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Thiosulfináty (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Thiosulfináty" in Czech language version.

refsWebsite
Global rank Czech rank
20doi.org
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3nih.gov
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2web.archive.org
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doi.org

  • J. L. Kice. Mechanisms and reactivity in reactions of organic oxyacids of sulfur and their anhydrides. Advances in Physical Organic Chemistry. 1980, s. 65–181. doi:10.1016/S0065-3160(08)60128-8. 
  • T. Takata; T. Endo. Thiosulphinic acids and esters. The Chemistry of Sulphinic Acids, Esters and Their Derivatives, S. Patai, Ed.. 1990, s. 527–575. doi:10.1002/9780470772270.ch18. 
  • S. Braverman; M. Cherkinsky; S. Levinger. Alkanethiosulfinic Acid Esters. Sci. Synth.. 2007, s. 229–235. doi:10.1002/9780470772270.ch18. 
  • R. Kubec; R. B. Endo; A. J. Dane; R. A. Musah; J. Schraml; A. Vattekkatte; E. Block. Applications of DART Mass Spectrometry in Allium Chemistry. (Z)-Butanethial S-Oxide and 1-Butenyl Thiosulfinates and their S-(E)-1-Butenylcysteine S-Oxide Precursor from Allium siculum. Journal of Agricultural and Food Chemistry. 2010, s. 1121–1128. doi:10.1021/jf903733e. PMID 20047275. 
  • E. Block; A. J. Dane; S. Thomas; R. B. Cody. Applications of Direct Analysis in Real Time–Mass Spectrometry (DART-MS) in Allium Chemistry. 2-Propenesulfenic and 2-Propenesulfinic Acids, Diallyl Trisulfane S-Oxide and Other Reactive Sulfur Compounds from Crushed Garlic and Other Alliums. Journal of Agricultural and Food Chemistry. 2010, s. 4617–4625. doi:10.1021/jf1000106. PMID 20225897. 
  • R. Kubec; S. Kim; R. A. Musah. S-Substituted cysteine derivatives and thiosulfinate formation in Petiveria alliacea--Part II. Phytochemistry. 2002, s. 675–680. Dostupné v archivu pořízeném dne 2016-03-03. doi:10.1016/S0031-9422(02)00328-X.  Archivováno 3. 3. 2016 na Wayback Machine.
  • Allelochemicals of the tropical weed Sphenoclea zeylanica. Phytochemistry. 2000, s. 131–140. doi:10.1016/S0031-9422(00)00264-8. 
  • H. Yanagawa; T. Kato; Y. Kitahara. Asparagusic acid-S-oxides, new plant growth regulators in etiolated young asparagus shoots. Tetrahedron Letters. 1973, s. 1073–1075. doi:10.1016/S0040-4039(01)95907-6. 
  • T. Kato; M. Numata. Brugierol and isobrugierol, trans- and cis-1,2-dithiolane-1-oxide, from Brugiera conjugata. Tetrahedron Letters. 1972, s. 203–206. doi:10.1016/S0040-4039(01)84280-5. 
  • L. D. Small; J. H. Bailey; C. J. Cavallito. Alkyl thiolsulfinates. Journal of the American Chemical Society. 1947, s. 1710–1713. doi:10.1021/ja01199a040. 
  • D. J. Weix; J. A. Ellman. (RS)-(+)-2-Methyl-2-Propanesulfinamide [tert-Butanesulfinamide]. Organic Syntheses. 2005, s. 157. doi:10.1021/ja01199a040. 
  • E. Block. The Chemistry of Alkyl Thiosulfinate Esters. III. tert-Butanethiosulfoxylic Acid. Journal of the American Chemical Society. 1972, s. 644–645. doi:10.1021/ja00757a060. 
  • T. L. Moore; D. E. O'Connor. The Reaction of Methanesulfenyl Chloride with Alkoxides and Alcohols. Preparation of Aliphatic Sulfenate and Sulfinate Esters. The Journal of Organic Chemistry. 1966, s. 3587–3592. doi:10.1021/jo01349a027. 
  • E. Block; J. O'Connor. The Chemistry of Alkyl Thiosulfinate Esters. VI. Preparation and Spectral Studies. Journal of the American Chemical Society. 1974, s. 3921–3929. doi:10.1021/ja00819a033. 
  • E. Block; J. O'Connor. The Chemistry of Alkyl Thiosulfinate Esters. VII. Mechanistic Studies and Synthetic Applications. Journal of the American Chemical Society. 1974, s. 3929–3944. doi:10.1021/ja00819a034. 
  • A. Ishii; T. Akazawa; M. X. Ding; T. Honjo; J. Nakayama; M. Hoshino; M. Shiro. First isolable dithiiranes: 3-(1,1,3,3-tetramethyl-4-oxo-4-phenylbutyl)-3-phenyldithiirane 1-oxides. Journal of the American Chemical Society. 1993, s. 4914–4915. doi:10.1021/ja00064a072. 
  • A. Ishii; T. Kawai; M. Noji; J. Nakayama. Synthesis and reactions of a monosubstituted dithiirane 1-oxide, 3-(9-triptycyl)dithiirane 1-oxide. Tetrahedron. 2005, s. 6693–6699. doi:10.1016/j.tet.2005.05.017. 
  • P. T. Lynett; K. Butts; V. Vaidya; G. E. Garretta; D. A. Pratt. The mechanism of radical-trapping antioxidant activity of plant-derived thiosulfinates. Organic and Biomolecular Chemistry. 2011, s. 3320–3330. doi:10.1039/c1ob05192j. 
  • S. Kim; R. Kubec; R. A. Musah. Antibacterial and antifungal activity of sulfur-containing compounds from Petiveria alliacea. Journal of Ethnopharmacology. 2006, s. 188–192. Dostupné v archivu pořízeném dne 2016-03-03. doi:10.1016/j.jep.2005.08.072. PMID 16229980.  Archivováno 3. 3. 2016 na Wayback Machine.
  • P. Koch; E. Ciuffarin; A. Fava. Thermal disproportionation of aryl arenethiolsulfinates. Kinetics and mechanism. Journal of the American Chemical Society. 1970, s. 5971–5977. doi:10.1021/ja00723a026. 

