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Journal articles on the topic 'Sulfonium ion'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Kooter, Ingeborg M., Nicole Moguilevsky, Alex Bollen, et al. "The Sulfonium Ion Linkage in Myeloperoxidase." Journal of Biological Chemistry 274, no. 38 (1999): 26794–802. http://dx.doi.org/10.1074/jbc.274.38.26794.

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2

Kumar, Ashwani, and Chullikkattil P. Pradeep. "Aromatic sulfonium polyoxomolybdates: tuning the photochromic properties through substitutions on the counter ion moiety." CrystEngComm 20, no. 19 (2018): 2733–40. http://dx.doi.org/10.1039/c8ce00345a.

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A series of aromatic sulfonium Keggin hybrids have been developed which exhibited excellent photochromic properties under UV irradiation. The photo-coloration speed of these hybrids could be fine-tuned by changing the substituents on the sulfonium counter ion moiety.

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3

Melnyk, Michael C., and Kenneth L. Busch. "POSITIVE ION LIQUID SECONDARY ION MASS SPECTRA OF AROMATIC SULFONIUM SALTS." Phosphorus, Sulfur, and Silicon and the Related Elements 122, no. 1 (1997): 287–98. http://dx.doi.org/10.1080/10426509708043517.

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4

Ardiansah, Bayu, Hiroki Tanimoto, Takenori Tomohiro, Tsumoru Morimoto, and Kiyomi Kakiuchi. "Sulfonium ion-promoted traceless Schmidt reaction of alkyl azides." Chemical Communications 57, no. 70 (2021): 8738–41. http://dx.doi.org/10.1039/d1cc02770k.

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Schmidt reaction by sulfonium ions is described. The bond scission reaction through 1,2-migration was achieved without any trace of the activators. The one-pot substitution reactions were also demonstrated.

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5

Lewis, Charles A., and Richard Wolfenden. "Sulfonium Ion Condensation: The Burden Borne by SAM Synthetase." Biochemistry 57, no. 26 (2018): 3549–51. http://dx.doi.org/10.1021/acs.biochem.8b00477.

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6

Mensink, Rens A., Hidde Elferink, Paul B. White, Nathalie Pers, Floris P. J. T. Rutjes, and Thomas J. Boltje. "A Study on Stereoselective Glycosylations via Sulfonium Ion Intermediates." European Journal of Organic Chemistry 2016, no. 27 (2016): 4656–67. http://dx.doi.org/10.1002/ejoc.201600898.

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7

Maji, Tanmoy, Sanjib Banerjee, Avijit Bose, and Tarun K. Mandal. "A stimuli-responsive methionine-based zwitterionic methacryloyl sulfonium sulfonate monomer and the corresponding antifouling polymer with tunable thermosensitivity." Polymer Chemistry 8, no. 20 (2017): 3164–76. http://dx.doi.org/10.1039/c7py00460e.

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This report describes a dual pH- and thermo-responsive methionine-based zwitterionic methacryloyl sulfonium sulfonate monomer and the corresponding zwitterionic antifouling polymer with ion-induced tunable thermosensitivity.

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8

Ghavami, Ahmad, Blair D. Johnston, Matthew D. Maddess, et al. "Synthesis of 1,4-anhydro-D-xylitol heteroanalogues of the naturally occurring glycosidase inhibitor salacinol and their evaluation as glycosidase inhibitors." Canadian Journal of Chemistry 80, no. 8 (2002): 937–42. http://dx.doi.org/10.1139/v02-078.

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The syntheses of two 1,4-anhydro-D-xylitol heteroanalogues (8 and 9) of the naturally occurring sulfonium ion, salacinol (3), containing a sulfur or nitrogen atom in the ring are described. Salacinol (3) is one of the active principles in the aqueous extracts of Salacia reticulata that are traditionally used in Sri Lanka and India for the treatment of Type 2 diabetes. The synthetic strategy relies on the nucleophilic attack of sulfur or nitrogen analogues of 1,4-anhydro-D-xylitol at the least-hindered carbon of 2,4-O-benzylidene-L-erythritol-1,3-cyclic sulfate. The sulfonium ion 8 inhibited ba

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9

Kramer, Jessica R., Nathan W. Schmidt, Kristine M. Mayle, Daniel T. Kamei, Gerard C. L. Wong, and Timothy J. Deming. "Reinventing Cell Penetrating Peptides Using Glycosylated Methionine Sulfonium Ion Sequences." ACS Central Science 1, no. 2 (2015): 83–88. http://dx.doi.org/10.1021/acscentsci.5b00054.

