Works matching DE "ARYLSULFONATES"
Results: 50
Visible Light-Mediated Metal-Free Synthesis of Vinyl Sulfones from Aryl Sulfinates.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 9, p. 2050, doi. 10.1002/adsc.201500142
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Synthesis of 5-(Arylselanyl)-2-(arylsulfanyl)benzoates by [3+3] Cyclocondensation of 3-(Arylsulfanyl)-1-(silyloxy)buta-1,3-dienes with 2-(Arylselanyl)-3-(silyloxy)alk-2-en-1-ones.
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- Helvetica Chimica Acta, 2010, v. 93, n. 9, p. 1779, doi. 10.1002/hlca.201000110
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Synthesis and Antibacterial Activity of Some Aryloxyacetic Acid Derivatives Containing Aryl Sulfonate Moiety.
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- Online Turkish Journal of Health Sciences (OTJHS) / Online Türk Sağlık Bilimleri Dergisi, 2023, v. 8, n. 2, p. 260, doi. 10.26453/otjhs.1270936
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Palladium‐Catalyzed Direct α‐Arylation of Arylacetonitriles with Aryl Tosylates and Mesylates.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 12, p. 1912, doi. 10.1002/ejoc.202000176
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Room Temperature Ni<sup>0</sup>/PCy<sub>3</sub>-Catalyzed Coupling Reactions of Aryl Arenesulfonates with Bis(pinacolato)diboron.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 47, p. 7087, doi. 10.1002/ejoc.201701300
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Protective effects of new aryl sulfone derivatives against radiation-induced hematopoietic injury.
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- Journal of Radiation Research, 2020, v. 61, n. 3, p. 388, doi. 10.1093/jrr/rraa009
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Anti-HIV-1 activity of anionic polymers: a comparative study of candidate microbicides.
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- BMC Infectious Diseases, 2002, v. 2, n. 1, p. 27, doi. 10.1186/1471-2334-2-27
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A Novel Effect of Dioxin: Exposure during Pregnancy Severely Impairs Mammary Gland Differentiation1 The research in this article has been reviewed by the National Health and Environmental Effects Research Laboratory, U.S. EPA and approved for publication. Approval does not signify that the contents necessarily reflect the views and policies of the agency, nor does mention of trade names or commercial products constitute endorsement or recommendation for use.2Portions of these data were presented at the 42nd annual meeting of the Society of Toxicology, March 2003, Salt Lake City, UT.
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- Toxicological Sciences, 2004, v. 78, n. 2, p. 248, doi. 10.1093/toxsci/kfh062
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Effect of Herbicide Tribenuron methyl on pseudomonas aeruginosa isolated from Wheat Field in Thi-Qar Procince.
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- International Journal of Pharmaceutical Research (09752366), 2020, p. 4599, doi. 10.31838/ijpr/2020.SP2.575
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- Article
Reaction of N-acetyl- and N-[1-(arylsulfonylimino)ethyl]-1,4-benzoquinone imines with sodium arenesulfinates.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 9, p. 1283, doi. 10.1134/S1070428014090097
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2-Aroylcyclohexanones in the synthesis of 4-aryl-5,6,7,8-tetrahydroquinazolines and 3-aryl-4,5,6,7-tetrahydro-1 H-indoles.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 9, p. 1375, doi. 10.1134/S1070428014090243
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Reaction of N-arylsulfonyl-2(3)-arylsulfonylamino-substituted 1,4-benzoquinonimines with sodium arylsulfinates.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 2, p. 200, doi. 10.1134/S1070428014020109
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Benzazoles: I. Regioselective arylsulfonylation of benzimidazol-2-amine.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 1, p. 108, doi. 10.1134/S1070428013010181
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Synthesis of 1-(arylsulfonyl)pyrazolo[1,5- a]pyridines.
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- Russian Journal of Organic Chemistry, 2012, v. 48, n. 10, p. 1382, doi. 10.1134/S1070428012100223
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Synthesis of 2-arylsulfonylamino-3-phenyl-3-chloropropanoic acids.
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- Russian Journal of Organic Chemistry, 2012, v. 48, n. 5, p. 741, doi. 10.1134/S1070428012050193
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Reactions of N-arylsulfonylquinone imines with enamines.
