACTION AGAINST SOYBEAN INSECT PESTS.
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- Biochemical & Cellular Archives, 2017, v. 17, n. 2, p. 801
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Synthesis and Antimicrobial Activities of Some New Bis(Schiff Bases) and Their Triazole-Based Lariat Macrocycles.
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- Polycyclic Aromatic Compounds, 2022, v. 42, n. 5, p. 2751, doi. 10.1080/10406638.2020.1852272
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Synthesis, Characterization, and Exploration of Antimicrobial Activity of Copper Complex of Diamide Derivative of p-tert-butylcalix[4]arene.
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- Polycyclic Aromatic Compounds, 2017, v. 37, n. 5, p. 362, doi. 10.1080/10406638.2015.1125375
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Catalytic Cyclothiomethylation of Diamides and Dihydrazides of (Thio)carbonic Acid Using Bis(dimethylamino)methane, H2S, and Na2S·9H2O.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 2, p. 276, doi. 10.1134/S1070428020020165
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Synthesis of Dicarboxylic Acid Amides and Diamides on the Basis of [4-(4-Methoxyphenyl)tetrahydro-2H-pyran-4-yl]methanamine.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 6, p. 886, doi. 10.1134/S1070428018060106
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Synthesis of diamides from 1,4-benzodioxane-2- and isochroman-1-carboxylic acids.
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- Russian Journal of Organic Chemistry, 2012, v. 48, n. 7, p. 972, doi. 10.1134/S1070428012070147
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Conformational Analysis of Bis[N-alkyl-N-(2-diphenylphosphorylethyl)]amides of Diglycolic Acid.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 12, p. 2590, doi. 10.1134/S1070363222120064
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FIELD RESISTANCE TO CYANTRANILIPROLE IN PLUTELLA XYLOSTELLA.
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- Indian Journal of Entomology, 2023, v. 85, n. 4, p. 908, doi. 10.55446/IJE.2023.942
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SUSCEPTIBILITY OF DIAMOND BACK MOTH PLUTELLA XYLOSTELLA (L.) TO DIAMIDE INSECTICIDES.
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- Indian Journal of Entomology, 2022, v. 84, n. 4, p. 927, doi. 10.55446/IJE.2021.132
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CHARACTERIZATION OF THE RESISTANCE OF Chrysodeixis includens TO DIAMIDES.
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- Revista Caatinga, 2022, v. 35, n. 2, p. 288, doi. 10.1590/1983-21252022v35n205rc
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ELECTROCHEMICAL INVESTIGATION OF THE INHIBITING EFFECT EXERTED BY THE SULFURIC ACID DIAMIDE ON BRONZE CORROSION.
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- Studia Universitatis Babes-Bolyai, Chemia, 2016, v. 61, n. 3 Tom1, p. 125
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A Distibene with Extremely Long Sb=Sb Distance and Related Heavier Dipnictenes from Salt‐Free Metathesis Reactions.
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- European Journal of Inorganic Chemistry, 2024, v. 27, n. 10, p. 1, doi. 10.1002/ejic.202300586
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Impact of agricultural adjuvants on the toxicity of the diamide insecticides chlorantraniliprole and flubendiamide on different life stages of the navel orangeworm (Amyelois transitella).
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- Journal of Pest Science, 2018, v. 91, n. 3, p. 1127, doi. 10.1007/s10340-018-0959-z
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A four-year survey on insecticide resistance and likelihood of chemical control failure for tomato leaf miner Tuta absoluta in the European/Asian region.
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- Journal of Pest Science, 2018, v. 91, n. 1, p. 421, doi. 10.1007/s10340-017-0900-x
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First report of Tuta absoluta resistance to diamide insecticides.
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- Journal of Pest Science, 2015, v. 88, n. 1, p. 9, doi. 10.1007/s10340-015-0643-5
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Chromatin and stress.
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- Nature Genetics, 2012, v. 44, n. 9, p. 967, doi. 10.1038/ng.2403
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Design, Synthesis, and Biological Screening of Novel Anthranilic Diamides.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 3, p. 865, doi. 10.1002/jhet.2351
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Synthesis of Novel Benzo-substituted Macrocyclic Ligands Containing Thienothiophene Subunits.