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10

Lequan, M., R. M. Lequan, P. Delhaes, and C. Hauw. "New Examples of Ternary Organic Conductors: Sulfonium Ion Radical Salts." Molecular Crystals and Liquid Crystals 120, no. 1 (1985): 353–56. http://dx.doi.org/10.1080/00268948508075818.

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11

Boltje, Thomas J., Jin-Hwan Kim, Jin Park та Geert-Jan Boons. "Stereoelectronic Effects Determine Oxacarbenium vs β-Sulfonium Ion Mediated Glycosylations". Organic Letters 13, № 2 (2011): 284–87. http://dx.doi.org/10.1021/ol1027267.

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12

Morgan, David L., Casey D. Stokes, Michelle A. Meierhoefer, and Robson F. Storey. "Sulfonium Ion Adducts from Quasiliving Polyisobutylene and Mono- or Disulfides." Macromolecules 42, no. 7 (2009): 2344–52. http://dx.doi.org/10.1021/ma802812m.

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13

Harvey, Jeremy N., and Heinz G. Viehe. "3-Thio-Claisen rearrangement of the allyl vinyl sulfonium ion." Journal of the Chemical Society, Chemical Communications, no. 22 (1995): 2345. http://dx.doi.org/10.1039/c39950002345.

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14

Duffin, Kevin L., and Kenneth L. Busch. "Positive secondary ion mass spectra of sulfonium and iodonium salts." International Journal of Mass Spectrometry and Ion Processes 74, no. 2-3 (1986): 141–52. http://dx.doi.org/10.1016/0168-1176(86)85001-7.

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15

Pritzkow, Hans, Klaus Rall, and Wolfgang Sundermeyer. "Darstellung perhalogenierter Mesylsulfene, X3C — SO2 — C(X) = SO2, und ihre Stabilisierung durch Chinuclidin / Preparation of Perhalogenated Mesylsulfenes, X3C —SO2— C(X) = SO2, and their Stabilization with Chinuclidin." Zeitschrift für Naturforschung B 45, no. 8 (1990): 1187–92. http://dx.doi.org/10.1515/znb-1990-0813.

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Perhalogeno disulfenes (dimeric thione-S,S-dioxides) (2 a, b) are singly cleaved by TAS–fluoride forming the intermediate salts 3a and 3b. From both anions a fluoride ion can be abstracted by silicon tetrafluoride and the perhalogenated mesylsulfenes X3C — SO2— C(X)= SO2 (4 a) (X = Cl) and (4b) (X = Br) could be obtained, which are stabilized by S-coordinated quinuclidine. Hydrolysis occurs to 4 a, b forming the sulfonium salts 7a, b, which are the structural isomers to the sulfonium salts 5 a, b achieved from direct hydrolysis of 2 a, b in the presence of quinuclidine.

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16

Kumar, Nag S., and B. Mario Pinto. "Synthesis of a Sulfonium Ion Analogue of the Glycosidase Inhibitor Swainsonine." Journal of Organic Chemistry 71, no. 3 (2006): 1262–64. http://dx.doi.org/10.1021/jo052111s.

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17

Mohan, Sankar, and B. Mario Pinto. "Sulfonium-ion glycosidase inhibitors isolated from Salacia species used in traditional medicine, and related compounds." Collection of Czechoslovak Chemical Communications 74, no. 7-8 (2009): 1117–36. http://dx.doi.org/10.1135/cccc2009024.

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A novel class of naturally-occurring glycosidase inhibitors, having sulfonium sulfate structures, has been isolated as bioactive components from Indian plants, belonging to the Salacia genus in the family Celastraceae, and used in Ayurvedic medicine for the treatment of type-2 diabetes. Thus far, five such sulfonium salts, namely, salacinol, kotalanol, salaprinol, ponkoranol and de-O-sulfonated kotalanol, have been isolated from this plant species. These structurally unique zwitterionic glycosidase inhibitors have received much attention due to their therapeutic potential in the treatment of t

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18

Tilley, RI. "Stability Constants of Silver(I) Complexes of Bis(2-chloroethyl) Sulfide (Sulfur Mustard) and Some Related Thioethers in Polar Organic Solvents." Australian Journal of Chemistry 43, no. 9 (1990): 1573. http://dx.doi.org/10.1071/ch9901573.