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- Russian Journal of Organic Chemistry, 2011, v. 47, n. 8, p. 1169, doi. 10.1134/S1070428011080094
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Intramolecular electrophilic cyclization of functional derivatives of unsaturated Compounds: I. Synthesis of 5-arylsulfanyl-6-phenylpiperidin-2-ones from cinnamylacetamides and arylsulfenyl chlorides.
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- Russian Journal of Organic Chemistry, 2011, v. 47, n. 8, p. 1146, doi. 10.1134/S1070428011080057
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Divergent reactivities of 2-pyridyl sulfonate esters. Exceptionally mild access to alkyl bromides and 2-substituted pyridines.
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- Canadian Journal of Chemistry, 2021, v. 99, n. 7, p. 603, doi. 10.1139/cjc-2020-0510
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Investigation of Chemoselective Reaction of 2-Amino-8-hydroxyquinoline with Arylsulfonylchloride Derivatives.
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- Synthetic Communications, 2009, v. 39, n. 8, p. 1378, doi. 10.1080/00397910802527730
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Decarboxylative Aminomethylation of Aryl- and Vinylsulfonates through Combined Nickel- and Photoredox-Catalyzed Cross-Coupling.
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- Chemistry - A European Journal, 2016, v. 22, n. 46, p. 16437, doi. 10.1002/chem.201604452
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Competing Pathways in the Photogeneration of Didehydrotoluenes from (Trimethylsilylmethyl)aryl Sulfonates and Phosphates.
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- Chemistry - A European Journal, 2014, v. 20, n. 52, p. 17572, doi. 10.1002/chem.201404787
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Synthesis and In Vitro Human Carbonic Anhydrase I and II Inhibition Properties of Some Novel Hydrazone Compounds Containing an Aryl Sulfonate Moiety.
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- Erzincan University Journal of Science & Technology, 2022, v. 15, n. 2, p. 659, doi. 10.18185/erzifbed.1132001
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Conductivity Enhancement of Graphene and Graphene Derivatives by Silver Nanoparticles.
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- Applied Sciences (2076-3417), 2023, v. 13, n. 13, p. 7600, doi. 10.3390/app13137600
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Cladocers, Copepods and Rotifers in rice-fish culture handled with metsulfuron-methyl and azimsulfuron herbicides and carbofuran insecticide.
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- Ciência Rural, 2008, v. 38, n. 8, p. 2097, doi. 10.1590/S0103-84782008000800001
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Enantioselective Intermolecular Heck and Reductive Heck Reactions of Aryl Triflates, Mesylates, and Tosylates Catalyzed by Nickel.
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- Angewandte Chemie, 2021, v. 133, n. 6, p. 2864, doi. 10.1002/ange.202011036
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Quantum Dot‐Catalyzed Photoreductive Removal of Sulfonyl‐Based Protecting Groups.
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- Angewandte Chemie, 2020, v. 132, n. 33, p. 14195, doi. 10.1002/ange.202005074
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Silver‐Promoted Oxidative Benzylic C−H Trifluoromethoxylation.
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13450, doi. 10.1002/ange.201807144
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Direct Dehydroxytrifluoromethoxylation of Alcohols.
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- Angewandte Chemie, 2018, v. 130, n. 1, p. 298, doi. 10.1002/ange.201711050
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Synthesis and crystal structure of three new bismuth(III) arylsulfonatocarboxylates.
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- Zeitschrift für Kristallographie. Crystalline Materials, 2017, v. 232, n. 1-3, p. 245, doi. 10.1515/zkri-2016-1980
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Nickel-Catalyzed Mizoroki-Heck Reaction of Aryl Sulfonates and Chlorides with Electronically Unbiased Terminal Olefins: High Selectivity for Branched Products.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 7, p. 1858, doi. 10.1002/anie.201308391
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Desulfinative and denitrogenative palladium‐catalyzed cross‐coupling of arylsulfonyl hydrazides with aryl diazonium salts.
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- Applied Organometallic Chemistry, 2018, v. 32, n. 11, p. N.PAG, doi. 10.1002/aoc.4484
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Palladium-catalyzed reductive homocoupling of aryl sulfonates via cleavage of C─O bond at room temperature.
