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Journal articles on the topic 'Disulone'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Begon, E., O. Chosidow, and P. Wolkenstein. "Disulone." Annales de Dermatologie et de Vénéréologie 131, no. 12 (2004): 1062–73. http://dx.doi.org/10.1016/s0151-9638(04)93842-2.

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2

Darrieux, L., H. Adamski, B. Turlin, et al. "Disulone et hépatosidérose." Annales de Dermatologie et de Vénéréologie 133, no. 8-9 (2006): 683–85. http://dx.doi.org/10.1016/s0151-9638(06)70991-7.

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3

Farhi, D., E. Bégon, P. Wolkenstein, and O. Chosidow. "Dapsone (Disulone®) en dermatologie." EMC - Dermatologie 1, no. 1 (2006): 1–11. http://dx.doi.org/10.1016/s0246-0319(05)40490-2.

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4

Farhi, D., E. Bégon, P. Wolkenstein, and O. Chosidow. "Dapsone (Disulone®) en dermatologie." EMC - Dermatologie-Cosmétologie 2, no. 2 (2005): 103–17. http://dx.doi.org/10.1016/j.emcdc.2005.06.002.

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5

Bordessoule, D., E. Liozon, M. Cransac, et al. "Effets hématologiques de la dapsone (Disulone®)." La Revue de Médecine Interne 10, no. 6 (1989): 527–30. http://dx.doi.org/10.1016/s0248-8663(89)80071-2.

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6

Daoui, L., K. Khadir, and H. Benchikhi. "Maladie de Weber Christian : efficacité de la disulone." Annales de Dermatologie et de Vénéréologie 140 (April 2013): S59. http://dx.doi.org/10.1016/j.annder.2013.01.064.

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7

Ly, K. H., E. Liozon, A. L. Fauchais, et al. "La dapsone (Disulone) dans la maladie de Horton: expérience monocentrique de 45 malades." La Revue de Médecine Interne 28 (June 2007): 59. http://dx.doi.org/10.1016/j.revmed.2007.03.082.

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8

Renoux, E., C. Gras, and P. Aubry. "Les effets secondaires de la dapsone. A propos d'un cas d'hépatite à la disulone." Médecine et Maladies Infectieuses 16, no. 8-9 (1986): 496–500. http://dx.doi.org/10.1016/s0399-077x(86)80286-4.

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9

Carassou, P., M. P. Massoure, G. Cinquetti, F. Banal, D. Andriamanantena, and B. Graffin. "C’est dans les vieilles marmites que l’on fait les meilleures soupes : à propos d’un cas de purpura thrombopénique auto-immun réfractaire, sensible à la disulone." La Revue de Médecine Interne 31 (June 2010): S107. http://dx.doi.org/10.1016/j.revmed.2010.03.141.

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10

Wong, Jessica H., Marilyn M. Olmstead, James C. Fettinger, and Jacquelyn Gervay-Hague. "A diisopropoxyphosphonate disulfone." Acta Crystallographica Section E Structure Reports Online 63, no. 6 (2007): o3046. http://dx.doi.org/10.1107/s160053680702507x.

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11

Wang, Congcong, Shi-Jun Li, Min Zhang, Donghui Wei, and Lina Ding. "Origin of stereoselectivity in an isothiourea catalyzed Michael addition reaction of aryl ester with vinyl disulfone." New Journal of Chemistry 44, no. 41 (2020): 17906–11. http://dx.doi.org/10.1039/d0nj03540h.

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12

Hahn, Josef, Petra Schmidt, Klaus Reinartz, Jörg Behrend, Gisbert Winnewisser, and Koichi M. T. Yamada. "Synthesis and Molecular Structure of Disulfane." Zeitschrift für Naturforschung B 46, no. 10 (1991): 1338–42. http://dx.doi.org/10.1515/znb-1991-1011.

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The synthesis and structure of disulfane are presented. Pure disulfane, H2S2, has been obtained by the cracking distillation of raw sulfane mixtures in a rotary evaporator, thus substituting the classical cracking column for the rotating flask of the evaporator. Pure, gaseous dideuterodisulfane could be generated by the solvolysis of bis(methyldiphenylsilyl)disulfane, (MePh2Si)2S2, with D2O in the presence of trichloroacetic acid as stabilizing agent. Partially deuterated disulfane has been prepared by H,D exchange between pure H2S2 and DCl. For the first time the molecular structure of HSSH h

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13

Zhang, Yi, Weiwei Yang, Wei Zhao, Fang Ruan, Shulei Li, and Jiping Liu. "Synthesis and characterization of SPDSCD and its flame retardant application on epoxy resins." RSC Advances 10, no. 48 (2020): 28654–63. http://dx.doi.org/10.1039/d0ra05167e.