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- Journal of Heterocyclic Chemistry, 2014, v. 51, p. E34, doi. 10.1002/jhet.2012
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Synthesis of New Aza Macrocyclic Diamides 2,2′-Diaminodiphenyl Sulfide Using Crab-Like Method.
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- Journal of Heterocyclic Chemistry, 2012, v. 49, n. 3, p. 499, doi. 10.1002/jhet.775
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The formation of squaramic acids and squaryl diamides by the reaction of squaric acid with alkyl isocyanides.
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- Journal of Chemical Research, 2013, v. 37, n. 6, p. 342, doi. 10.3184/174751913X13677757448841
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E. coli propionyl-CoA synthetase is regulated in vitro by an intramolecular disulfide bond.
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- Applied Biochemistry & Microbiology, 2012, v. 48, n. 3, p. 257, doi. 10.1134/S0003683812030040
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Covalently assembled resorcin[4]arenes and molecular tweezers: a chiral recognition rationale by NMR.
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- Supramolecular Chemistry, 2016, v. 28, n. 7/8, p. 647, doi. 10.1080/10610278.2015.1111373
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Picolinic diamide pincers for transition metal complexation and their electrochemical properties.
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- Supramolecular Chemistry, 2014, v. 26, n. 10-12, p. 843, doi. 10.1080/10610278.2014.883076
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Pre-organisation or a hydrogen bonding mismatch: silver(I) diamide ligand coordination polymers versus discrete metallo-macrocyclic assemblies.
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- Supramolecular Chemistry, 2012, v. 24, n. 8, p. 627, doi. 10.1080/10610278.2012.699052
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A case study of solid state inhibition lock opening of pyridine N-oxide in dicarboxylic acid recognition.
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- Supramolecular Chemistry, 2012, v. 24, n. 4, p. 264, doi. 10.1080/10610278.2012.656123
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Application of Dispersive Solid-Phase Extraction (SPE) Based on Carbon S for the Determination of Multiple Residues of Diamine Pesticides in Vegetables.
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- Analytical Letters, 2024, v. 57, n. 12, p. 1933, doi. 10.1080/00032719.2023.2281588
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Novel diamide ligands with a central carbonyl group and their comparative evaluation with the diglycolamide ligand: synthesis, extraction, DFT and chromatographic studies.
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- Radiochimica Acta, 2019, v. 107, n. 12, p. 1133, doi. 10.1515/ract-2019-3102
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Evaluation of several novel diamide based ligands for selective extraction of tetravalent plutonium.
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- Radiochimica Acta, 2017, v. 105, n. 4, p. 303, doi. 10.1515/ract-2016-2675
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Am(III) separation from acidic solutions by diamides of dipicolinic acid.
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- Radiochimica Acta, 2013, v. 101, n. 12, p. 753, doi. 10.1524/ract.2013.2084
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Stable expression and functional characterisation of the diamondback moth ryanodine receptor G4946E variant conferring resistance to diamide insecticides.
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- Scientific Reports, 2015, p. 14680, doi. 10.1038/srep14680
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Linear Diamides Derivative-Nucleated Biodegradable Poly(ethylene succinate) Polyester: Crystallization Kinetics and Aggregated Structure Manipulated by Hydrogen Bond Interaction.
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- Journal of Polymers & the Environment, 2021, v. 29, n. 11, p. 3605, doi. 10.1007/s10924-021-02141-2
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Toxicity and effects on anuran tadpole metamorphosis of the anthranilic diamide insecticides chlorantraniliprole and cyantraniliprole.
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- Journal of Toxicology & Environmental Health: Part A, 2023, v. 86, n. 15, p. 518, doi. 10.1080/15287394.2023.2224366
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Synthesis and characterization of poly(ester amides)s with a variable ratio of branched odd diamide units.
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- Journal of Applied Polymer Science, 2014, v. 131, n. 7, p. n/a, doi. 10.1002/app.40102
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Synthesis and characterization of di-polyester diamides.
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- Journal of Applied Polymer Science, 2012, v. 126, n. 1, p. 216, doi. 10.1002/app.36748
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A prelude to building mathematical models for polypeptide folding: analysis on the conformational potential energy hypersurface cross-sections of N-acetyl-glycyl-glycine-N′-methylamide.
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- Canadian Journal of Chemistry, 2018, v. 96, n. 10, p. 912, doi. 10.1139/cjc-2018-0017
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