Fenol (Slovenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fenol" in Slovenian language version.

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bruichladdich.com

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chemguide.co.uk

doi.org

  • »Front Matter«. Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. str. 690. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. Only one name is retained, phenol, for C6H5-OH, both as a preferred name and for general nomenclature.

essentialchemicalindustry.org

fordham.edu

legacy.fordham.edu

google.si

books.google.si

harvard.edu

isites.harvard.edu

holocaust-history.org

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itrust.de

gestis.itrust.de

iupac.org

goldbook.iupac.org

  • Alcohols. IUPAC, Compendium of Chemical Terminology. 2. izdaja. 1997.
  • Phenols. IUPAC, Compendium of Chemical Terminology. 2. izdaja. 1997.

mcgroup.co.uk

nih.gov

ncbi.nlm.nih.gov

  • A. Kütt, V. Movchun, T. Rodima, T. Dansauer, E.B. Rusanov, I. Leito, I. Kaljurand, J. Koppel, V. Pihl, I. Koppel, G. Ovsjannikov, L. Toom, M. Mishima, M. Medebielle, E. Lork, G.V. Röschenthaler, I.A. Koppel, A.A. Kolomeitsev (2008). Pentakis(trifluoromethyl)phenyl, a Sterically Crowded and Electron-withdrawing Group: Synthesis and Acidity of Pentakis(trifluoromethyl)benzene, -toluene, -phenol, and -aniline. The Journal of Organic Chemistry 73 (7): 2607–20. doi: 10.1021/jo702513w. PMID 18324831.
  • P.J. Silva (2009). Inductive and Resonance Effects on the Acidities of Phenol, Enols, and Carbonyl α-Hydrogens. J. Org. Chem. 74 (2): 914–916. doi: 10.1021/jo8018736. PMID 19053615.
  • P. Juteau, V. Côté, M.F. Duckett, R. Beaudet, F. Lépine, R. Villemur, J.G. Bisaillon (2005). Cryptanaerobacter phenolicus gen. nov., sp. nov., an anaerobe that transforms phenol into benzoate via 4-hydroxybenzoate. International Journal of Systematic and Evolutionary Microbiology 55 (1): 245–50. doi: 10.1099/ijs.0.02914-0. PMID 15653882.
  • M. Rehfuss, J. Urban (2005). Rhodococcus phenolicus sp. nov., a novel bioprocessor isolated actinomycete with the ability to degrade chlorobenzene, dichlorobenzene and phenol as sole carbon sources. Systematic and Applied Microbiology 28 (8): 695–701. doi: 10.1016/j.syapm.2005.05.011. PMID 16261859.
  • T.M. Lin, S.S. Lee, C.S. Lai, S.D. Lin (junij 2006). Phenol burn. Burns: Journal of the International Society for Burn Injuries 32(4): 517–21. doi: 10.1016/j.burns.2005.12.016. PMID 16621299.
  • M.A. Warner, J.V. Harper (1985). Cardiac dysrhythmias associated with chemical peeling with phenol. Anesthesiology 62 (3): 366–7. doi: 10.1097/00000542-198503000-00030. PMID 2579602.
  • C. Hanscha, S.C. McKarns, C.J. Smith, D.J. Doolittle (junij 2000). Comparative QSAR evidence for a free-radical mechanism of phenol-induced toxicity. Chemico-Biological Interactions 127 (1): 61–72. doi: 10.1016/S0009-2797(00)00171-X. PMID 10903419.
  • V.K.H. Brown, V.L. Box, B.J. Simpson (1975). Decontamination procedures for skin exposed to phenolic substances. Archives of Environmental Health 30 (1): 1–6. doi: 10.1080/00039896.1975.10666623. PMID 1109265.
  • T.G. Pullin, M.N. Pinkerton, R.V. Johnston, D.J. Kilian (1978). Decontamination of the skin of swine following phenol exposure: a comparison of the relative efficacy of water versus polyethylene glycol/industrial methylated spirits. Toxicol Appl Pharmacol 43 (1): 199–206. doi: 10.1016/S0041-008X(78)80044-1. PMID 625760.

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