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In this study, a flame retardant agent, 2,4,8,10-tetraoxo-3,9-diphosphospiro[5.5]undecane spirophosphate-4,4-diaminopair benzene disulfone-1,3,5-himetriazine (SPDSCD), is synthesized through a direct polycondensation reaction.

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14

Yang, Ya‐Ting, Bing‐Qin Yang, Min Li, Wei Ning, and Zhen‐Huan Lu. "Synthesis and Characterization of Tetraazaparacyclophane Disulfone." Synthetic Communications 38, no. 4 (2008): 530–36. http://dx.doi.org/10.1080/00397910701796733.

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15

Matsubara, Hiroshi, Mitsunobu Osatani, Koji Yano, Tomohiro Adachi, and Koji Yamamoto. "Synthesis and Characterisation of [2.2](5,13)Dibenzo[c;1]chrysenophane." Journal of Chemical Research 23, no. 1 (1999): 12–13. http://dx.doi.org/10.1177/174751989902300112.

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High-dilution coupling of 5,13-bis(bromomethyl)dibenzo[ c;1]chrysene (7) and 5,13-bis(sulfanylmethyl)dibenzo[ c;1]-chrysene 8 afforded the dithia derivative 9 which was converted, via the disulfone 10, into an unusually strained compound, [2.2](5,13)dibenzo[ c;1]chrysenophane 5.

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16

Chen, Hua, Jinliang Yang, Dongfang Guo, Liyuan Wang та Jun Nie. "Photopolymerization kinetics of α-disulfone cationic photoinitiator". Journal of Photochemistry and Photobiology A: Chemistry 232 (березень 2012): 57–63. http://dx.doi.org/10.1016/j.jphotochem.2012.02.005.

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17

Voronkov, M. G., L. G. Shagun, V. A. Usov, and L. E. Protasova. "2,6-Diphenyl-1,4-dithiine and its disulfone." Chemistry of Heterocyclic Compounds 23, no. 3 (1987): 355. http://dx.doi.org/10.1007/bf00762001.

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18

Ford, David K., Victor G. Young Jr, and George Barany. "Bis[(methylsulfanyl)carbonyl]disulfane." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2102. http://dx.doi.org/10.1107/s1600536812024750.

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19

Przychodzeń, Witold, Jarosław Chojnacki, and Łukasz Nierzwicki. "Medium-sized cyclic bis(anisylphosphonothioyl)disulfanes and their corresponding cyclic sulfane-structures and most characteristic reactions." New Journal of Chemistry 43, no. 38 (2019): 15413–34. http://dx.doi.org/10.1039/c9nj03682b.

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20

Goldenberg, Barbara L., Victor G. Young Jr, and George Barany. "Crystal structures of three (trichloromethyl)(carbamoyl)disulfanes." Acta Crystallographica Section E Crystallographic Communications 71, no. 10 (2015): 1169–73. http://dx.doi.org/10.1107/s2056989015015893.

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The present paper reports crystallographic studies on three related compounds that were of interest as precursors for synthetic and mechanistic work in organosulfur chemistry, as well as to model nitrogen-protecting groups: (N-methylcarbamoyl)(trichloromethyl)disulfane, C3H4Cl3NOS2, (1), (N-benzylcarbamoyl)(trichloromethyl)disulfane, C9H8Cl3NOS2, (2), and (N-methyl-N-phenylcarbamoyl)(trichloromethyl)disulfane, C9H8Cl3NOS2, (3). Their molecular structures, with similar bond lengths and angles for the CCl3SS(C=O)N moieties, are confirmed. Compounds (1) and (3) both crystallized with two independ

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21

Muthulakshmi, Selvarasu, and Doraisamyraja Kalaivani. "1,2-Bis(2,4-dinitrophenyl)disulfane." Acta Crystallographica Section E Structure Reports Online 69, no. 5 (2013): o808—o809. http://dx.doi.org/10.1107/s1600536813011082.

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22

Song, Mingzhi, and Chuangang Fan. "1,2-Bis(2-nitrophenyl)disulfane." Acta Crystallographica Section E Structure Reports Online 65, no. 11 (2009): o2835. http://dx.doi.org/10.1107/s1600536809042780.

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23

Xiao, Qi, Rui Liu, Yu-Hao Li, Hong-Bin Chen, and Hong-Jun Zhu. "1,2-Bis(4-ethynylphenyl)disulfane." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (2010): o606. http://dx.doi.org/10.1107/s1600536810004721.