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Stability constants of complexes formed between silver(I) and diethyl sulfide, 2-chloroethyl ethyl sulfide and bis (2-chloroethyl) sulfide (sulfur mustard) in acetone, methanol, dimethylformamide and dimethyl sulfoxide have been determined. The reduced stability of silver(I) complexes with ligands containing a 2-chloroethyl group has been explained in terms of the sulfonium ion character of the ligands.

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19

Puzzarini, Cristina. "Ab initio anharmonic force field and equilibrium structure of the sulfonium ion." Journal of Molecular Spectroscopy 242, no. 1 (2007): 70–75. http://dx.doi.org/10.1016/j.jms.2007.02.011.

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20

Valenzuela, Francisco A., Thomas K. Green, and Darwin B. Dahl. "Synthesis and Separation of a Diastereomeric Sulfonium Ion by Capillary Zone Electrophoresis." Journal of Chemical Education 75, no. 12 (1998): 1590. http://dx.doi.org/10.1021/ed075p1590.

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21

HARVEY, J. N., and H. G. VIEHE. "ChemInform Abstract: 3-Thio-Claisen Rearrangement of the Allyl Vinyl Sulfonium Ion." ChemInform 27, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199613097.

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22

Oehlschlager, Allan C., Shankar M. Singh, and Sunaina Sharma. "Squalene synthetase inhibitors: synthesis of sulfonium ion mimics of the carbocationic intermediates." Journal of Organic Chemistry 56, no. 12 (1991): 3856–61. http://dx.doi.org/10.1021/jo00012a016.

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23

Muthupradeepa, R., M. Sivakumar, R. Subadevi, and V. Suryanarayanan. "Sulfonium cation based ionic liquid incorporated polymer electrolyte for lithium ion battery." Polymer Bulletin 74, no. 5 (2016): 1677–91. http://dx.doi.org/10.1007/s00289-016-1796-y.

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24

Bagri, Priyanka, Karishma Chester, Washim Khan та Sayeed Ahmad. "Aspects of extraction and biological evaluation of naturally occurring sugar-mimicking sulfonium-ion and their synthetic analogues as potent α-glucosidase inhibitors from Salacia: a review". RSC Advances 7, № 45 (2017): 28152–85. http://dx.doi.org/10.1039/c7ra02955a.

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A review of the selective inhibitory activities of sulfonium compounds ofSalaciaagainst intestinal α-glucosidases, structural features important for effective inhibition and the toggling approach for controlling starch digestion and glucose release.

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25

Hemström, P., K. H. Holmgren, B. E. Hammarström, A. Larsson, and A. Östin. "Identification and toxicological evaluation of cyclic sulfonium ion degradation products of sulphur mustard." Marine Environmental Research 162 (December 2020): 105047. http://dx.doi.org/10.1016/j.marenvres.2020.105047.

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26

Xu, Mei-Li, and Wenhua Huang. "Metal-free carbon–carbon cross-couplings between the ion pairs in sulfonium tetraphenylborates." Tetrahedron Letters 55, no. 30 (2014): 4230–32. http://dx.doi.org/10.1016/j.tetlet.2014.05.102.

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27

Peschke, Bernd, Joan Gredal Bundgaard, and Jens Breinholt. "Synthesis of amino alcohols on solid support via sulfonium-ion mediated Darzens reaction." Tetrahedron Letters 42, no. 30 (2001): 5127–30. http://dx.doi.org/10.1016/s0040-4039(01)00952-2.

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28

Sierakowski, James, Mahasilu Amunugama, Kade D. Roberts, and Gavin E. Reid. "Substituent effects on the gas-phase fragmentation reactions of sulfonium ion containing peptides." Rapid Communications in Mass Spectrometry 21, no. 7 (2007): 1230–38. http://dx.doi.org/10.1002/rcm.2959.

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29

Zhou, Hongwei, Yanpeng Xing, Le Liu, and Junjie Hong. "Sulfur as a Bridge: Synthesis of Medium Rings via a Bicyclic Sulfonium Ion." Advanced Synthesis & Catalysis 353, no. 17 (2011): 3146–50. http://dx.doi.org/10.1002/adsc.201100502.

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30

Hoffman, Jerald L. "Ion chromatographic analysis of the purity and synthesis of sulfonium and selenonium ions." Journal of Chromatography A 588, no. 1-2 (1991): 211–16. http://dx.doi.org/10.1016/0021-9673(91)85025-b.