nih.gov

ncbi.nlm.nih.gov

  • R. Kubec; R. B. Endo; A. J. Dane; R. A. Musah; J. Schraml; A. Vattekkatte; E. Block. Applications of DART Mass Spectrometry in Allium Chemistry. (Z)-Butanethial S-Oxide and 1-Butenyl Thiosulfinates and their S-(E)-1-Butenylcysteine S-Oxide Precursor from Allium siculum. Journal of Agricultural and Food Chemistry. 2010, s. 1121–1128. doi:10.1021/jf903733e. PMID 20047275. 
  • E. Block; A. J. Dane; S. Thomas; R. B. Cody. Applications of Direct Analysis in Real Time–Mass Spectrometry (DART-MS) in Allium Chemistry. 2-Propenesulfenic and 2-Propenesulfinic Acids, Diallyl Trisulfane S-Oxide and Other Reactive Sulfur Compounds from Crushed Garlic and Other Alliums. Journal of Agricultural and Food Chemistry. 2010, s. 4617–4625. doi:10.1021/jf1000106. PMID 20225897. 
  • S. Kim; R. Kubec; R. A. Musah. Antibacterial and antifungal activity of sulfur-containing compounds from Petiveria alliacea. Journal of Ethnopharmacology. 2006, s. 188–192. Dostupné v archivu pořízeném dne 2016-03-03. doi:10.1016/j.jep.2005.08.072. PMID 16229980.  Archivováno 3. 3. 2016 na Wayback Machine.

web.archive.org