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24

Watanabe, Katsuhiro, Takashi Ubukata, and Yasushi Yokoyama. "Photochromism and the fluorescence properties of bisbenzothienylethene and S,S,S′,S′-tetraoxide derivatives with dual conjugated fluorescent groups on their side chains." Photochemical & Photobiological Sciences 17, no. 6 (2018): 711–17. http://dx.doi.org/10.1039/c8pp00050f.

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25

Goethals, E., and L. Josson-Merckaert. "The Disultone of 2.2-Dihydroxymethyl-1.3-Propane Disulphonic Acid." Bulletin des Sociétés Chimiques Belges 70, no. 5-6 (2010): 218–20. http://dx.doi.org/10.1002/bscb.19610700505.

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26

Thakur, Neha, Mrituanjay D. Pandey, and Rampal Pandey. "A uniquely fabricated Cu(ii)-metallacycle as a reusable highly sensitive dual-channel and practically functional metalloreceptor for Fe3+ and Ca2+ ions: an inorganic site of cation detection." New Journal of Chemistry 42, no. 5 (2018): 3582–92. http://dx.doi.org/10.1039/c7nj03294c.

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27

Horstkotte, Burkhard, Ruth Suárez, Petr Solich, and Víctor Cerdà. "In-syringe magnetic stirring assisted dispersive liquid–liquid micro-extraction with solvent washing for fully automated determination of cationic surfactants." Anal. Methods 6, no. 24 (2014): 9601–9. http://dx.doi.org/10.1039/c4ay01695e.

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An automated simple analyzer system for the extraction of cationic surfactants as an ion-pair with disulfine blue dye is described based on the technique in-syringe magnetic stirring assisted dispersive liquid–liquid micro-extraction.

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28

Azad, Farshid Nasiri, Mehrorang Ghaedi, Arash Asfaram, et al. "Optimization of the process parameters for the adsorption of ternary dyes by Ni doped FeO(OH)-NWs–AC using response surface methodology and an artificial neural network." RSC Advances 6, no. 24 (2016): 19768–79. http://dx.doi.org/10.1039/c5ra26036a.

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The present study deals with the simultaneous removal of chrysoidine G (CG), rhodamine B (RB) and disulfine blue (DB) by Ni doped ferric oxyhydroxide FeO(OH) nanowires on activated carbon (Ni doped FeO(OH)-NWs–AC).

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29

Schroll, Alayne L., Maren Pink, and George Barany. "Bis(N-methyl-N-phenylcarbamoyl)disulfane." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (2012): o1550. http://dx.doi.org/10.1107/s1600536812016030.

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30

Prokeš, Ivan, Štefan Toma та Jean-Louis Luche. "Sonochemical preparation of aromatic α-disulfones". Tetrahedron Letters 36, № 22 (1995): 3849–50. http://dx.doi.org/10.1016/0040-4039(95)00653-t.

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31

MACK, H. G. "ChemInform Abstract: The Gas-Phase Structures of Chloro(trifluoromethyl)disulfane, CF3SSCl, and Bromo(trifluoromethyl)disulfane, CF3SSBr." ChemInform 24, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199307067.

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32

Li, Huiyi, Chaofu Tao, Ya Xie, et al. "Transformation of arylboronic acids with sodium thiosulfate into organodisulfides catalyzed by a recyclable polyoxometalate-based Cr(iii) catalyst." Green Chemistry 23, no. 16 (2021): 6059–64. http://dx.doi.org/10.1039/d1gc01415c.

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The mild and effective synthesis of symmetric and asymmetric disulfane compounds catalyzed by the polyoxometalate-based Cr(iii) catalyst [NH4]3[CrMo6O18(OH)6] is reported. The catalyst can be reused more than six times with high activity.

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33

Du, Naiying, Gilles P. Robertson, Ingo Pinnau, and Michael D. Guiver. "Polymers of Intrinsic Microporosity Derived from Novel Disulfone-Based Monomers†." Macromolecules 42, no. 16 (2009): 6023–30. http://dx.doi.org/10.1021/ma900898m.

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34

Witting, Paul K., Ben J. Wu, Mark Raftery, Peter Southwell-Keely, and Roland Stocker. "Probucol Protects against Hypochlorite-induced Endothelial Dysfunction." Journal of Biological Chemistry 280, no. 16 (2005): 15612–18. http://dx.doi.org/10.1074/jbc.m414256200.