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31

Harrison, Christopher R., Jayden A. Sader, and Charles A. Lucy. "Sulfonium and phosphonium, new ion-pairing agents with unique selectivity towards polarizable anions." Journal of Chromatography A 1113, no. 1-2 (2006): 123–29. http://dx.doi.org/10.1016/j.chroma.2006.01.132.

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32

Das, Sribash, Oindrila Biswas, Nasim Akhtar, Anjali Patel, and Debasis Manna. "Multi-stimuli controlled release of a transmembrane chloride ion carrier from a sulfonium-linked procarrier." Organic & Biomolecular Chemistry 18, no. 45 (2020): 9246–52. http://dx.doi.org/10.1039/d0ob00938e.

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33

Sladek, Alexander, and Hubert Schmidbaur. "Notizen: Bridging of Trigoldsulfonium Clusters by a Silver(I) Ion." Zeitschrift für Naturforschung B 52, no. 2 (1997): 301–4. http://dx.doi.org/10.1515/znb-1997-0225.

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Abstract Treatment of tris[(triphenylphosphine)gold(I)]-sulfonium tetrafluoroborate with AgBF4 (molar ratio 2:1) in tetrahydrofuran affords a hepta-nuclear mixed-metal cluster trication {[(Ph3P)6Au6AgS2](thf)}3+ as the tetrafluoroborate salt. The crystal structure of the compound has been determined by X-ray diffraction. The silver atom is found in a bridging position between the two Au3S units with short contacts to both sulfur atoms and to three out of six gold atoms. The coordination sphere of the silver atom is complemented by a tetrahydrofuran molecule. In di(tri)chlorom ethane solution

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34

Svansson, Lars, Blair D. Johnston, Jian-Hua Gu, Brian Patrick, and B. Mario Pinto. "Synthesis and Conformational Analysis of a Sulfonium-Ion Analogue of the Glycosidase Inhibitor Castanospermine." Journal of the American Chemical Society 122, no. 44 (2000): 10769–75. http://dx.doi.org/10.1021/ja002038h.

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35

OEHLSCHLAGER, A. C., S. M. SINGH, and S. SHARMA. "ChemInform Abstract: Squalene Synthetase Inhibitors: Synthesis of Sulfonium Ion Mimics of the Carbocationic Intermediates." ChemInform 22, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199144271.

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36

Matsumoto, Kouichi, Yu Miyamoto, Kazuaki Shimada, et al. "Low temperature in situ Raman spectroscopy of an electro-generated arylbis(arylthio)sulfonium ion." Chemical Communications 51, no. 66 (2015): 13106–9. http://dx.doi.org/10.1039/c5cc03585f.

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37

Xing, Linlin, Qun Niu, and Chunbao Li. "Practical Glucosylations and Mannosylations Using Anomeric Benzoyloxy as a Leaving Group Activated by Sulfonium Ion." ACS Omega 2, no. 7 (2017): 3698–709. http://dx.doi.org/10.1021/acsomega.7b00729.

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38

Zhou, Hongwei, Yanpeng Xing, Le Liu, and Junjie Hong. "ChemInform Abstract: Sulfur as a Bridge: Synthesis of Medium Rings via a Bicyclic Sulfonium Ion." ChemInform 43, no. 18 (2012): no. http://dx.doi.org/10.1002/chin.201218198.

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39

Xu, Mei-Li, and Wenhua Huang. "ChemInform Abstract: Metal-Free Carbon-Carbon Cross-Couplings Between the Ion Pairs in Sulfonium Tetraphenylborates." ChemInform 45, no. 52 (2014): no. http://dx.doi.org/10.1002/chin.201452043.

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40

Novak, Bruce M., Edward Hagen, Susan Hoff, and Anand Viswanathan. "Synthesis and Photochemistry of Sulfonium Ion Polymers. Arylated and Alkylated Poly(p-phenylene sulfide) Derivatives." Macromolecules 27, no. 7 (1994): 1985–86. http://dx.doi.org/10.1021/ma00085a054.

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41

Mohan, Sankar, Sarah McAtamney, Kumarasamy Jayakanthan, Razieh Eskandari, Mark von Itzstein, and B. Mario Pinto. "Antiviral activities of sulfonium-ion glucosidase inhibitors and 5-thiomannosylamine disaccharide derivatives against dengue virus." International Journal of Antimicrobial Agents 40, no. 3 (2012): 273–76. http://dx.doi.org/10.1016/j.ijantimicag.2012.05.002.

