Frémyova sůl (Czech Wikipedia)

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

refsWebsite
Global rank Czech rank
2nd place
4th place
4th place
8th place
549th place
904th place
222nd place
83rd place

doi.org

  • P. A. Wehrli; F. Pigott. Oxidation with the nitrosodisulfonate radical. I. Preparation and use of sodium nitrosodisulfonate: trimethyl-p-benzoquinone. Organic Syntheses. 1972, s. 83. doi:10.15227/orgsyn.052.0083. 
  • S. Colacicchi; V. Carnicelli; G. Gualtieri; A. Di Giulio. EPR study of Frémy's salt nitroxide reduction by ascorbic acid; influence of bulk pH values. Research on Chemical Intermediates. 2000, s. 885–896. doi:10.1163/156856700X00372. 
  • J. Zielonka; H. Zhao; Y. Xu; B. Kalyanaraman. Mechanistic similarities between oxidation of hydroethidine by Frémy's salt and superoxide: stopped-flow optical and EPR studies. Free Radical Biology & Medicine. 2005, s. 853–863. doi:10.1016/j.freeradbiomed.2005.05.001. PMID 16140206. 
  • H. Zimmer; D. C. Lankin; S. W. Horgan. Oxidations with potassium nitrosodisulfonate (Frémy's radical). Teuber reaction. Chemical Reviews. 1971, s. 229–246. doi:10.1021/cr60270a005. 
  • I. Islam; E. B. Skibo; R. T. Dorr; D. S. Alberts. Structure-activity studies of antitumor agents based on pyrrolo[1,2-a]benzimidazoles: new reductive alkylating DNA cleaving agents. Journal of Medicinal Chemistry. 1991, s. 2954–2961. doi:10.1021/jm00114a00. PMID 1920349. 
  • H. J. Teuber; S. Benz. Reaktionen mit Nitrosodisulfonat, XXXVI. Chinolin-chinone-(5.6) aus 5-Hydroxy-chinolinen. Chemische Berichte. 1967, s. 2918–2929. Dostupné online. doi:10.1002/cber.19671000916. [nedostupný zdroj]
  • H. J. Teuber. Use of dipotassium nitrosodisulfonate (Frémy's salt): 4,5-dimethyl-o-benzoquinone. Organic Syntheses. 1972, s. 88. doi:10.15227/orgsyn.052.0088. 
  • W. Xue; D. Warshawsky; M. Rance; K. Jayasimhulu. A metabolic activation mechanism of 7H-dibenzo[c,g]carbozole via o-quinone. Part 1: synthesis of 7H-dibenzo[c,g]carbozole-3,4-dione and reactions with nucleophiles. Polycyclic Aromatic Compounds. 2002, s. 295–300. doi:10.1080/10406630290026957. 
  • M. Wilchek; T. Miron. Mussel-inspired new approach for polymerization and cross-linking of peptides and proteins containing tyrosines by Frémy's salt oxidation. Bioconjugate Chemistry. 2015, s. 502–510. doi:10.1021/bc5006152. PMID 25692389. 
  • G. Fichman; J. P. Schneider. Utilizing Frémy's Salt to Increase the Mechanical Rigidity of Supramolecular Peptide-Based Gel Networks. Frontiers in Bioengineering and Biotechnology. 2021. doi:10.3389/fbioe.2020.594258. PMID 33469530. 
  • Z. L. Liu; Z. X. Han; P. Chen; Y. C. Liu. Stopped-flow ESR study on the reactivity of vitamin E, vitamin C and its lipophilic derivatives towards Frémy's salt in micellar systems. Chemistry and Physics of Lipids. 1990. doi:10.1016/0009-3084(90)90090-E. PMID 1965427. 
  • Z. L. Liu; Z. X. Han; P. Chen; Y. C. Liu. Stopped-flow ESR study on the reactivity of vitamin E, vitamin C and its lipophilic derivatives towards Frémy's salt in micellar systems. Chemistry and Physics of Lipids. 1990. doi:10.1016/0009-3084(90)90090-E. PMID 1965427. 

nih.gov

ncbi.nlm.nih.gov

  • J. Zielonka; H. Zhao; Y. Xu; B. Kalyanaraman. Mechanistic similarities between oxidation of hydroethidine by Frémy's salt and superoxide: stopped-flow optical and EPR studies. Free Radical Biology & Medicine. 2005, s. 853–863. doi:10.1016/j.freeradbiomed.2005.05.001. PMID 16140206. 
  • I. Islam; E. B. Skibo; R. T. Dorr; D. S. Alberts. Structure-activity studies of antitumor agents based on pyrrolo[1,2-a]benzimidazoles: new reductive alkylating DNA cleaving agents. Journal of Medicinal Chemistry. 1991, s. 2954–2961. doi:10.1021/jm00114a00. PMID 1920349. 
  • M. Wilchek; T. Miron. Mussel-inspired new approach for polymerization and cross-linking of peptides and proteins containing tyrosines by Frémy's salt oxidation. Bioconjugate Chemistry. 2015, s. 502–510. doi:10.1021/bc5006152. PMID 25692389. 
  • G. Fichman; J. P. Schneider. Utilizing Frémy's Salt to Increase the Mechanical Rigidity of Supramolecular Peptide-Based Gel Networks. Frontiers in Bioengineering and Biotechnology. 2021. doi:10.3389/fbioe.2020.594258. PMID 33469530. 
  • Z. L. Liu; Z. X. Han; P. Chen; Y. C. Liu. Stopped-flow ESR study on the reactivity of vitamin E, vitamin C and its lipophilic derivatives towards Frémy's salt in micellar systems. Chemistry and Physics of Lipids. 1990. doi:10.1016/0009-3084(90)90090-E. PMID 1965427. 
  • Z. L. Liu; Z. X. Han; P. Chen; Y. C. Liu. Stopped-flow ESR study on the reactivity of vitamin E, vitamin C and its lipophilic derivatives towards Frémy's salt in micellar systems. Chemistry and Physics of Lipids. 1990. doi:10.1016/0009-3084(90)90090-E. PMID 1965427. 

pubchem.ncbi.nlm.nih.gov

tripod.com

chemistris.tripod.com

  • Synthesis and Characterization of Potassium Nitrosodisulfonate, Frémy's Salt [online]. Dostupné online. 

wiley.com

www3.interscience.wiley.com