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Results 1 to 25 of 62

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Synthesis of unsymmetrical disulfides with thiolsulfonates immobilised on a polystyrene supportRAJCA, A; WIESSLER, M.Tetrahedron letters. 1990, Vol 31, Num 42, pp 6075-6076, issn 0040-4039, 2 p.Article

Sensitivity of opioid receptor binding to N-substituted maleimides and methanethiosulfonate derivativesSHAHRESTANIFAR, M. S; HOWELLS, R. D.Neurochemical research. 1996, Vol 21, Num 11, pp 1295-1299, issn 0364-3190Article

A New Synthesis of Cytotoxic Thiosulfonates and the First Synthesis of Deuterated ThiosulfonatesFENG GAO; HUIYUAN ZHAI; MEINA JIN et al.Synthesis (Stuttgart). 2011, Num 22, pp 3635-3638, issn 0039-7881, 4 p.Article

The crystal and molecular structure of 4-methoxyphenyltellurenyl methanethiosulfonateHUSEBYE, S; MAARTMANN-MOE, K; MIKALSEN, O et al.Acta chemica scandinavica (1989). 1989, Vol 43, Num 6, pp 615-617, 3 p.Article

Sensitometric properties of elemental sulfur and of selected sulfur donors and acceptorsHELLING, J. O; HERZ, A. H.The Journal of imaging science and technology. 1995, Vol 39, Num 6, pp 524-532, issn 1062-3701Article

Reactions of 1-hydroxypyridine-2(1H)-thione with arenesulfinyl chlorides: a new route to S-aryl thiosulfonatesSAS, W.Journal of chemical research. Synopses (Print). 1993, Num 4, pp 160-161, issn 0308-2342Article

Thiosulfonic S-esters. V: Mechanistic aspects of the reaction with chlorotrimethylsilane and sodium iodideCAPUTO, R; FERRERI, C; PALUMBO, G et al.Tetrahedron (Oxford. Print). 1986, Vol 42, Num 19, pp 5377-5383, issn 0040-4020Article

Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates : disulfides and thiosulfonatesGLIDWELL, Christopher; LOW, John N; WARDELL, James L et al.Acta crystallographica. Section B, Structural science. 2000, Vol 56, Num 5, pp 893-905, issn 0108-7681Article

Altering the specificity of subtilisin Bacillus lentus through the introduction of positive charge at single amino acid sitesDAVIS, B. G; KHUMTAVEEPORN, K; BOTT, R. R et al.Bioorganic & medicinal chemistry. 1999, Vol 7, Num 11, pp 2303-2311, issn 0968-0896Article

Synthesis of (6E)-8-thia, and (14E)-13-thia-2,3-oxidosqualene : inhibitors of 2,3-oxidosqualene-lanosterol cyclaseYI FENG ZHENG; OEHLSCHLAGER, A. C; HARTMAN, P. G et al.Journal of organic chemistry. 1994, Vol 59, Num 19, pp 5803-5809, issn 0022-3263Article

Investigation of some thiosulfonate derivatives by means of chemical ionization and tandem mass spectrometryCURCURUTO, O; WINDERS, J; FRANCHI, D et al.Rapid communications in mass spectrometry. 1993, Vol 7, Num 7, pp 67-672, issn 0951-4198Conference Paper

Vibrational and NMR spectroscopic studies of a thiolsulphonate produced form the non-catalytic hydrogenation of polybutadieneEDWARDS, H. G. M; JOHNSON, A. F; LEWIS, I. R et al.Journal of molecular structure. 1992, Vol 268, Num 4, pp 363-372, issn 0022-2860Article

An interesting rearrangement of unsaturated sulphonate and thiosulphonate estersSERRA, A. C; DA SILVA CORREA, C. M. M.Tetrahedron letters. 1991, Vol 32, Num 45, pp 6653-6654, issn 0040-4039Article