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42

Mohan, Sankar, Razieh Eskandari, and B. Mario Pinto. "Naturally Occurring Sulfonium-Ion Glucosidase Inhibitors and Their Derivatives: A Promising Class of Potential Antidiabetic Agents." Accounts of Chemical Research 47, no. 1 (2013): 211–25. http://dx.doi.org/10.1021/ar400132g.

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43

Tinti, Francesca, Luca Bizzocchi, Claudio Degli Esposti, and Luca Dore. "Millimeter-wave spectroscopy of and its symmetric isotopologues: Determination of the molecular structure of the sulfonium ion." Journal of Molecular Spectroscopy 240, no. 2 (2006): 202–9. http://dx.doi.org/10.1016/j.jms.2006.09.009.

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44

Groenewold, Gary S., Jani C. Ingram, Anthony D. Appelhans, James E. Delmore, and David A. Dahl. "Detection of 2-chloroethyl ethyl sulfide and sulfonium ion degradation products on environmental surfaces using static SIMS." Environmental Science & Technology 29, no. 8 (1995): 2107–11. http://dx.doi.org/10.1021/es00008a033.

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45

Amunugama, Mahasilu, Kade D. Roberts, and Gavin E. Reid. "Mechanisms for the selective gas-phase fragmentation reactions of methionine side chain fixed charge sulfonium ion containing peptides." Journal of the American Society for Mass Spectrometry 17, no. 12 (2006): 1631–42. http://dx.doi.org/10.1016/j.jasms.2006.07.013.

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46

Johnson, Margaret A., Morten T. Jensen, Birte Svensson, and B. Mario Pinto. "Selection of a High-Energy Bioactive Conformation of a Sulfonium-Ion Glycosidase Inhibitor by the Enzyme Glucoamylase G2." Journal of the American Chemical Society 125, no. 19 (2003): 5663–70. http://dx.doi.org/10.1021/ja0212617.

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47

Carrithers, Stephen L., and Jerald L. Hoffman. "Sequential methylation of 2-mercaptoethanol to the dimethyl sulfonium ion, 2-(dimethylthio)ethanol, in vivo and in vitro." Biochemical Pharmacology 48, no. 5 (1994): 1017–24. http://dx.doi.org/10.1016/0006-2952(94)90373-5.

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48

Angus, PM, BT Golding, SS Jurisson, AM Sargeson, and AC Willis. "Intramolecular Condensation Reactions of S-Methylmethionine Coordinated to Cobalt(III)." Australian Journal of Chemistry 47, no. 3 (1994): 501. http://dx.doi.org/10.1071/ch9940501.

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The sulfonium salt [(en)2CoO2CCH(NH2)(CH2)2S(CH3)2]3+ (en = ethane-1,2-diamine), prepared by methylation of the thioether group of N,O-coordinated methionine , undergoes a set of complex, intramolecular condensations, oxidations, and rearrangements in aqueous base to give a novel pentadentate cobalt(III) complex (c. 20%) of the 1,9-diamino-4-hydroxy-3,7-diazanonane-4-carboxylate ion ( dhnc ). Its structure has been determined by X-ray crystallographic analysis as trans(O,O)-[Co( dhnc )(OH2)](ClO4)2.2H2O. The crystals were monoclinic, space group P 21/c with a 9.053(2), b 29.437(7), c 7.661(1)

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49

Bogdanov, Milen G., Boyan Iliev, and Willi Kantlehner. "The Residual Volume Approach II: Simple Prediction of Ionic Conductivity of Ionic Liquids." Zeitschrift für Naturforschung B 64, no. 6 (2009): 756–64. http://dx.doi.org/10.1515/znb-2009-0623.

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The Residual Volume Approach (RVA), a recently developed method for the prediction of fundamental physical properties of ionic liquids (ILs) is extended and now allows the estimation of ionic conductivity of unknown ILs, using a simple linear correlation between the ionic conductivity and previously defined substituent parameters - βx. The proposed method is applied to the conductivity correlations of 61 n-alkyl substituted imidazolium, tetraalkylammonium, pyrrolidinium, piperidinium, sulfonium and phosphonium homologous ILs, containing [BF4]−, [Tf2 N]−, [C2 F5PF]−, [CF3BF3]−, [C2H5BF3]−, [F(H

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50

Gu, Guofeng, Hui Liu та B. Mario Pinto. "Facile synthesis of sulfonium ion derivatives of 1,5-anhydro-5-thio-l-fucitol as potential α-l-fucosidase inhibitors". Carbohydrate Research 341, № 15 (2006): 2478–86. http://dx.doi.org/10.1016/j.carres.2006.08.002.

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