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- Applied Organometallic Chemistry, 2017, v. 31, n. 9, p. n/a, doi. 10.1002/aoc.3705
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Arylsulfonium Salt Treatment Of Mercerized Cotton Fabric.
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- Textile Chemist & Colorist, 1987, v. 19, n. 6, p. 19
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Synthesis of vicinal 2-aryl(hetaryl)-2-[aryl(hetaryl)-sulfonyl]-ethanamines.
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- Ukrainica Bioorganica Acta, 2009, v. 7, n. 2, p. 3
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Photohomolysis and Photoheterolysis in Aryl Sulfonates and Aryl Phosphates.
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- Chemistry - A European Journal, 2021, v. 27, n. 20, p. 6315, doi. 10.1002/chem.202005426
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Cover Feature: Metal‐ and Reagent‐Free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi‐Component Reaction (Chem. Eur. J. 38/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 38, p. 8315, doi. 10.1002/chem.202002881
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- Article
Metal‐ and Reagent‐Free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi‐Component Reaction.
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- Chemistry - A European Journal, 2020, v. 26, n. 38, p. 8358, doi. 10.1002/chem.202001180
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Generation of Organozinc Reagents by Nickel Diazadiene Complex Catalyzed Zinc Insertion into Aryl Sulfonates.
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- Chemistry - A European Journal, 2020, v. 26, n. 1, p. 176, doi. 10.1002/chem.201904545
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Aryl Sulfonates in Inversions at Secondary Carbohydrate Hydroxyl Groups: A New and Improved Route Toward 3-Azido-3-deoxy-β-d-galactopyranosides.
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- Journal of Carbohydrate Chemistry, 2015, v. 34, n. 8, p. 490, doi. 10.1080/07328303.2015.1105248
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Leaching behaviour of metsulfuron in two texturally different soils.
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- Environmental Monitoring & Assessment, 2009, v. 154, n. 1-4, p. 111, doi. 10.1007/s10661-008-0381-8
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- Article
Nickel-Catalyzed Mizoroki-Heck Reaction of Aryl Sulfonates and Chlorides with Electronically Unbiased Terminal Olefins: High Selectivity for Branched Products.
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- Angewandte Chemie, 2014, v. 126, n. 7, p. 1889, doi. 10.1002/ange.201308391
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- Article
Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignards with Aryl Chlorobenzenesulfonates.
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- Molecules, 2021, v. 26, n. 19, p. 5895, doi. 10.3390/molecules26195895
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Convenient Synthesis of Ferrocenylethynyl Ketones via Carbonylative Coupling of Ferrocenylethyne with Aryl Iodides by Using Water as Solvent.
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- Catalysis Letters, 2009, v. 127, n. 1/2, p. 152, doi. 10.1007/s10562-008-9661-8
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Aryl sulfonate based anticancer alkylating agents.
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- Pakistan Journal of Pharmaceutical Sciences, 2018, v. 31, p. 1081
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Unprecedented High Probe-Reported Polarity of Deep Eutectic Solvents Composed of Lanthanide Salts and Urea.
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- Liquids (2673-8015), 2024, v. 4, n. 3, p. 505, doi. 10.3390/liquids4030028
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Microwave-Assisted Synthesis and Antimicrobial Activity of 3-(Arylsulfanyl)-4-hydroxy-2H-chromen-2-ones.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 10, p. 2149, doi. 10.1134/S1070363218100201
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Solvent effect on the reactivity of arylsulfanyl radicals.
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- Russian Journal of General Chemistry, 2011, v. 81, n. 6, p. 1146, doi. 10.1134/S1070363211060120
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Synthesis of Novel Substituted Indazoles via Nucleophilic Substitution of Hydrogen (S <sub>N</sub>H).
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- Heteroatom Chemistry, 2015, v. 26, n. 5, p. 374, doi. 10.1002/hc.21270
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Study on distribution coefficient of bromine ions from aqueous solution on ion exchange resins Duolite A-161 and Duolite A-162.
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- Colloid Journal, 2010, v. 72, n. 6, p. 874, doi. 10.1134/S1061933X10060207
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Inorganic and organomodified nano-montmorillonite dispersions for use as supplementary cementitious materials – a novel theory based on nanostructural studies.
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- Nanocomposites, 2017, v. 3, n. 1, p. 2, doi. 10.1080/20550324.2017.1315210
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