Works matching DE "SULFONYL chlorides"
Results: 221
Poly(HEMA) Microbeads with Multi Amine Surface Functions for Reversible Metal Complex Formation.
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- Macromolecular Symposia, 2016, v. 364, n. 1, p. 32, doi. 10.1002/masy.201500126
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Reaction of 5-Hydroxymethyl-6-Methyluracil with Toluenesulfonyl Chloride or Methanesulfonyl Chloride and Tertiary Amines.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 4, p. 714, doi. 10.1007/s10600-017-2097-x
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Synthesis and molecular structure of 4-{[6-((2SR,4SR)-4-acetyl-4-methylpyrrolidin-2-yl)-2-(4-cyanophenoxy)pyrimidin-4-yl]oxy}-3,5-dimethylbenzonitrile and 4-[(6-{(2SR,4SR)-4-acetyl-1-[(4-bromophenyl)sulfonyl]-4-methylpyrrolidin-2-yl}-2-(4-cyanophenoxy)pyrimidin-4-yl)oxy]-3,5-dimethylbenzonitrile
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- Chemistry of Heterocyclic Compounds, 2022, v. 58, n. 1, p. 64, doi. 10.1007/s10593-022-03057-y
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The tandem Dimroth rearrangement and sulfonylation/acylation as regioselective method for the synthesis of 5-arylamino-2-sulfonyland 2-acyl-5-arylamino-1,2,3-triazole-4-carbothioamides.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 10, p. 1341, doi. 10.1007/s10593-020-02820-3
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1-Sulfonyl-1,2,3-triazoles as promising reagents in the synthesis of nitrogen-containing linear and heterocyclic structures (microreview).
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 4, p. 216, doi. 10.1007/s10593-016-1865-z
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Heterocyclization of N-(chlorosulfonyl)imidoyl chlorides with anilines, a new method of synthesis of 1,2,4-benzothiadiazine 1,1-dioxides.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 4, p. 267, doi. 10.1007/s10593-016-1873-z
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Reaction of 2-Aryl-4-Cyano-1,3-Oxazole-5-Sulfonyl Chlorides With 5-Amino-1 H-Pyrazoles and 5-Amino-1 H-1,2,4-Triazole.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 1, p. 76, doi. 10.1007/s10593-014-1450-2
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Methods of Sultam Synthesis.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 1, p. 39, doi. 10.1007/s10593-013-1231-3
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Synthesis, characterization and electrochemical properties of some biologically important indole-based-sulfonamide derivatives.
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- BMC Chemistry, 2020, v. 14, n. 1, p. 1, doi. 10.1186/s13065-020-00691-5
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Synthesis and bioactivity of several new hetaryl sulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 137, doi. 10.1080/14756366.2016.1238367
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Synthesis of novel sulfonamide analogs containing sulfamerazine/sulfaguanidine and their biological activities.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1005, doi. 10.3109/14756366.2015.1079183
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Homolytic Decomposition of Sulfonyl Chlorides.
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- Doklady Chemistry, 2018, v. 480, n. 1, p. 93, doi. 10.1134/S0012500818050063
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Copolymerization of tetrafluoroethylene with perfluoro(3,6-dioxa-4-methyl-7-octene)sulfonyl fluoride in a water-emulsion medium.
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- Doklady Chemistry, 2011, v. 437, n. 1, p. 66, doi. 10.1134/S0012500811030086
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Synthesis, spectroscopic, DFT calculations, biological activity, SAR, and molecular docking studies of novel bioactive pyridine derivatives.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-42714-w
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Synthesis, spectroscopic, DFT calculations, biological activity, SAR, and molecular docking studies of novel bioactive pyridine derivatives.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-42714-w
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Yeni Benzensülfonamitler ve Benzamitlerin Sentezi, Karbonik Anhidraz ve Kolinerjik Etkilerinin İncelenmesi.