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Atherosclerosis is associated with endothelial dysfunction and a heightened state of inflammation characterized, in part, by an increase in vascular myeloperoxidase and proteins modified by its principal oxidant, hypochlorous acid (HOCl). Here we examined whether probucol could protect against endothelial dysfunction induced by the two-electron oxidant HOCl. Hypochlorous acid eliminated endothelium-dependent relaxation of rabbit aorta, whereas endothelial function and tissue cGMP was preserved and elevated, respectively, in animals pretreated with probucol. Exogenously added probucol also prot

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35

Wang, B., E. C. Sivret, G. Parcsi, et al. "Reduced sulfur compounds in the atmosphere of sewer networks in Australia: geographic (and seasonal) variations." Water Science and Technology 69, no. 6 (2013): 1167–73. http://dx.doi.org/10.2166/wst.2013.798.

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The management of odorous emissions from sewer networks has become an important issue for sewer system operators resulting in the need to better understand the composition of reduced sulfur compounds (RSCs). Gaseous RSCs including hydrogen sulfide (H2S), methanethiol (MeSH), dimethyl sulﬁde (DMS), carbon disulﬁde (CS2), dimethyl disulﬁde (DMDS) and dimethyl trisulfide (DMTS) were measured in the atmosphere of selected sewer networks in two major Australian cities (Sydney and Melbourne) during 2011–2012. The RSC concentrations in the sewer air were detected in a highly variable range. H2S and M

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36

Mittler, P., G. Winnewisser, and K. M. T. Yamada. "Submillimeter Wave Spectrum of HS34SH." Zeitschrift für Naturforschung A 44, no. 8 (1989): 718–22. http://dx.doi.org/10.1515/zna-1989-0806.

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Abstract The rotational spectrum of 34S-substituted disulfane, HS34SH, has been measured between 60 and 420 GHz, yielding for the first time the rotational constants A = 146694.949 MHz, B = 6779.018 MHz and C = 6776.339 MHz, together with a complete set of J4 and J6 distortion constants.

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37

Liu, Dongsheng, Yaping Xu, Xinfa Li, Shaoming Ying, and Wentong Chen. "Bis(4H-1,2,4-triazol-3-yl)disulfane." Acta Crystallographica Section E Structure Reports Online 64, no. 1 (2007): o247. http://dx.doi.org/10.1107/s1600536807065452.

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38

Lamy, Thierry, Cedric Pastoret, Roch Houot, et al. "Prospective, Multicentric Phase II Randomized Trial Comparing the Efficacy of Methotrexate or Cyclophosphamide in Large Granular Lymphocytic Leukemia: A French National Study. Report on the Interim Analysis." Blood 134, Supplement_1 (2019): 1545. http://dx.doi.org/10.1182/blood-2019-123439.

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Introduction Large granular lymphocyte (LGL) leukemia is characterized by a clonal expansion of CD3+ cytotoxic T or CD3- NK cells. Prominent clinical features include neutropenia, anemia and autoimmune-associated diseases such as rheumatoid arthritis (RA). Although the disease is usually chronic and indolent, some patients may be symptomatic and require treatment. No standard therapy has been established due to the absence of prospective clinical trials. So far, low dose methotrexate, oral cyclophosphamide, and cyclosporine represent the 3 main options for initial therapy. In 2014, we launched

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39

Akhmedov, Magomed A., Shagabudin Sh Khidirov, and Madina Yu Kaparova. "ELECTROCHEMICAL OXIDATION OF DIMETHYL SULFONE IN ALKALINE MEDIUM." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 61, no. 8 (2018): 32. http://dx.doi.org/10.6060/ivkkt20186108.5707.

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In this paper the electrochemical oxidation of dimethyl sulfone (DMSO2) on a platinum electrode in an alkaline medium has been studied by cyclic voltammetry. It is shown that during the electrochemical oxidation of dimethylsulfone in an alkaline medium on a smooth platinum electrode, a significant suppression of the oxygen evolution (O2) occurs in the potential range of E = 1.3-2.0 V. By scanning electron microscopy methods, Raman scattering and infrared spectrometry it is shown that the main substance is the dimethyl disulfone (DMDSO2) during the anodic oxidation of DMSO2 on a platinum electr

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40

Kuhn, Norbert, Hans Bohnen, and Gerald Henkel. "Zur Reaktion von Carben-Addukten des Kohlenstoffdisulfids mit Brom und Iod [1] / On the Reaction of Carbene Adducts of Carbon Disulfide with Bromine and Iodine [1]." Zeitschrift für Naturforschung B 49, no. 11 (1994): 1473–80. http://dx.doi.org/10.1515/znb-1994-1105.