Silicon in organosulphur chemistry. II: Synthesis of unsymmetrical disulphidesCAPOZZI, G; CAPPERUCCI, A; DEGL'INNOCENTI, A et al.Tetrahedron letters. 1989, Vol 30, Num 22, pp 2995-2998, issn 0040-4039Article

Nematicidal and antimicrobial constituents from Allium grayi Regel and Allium fistulosum L. var. caespitosumTADA, M; HIROE, Y; KIYOHARA, S et al.Agricultural and biological chemistry. 1988, Vol 52, Num 9, pp 2383-2385, issn 0002-1369Article

Sulfinic acids and related compounds. XIX: Synthesis and properties of 1-propane, 1-butane, and 1-pentanesulfinates terminally substituted with di- and trisulfide functionsMACKE, J. D; FIELD, L.Journal of organic chemistry. 1988, Vol 53, Num 2, pp 396-402, issn 0022-3263Article

Cyclic thiosulfinates and thiosulfonates from oxidation of the 2-thiacephem ring system. Synthesis of (5R)-penems by stereospecific SO2 extrusionPERRONE, E; ALPEGIANI, M; BEDESCHI, A et al.Journal of organic chemistry. 1986, Vol 51, Num 18, pp 3413-3420, issn 0022-3263Article

Combining Ring-Opening Multibranching and RAFT Polymerization: Multifunctional Linear―Hyperbranched Block Copolymers via Hyperbranched Macro-Chain-Transfer AgentsNUHN, Lutz; SCHÜLL, Christoph; FREY, Holger et al.Macromolecules (Print). 2013, Vol 46, Num 6, pp 2892-2904, issn 0024-9297, 13 p.Article

Synthesis of sulfonyl chlorides and thiosulfonates from H2O2-TiCl4BAHRAMI, Kiumars; KHODAEI, Mohammad M; KHALEDIAN, Donya et al.Tetrahedron letters. 2012, Vol 53, Num 3, issn 0040-4039, 264, 354-358 [6 p.]Article

Oxidation of disulfides with SelectfluorTM: concise syntheses of thiosulfonates and sulfonyl fluoridesKIRIHARA, Masayuki; NAITO, Sayuri; ISHIZUKA, Yuki et al.Tetrahedron letters. 2011, Vol 52, Num 24, issn 0040-4039, 3058, 3086-3089 [5 p.]Article

A Method for Obtaining Defined End Groups of Polymethacrylates Prepared by the RAFT Process during AminolysisROTH, Peter J; KESSLER, Daniel; ZENTEL, Rudolf et al.Macromolecules (Print). 2008, Vol 41, Num 22, pp 8316-8319, issn 0024-9297, 4 p.Article

Controlled site-selective protein glycosylation for precise glycan structure-catalytic activity relationshipsDAVIS, B. G; LLOYD, R. C; JONES, J. B et al.Bioorganic & medicinal chemistry. 2000, Vol 8, Num 7, pp 1527-1535, issn 0968-0896Article

A study of chain transfer to asymmetric thiolsulfonates in methyl methacrylate polymerizationVOLOSHINETS, V. A; MARINTSOVA, N. G; BILOZOR, T. K et al.Polymer science. Series B. 1998, Vol 40, Num 11-12, pp 373-377, issn 1560-0904Article

Suppressing effects of S-methyl methanethiosulfonate and diphenyl disulfide on mitomycin C-induced somatic mutation and recombination in Drosophila melanogaster and micronuclei in miceNAKAMURA, Y. K; KAWAI, K; FURUKAWA, H et al.Mutation research. DNA repair. 1997, Vol 385, Num 1, pp 41-46, issn 0921-8777Article

Chemoprevention of azoxymethane-induced colon carcinogenesis by dietary feeding of S-methyl methane thiosulfonate in male F344 ratsKAWAMORI, T; TANAKA, T; OHNISHI, M et al.Cancer research (Baltimore). 1995, Vol 55, Num 18, pp 4053-4058, issn 0008-5472Article

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