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- Journal of the Institute of Science & Technology / Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2023, v. 13, n. 3, p. 1814, doi. 10.21597/jist.1278301
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Oxidative cleavage and ammoxidation of organosulfur compounds via synergistic Co-Nx sites and Co nanoparticles catalysis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38614-2
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One-pot synthesis of sulfonylhydrazones from sulfonyl chloride, hydrazine hydrate and vinyl azide in water.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 10, p. 2713, doi. 10.1007/s13738-021-02226-8
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Ir-catalyzed C-S coupling of quinones with sulfonyl chloride.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 10, p. 1797, doi. 10.1007/s13738-016-0897-8
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4‐(Di‐/Trifluoromethyl)‐2‐heterabicyclo[2.1.1]hexanes: Advanced Fluorinated Phenyl Isosteres and Proline analogues.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 47, p. 6580, doi. 10.1002/ejoc.202100414
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Synthesis of Symmetrical Thiosulfonates via Cu(OTf)<sub>2</sub>‐Catalyzed Reductive Homocoupling of Arenesulfonyl Chlorides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 43, p. 5880, doi. 10.1002/ejoc.202101101
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Temperature‐Controlled Chemoselective Synthesis of Thiosulfonates and Thiocyanates: Novel Reactivity of KXCN (X=S, Se) towards Organosulfonyl Chlorides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 38, p. 5359, doi. 10.1002/ejoc.202101031
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One‐Pot Synthesis of Thiocarbamates.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 31, p. 4508, doi. 10.1002/ejoc.202100858
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I<sub>2</sub>‐Promoted Direct C−H Sulfenylation of Isoquinolin‐1(2H)‐ones with Sulfonyl Chlorides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 1, p. 117, doi. 10.1002/ejoc.202001371
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Amino Acid‐Based Dithiocarbamates as Efficient Intermediates for Diversity‐Oriented Synthesis of Thiazoles.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 38, p. 6081, doi. 10.1002/ejoc.202001050
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A Base‐Controlled Reaction of 2‐Cyanoacetamidines (3,3‐Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4‐Methylene‐1,2,3‐triazole‐5‐imines.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 24, p. 3688, doi. 10.1002/ejoc.202000453
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Synthesis of Sulfonyl Fluorides from Sulfonamides.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 17, p. 2497, doi. 10.1002/ejoc.202000022
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3‐Carboxy‐/3‐Aminobicyclo[1.1.1]pentane‐Derived Sulfonamides and Sulfonyl Fluorides – Advanced Bifunctional Reagents for Organic Synthesis and Drug Discovery.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 15, p. 2210, doi. 10.1002/ejoc.202000303
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Air‐Induced One‐Pot Synthesis of N‐Sulfonylformamidines from Sulfonyl Chlorides, NaN<sub>3</sub>, and Tertiary/Secondary Amines.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 35, p. 6071, doi. 10.1002/ejoc.201901048
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General Synthesis of Industrial Cephalosporin‐Based Antibiotics Through Amidation with Tosyl Chloride as a Coupling Reagent.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 20, p. 3259, doi. 10.1002/ejoc.201900277
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Synthesis of (Poly)halo‐Substituted Diarylsulfones through Palladium‐Catalyzed C–H Bond Sulfonylation Using (Poly)Halobenzenesulfonyl Chlorides.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 44, p. 6114, doi. 10.1002/ejoc.201800819
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Biochemical surface modifications to titanium implants using the tresyl chlorideactivated method.
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- Dental Materials Journal, 2015, v. 34, n. 6, p. 725, doi. 10.4012/dmj.2015-067
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Arylsulfonyl- N-2-carbamoylguanidines in synthesis of hetarylsulfonamides and characterization of the compounds obtained.
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- Petroleum Chemistry, 2014, v. 54, n. 3, p. 229, doi. 10.1134/S0965544114030074
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Crystal structure of 3-ferrocenylsulfonyl-2-(4-methoxyphenyl)-3H-imidazo[4,5-b]pyridine, C<sub>23</sub>H<sub>19</sub>FeN<sub>3</sub>O<sub>3</sub>S.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2016, v. 231, n. 2, p. 641, doi. 10.1515/ncrs-2015-0223
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The influence of amino chain length and calcium lignosulfonate modification on lignosulfonamides flammability and thermal stability.