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AbstractThe carbene adducts 3 are obtained as stable solids from the imidazol-2-ylidenes 1 and CS2. 3 c reacts with bromine to give the cationic bromosulfane 4, whereas iodine forms the charge-transfer adduct 5. Oxidative coupling to the dicationic disulfane 6 is observed with excess of iodine. The X-ray structure analyses of 3b, 4, 5 and 6 are reported.

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41

Adam, Waldemar, Efstathios P. Gogonas та Lazaros P. Hadjiarapoglou. "Alkenyl C–H insertion of a β-disulfone iodonium ylide into flavones". Tetrahedron 59, № 40 (2003): 7929–34. http://dx.doi.org/10.1016/j.tet.2003.07.011.

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42

Xin, Wei. "1,2-Bis{2-[(4-methoxybenzylidene)amino]phenyl}disulfane." Acta Crystallographica Section E Structure Reports Online 69, no. 6 (2013): o896. http://dx.doi.org/10.1107/s1600536813011598.

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43

Frasch, Markus, and Wolfgang Sundermeyer. "Über Substitutionsreaktionen an 1,3-Dithietan-1,1,3,3-tetraoxid (Disulfen)." Chemische Berichte 126, no. 2 (1993): 537–41. http://dx.doi.org/10.1002/cber.19931260234.

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44

PROKES, I., S. TOMA та J. L. LUCHE. "ChemInform Abstract: Sonochemical Preparation of Aromatic α-Disulfones." ChemInform 26, № 37 (2010): no. http://dx.doi.org/10.1002/chin.199537127.

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45

HAHN, J., P. SCHMIDT, K. REINARTZ, J. BEHREND, G. WINNEWISSER, and K. M. T. YAMADA. "ChemInform Abstract: Synthesis and Molecular Structure of Disulfane." ChemInform 23, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.199203001.

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46

Lumbroso, H., J. M. Catel, G. Le Coustumer, and C. G. Andrieu. "A critical survey on the preferred conformations of diphenyl disulphone, dimethyl- and diphenyl-dichalcogenides, bis(3-thienyl)-disulphide and -disulphone." Journal of Molecular Structure 513, no. 1-3 (1999): 201–18. http://dx.doi.org/10.1016/s0022-2860(99)00121-0.

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47

Haenel, Matthias W., Birgit Lintner, and Dieter Schweitzer. "Transanulare Wechselwirkung bei [m.n]Phanen, 32 [1]: Modelle für Amin-Aromaten-Exciplexe: [2](1,4)Anthraceno[2](2,6)pyridinophan-1,13-dien/Transanular Interaction in [m .n]Phanes, 32 [1]: Models for Amine-Arene-Exciplexes: [2](1,4)Anthraceno[2](2,6)pyridinophan-1,13-dien." Zeitschrift für Naturforschung B 41, no. 2 (1986): 223–30. http://dx.doi.org/10.1515/znb-1986-0213.

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The [2](1,4)Anthraceno[2](2,6)pyridinophan-1,13-dien (5) and the corresponding [2.2]phane (7) were synthesized as models for exciplexes. The dithia[3.3]phanes(9) and (11) were prepared by cyclisation of the dithiols 13 and 16 with the dibromide 19. Oxidation of 9 to the disulfone 10 and vapour phase pyrolysis led to 7. Ring contraction of 9 by S-analogous Wittig ether rearrangement led to 20 which was converted to the diene 5 via oxidation to the disulfoxide 21 and pyrolytic elimination of methane sulfenic acid. Attempts to prepare 6 and 8 via similar routes from 11 failed. Electron absorption

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48

Schenzel, Alexander M., Norbert Moszner та Christopher Barner-Kowollik. "Disulfone Cross-Linkers for λ-Orthogonal Photoinduced Curing and Degradation of Polymeric Networks". ACS Macro Letters 6, № 1 (2016): 16–20. http://dx.doi.org/10.1021/acsmacrolett.6b00934.

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49

Lacour, Jérôme, David Monchaud, Gérald Bernardinelli, and France Favarger. "Synthesis, Enantiomeric Conformations, and Stereodynamics of Aromaticortho-Substituted Disulfones." Organic Letters 3, no. 9 (2001): 1407–10. http://dx.doi.org/10.1021/ol015804d.

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50

Lacour, Jérôme, David Monchaud, Jiri Mareda, France Favarger, and Gérald Bernardinelli. "Synthesis, Enantiomeric Conformations, and Stereodynamics of Aromaticortho-Substituted Disulfones." Helvetica Chimica Acta 86, no. 1 (2003): 65–81. http://dx.doi.org/10.1002/hlca.200390020.

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