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- Polimery, 2023, v. 68, n. 10, p. 544, doi. 10.14314/polimery.2023.10.4
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New Synthetic Methods for Pyrazolesulfonyl Chlorides as Drug Precursors.
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- Pharmaceutical Chemistry Journal, 2017, v. 50, n. 11, p. 768, doi. 10.1007/s11094-017-1528-0
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Synthesis of n-methyl-3-carboxy-2-chloro-dibenzo[ c,f][1,4,5]oxa-thiazepine s,s-dioxide and its derivatives.
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- Chemistry of Heterocyclic Compounds, 2009, v. 45, n. 11, p. 1391, doi. 10.1007/s10593-010-0438-9
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BENZAMINE DERIVATIVES: SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL ACTIVITY STUDY.
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- Chemical Problems / Kimya Problemləri, 2024, v. 22, n. 4, p. 411, doi. 10.32737/2221-8688-2024-4-411-435
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MNPs@PBI-CuBr<sub>2</sub> Nanocomposite Catalyzed One-Pot Three-Component Reaction of 2-Aminobenzoazoles, Sulfonyl Chloride and Aryl Iodides.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 2, p. 1151, doi. 10.1080/10406638.2023.2186447
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Synthesis and Evaluation of Novel (5S)-5-(Aminomethyl)-3-[4-(6,7-Dihydrothieno[3,2-c]Pyridin-5(4H)-yl)Phenyl]-1,3-Oxazolidin-2-One Derivatives as Potent Antimicrobial Agents.
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- Polycyclic Aromatic Compounds, 2023, v. 43, n. 7, p. 6470, doi. 10.1080/10406638.2022.2118324
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Synthesis and Characterization of Novel N-Propylaniline-Phenylpiperazine Sulfonamide and Urea Derivatives.
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- Polycyclic Aromatic Compounds, 2022, v. 42, n. 8, p. 5767, doi. 10.1080/10406638.2021.1954040
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Synthesis of Novel Indenopyrimidine Sulfonamides from Indenopyrimidine-2-Amines via S–N Bond Formation.
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- Polycyclic Aromatic Compounds, 2022, v. 42, n. 4, p. 1828, doi. 10.1080/10406638.2020.1809470
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Search for new biologically active compounds based on 6-methyluracil-5-sulfochloride and alcohols.
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- Technology Audit & Production Reserves, 2018, v. 39, n. 3, p. 4, doi. 10.15587/2312-8372.2018.124272
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- Article
Nucleophilic Substitution in 6-Chloro-2-(2-cyano-phenoxy)quinoxalines and Antibacterial Activity of Phenoxychloroquinoxaline Derivatives.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 4, p. 647, doi. 10.1134/S1070428021040217
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- Article
Synthesis of New Sulfonamides Based on β-Pinene.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 3, p. 405, doi. 10.1134/S1070428020030070
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- Article
Synthesis and Oxidation of Myrtanethiol and Its Functional Derivatives with Chlorine Dioxide.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 10, p. 1469, doi. 10.1134/S107042801910004X
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Synthesis of 2,5-dihydroimidazo[4,5- e][1,2,3]thiadiazine 1,1-dioxides-Derivatives of a novel heterocyclic system.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 12, p. 1890, doi. 10.1134/S107042801712020X
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New synthesis of 3,5-diaryl-1,2,4-oxadiazoles containing a sulfonyl chloride or sulfonamide group.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 7, p. 988, doi. 10.1134/S1070428015070167
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N-Propargyltrifluoromethanesulfonamide.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 5, p. 747, doi. 10.1134/S1070428014050212
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2,2-Bis(methoxy- and ethoxy-NNO-azoxy)propane-1,3-diol sulfonates.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 5, p. 631, doi. 10.1134/S1070428014050030
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- Article