2-Fluoroethanol (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "2-Fluoroethanol" in English language version.

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contaminantdb.ca

dguv.de

gestis.dguv.de

doi.org

  • Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2000). "Fluorine Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a11_349. ISBN 3527306730.
  • Hoffmann, Friedrich W. (1948). "Preparation of Aliphatic Fluorides". Journal of the American Chemical Society. 70 (7): 2596–2597. doi:10.1021/ja01187a505. PMID 18875124.
  • Shahak, Israel; Bergmann, Ernst D. (1965). "A convenient of synthesis β- and γ-fluoro-alcohols". Chem. Commun. (7): 122a. doi:10.1039/c1965000122a.
  • Bhadury, Pinaki S.; Raza, Syed K.; Jaiswal, Devendra K. (1999). "A semi-molten mixture of hexadecyltributylphosphonium bromide and potassium fluoride in the synthesis of organofluorine compounds". Journal of Fluorine Chemistry. 99 (2): 115–117. Bibcode:1999JFluC..99..115B. doi:10.1016/s0022-1139(99)00121-9.
  • Huang, Jinfan; Hedberg, Kenneth (1989). "Conformational analysis. 13. 2-Fluoroethanol. An investigation of the molecular structure and conformational composition at 20, 156, and 240.degree.. Estimate of the anti-gauche energy difference". Journal of the American Chemical Society. 111 (18): 6909–6913. doi:10.1021/ja00200a003.
  • Dixon, David A.; Smart, Bruce E. (1991). "Conformational energies of 2-fluoroethanol and 2-fluoroacetaldehyde enol: Strength of the internal hydrogen bond". The Journal of Physical Chemistry. 95 (4): 1609–1612. doi:10.1021/j100157a020.
  • Bronnert, D.L.E.; Saunders, B.C. (1960). "Toxic fluorine compounds containing the C—F link—XI". Tetrahedron. 10 (3–4): 160–163. doi:10.1016/s0040-4020(01)97802-0.
  • Falzon, C. L., Ackermann, U., Spratt, N., Tochon-Danguy, H. J., White, J., Howells, D., & Scott, A. M. (2006).F-18 labelledN,N-bis-haloethylamino-phenylsulfoxides — a new class of compounds for the imaging of hypoxic tissue. Journal of Labelled Compounds and Radiopharmaceuticals, 49(12), 1089–1103. https://doi.org/10.1002/jlcr.1129
  • Pan, J., Pourghiasian, M., Hundal, N., Lau, J., Bénard, F., Dedhar, S., & Lin, K.-S. (2013). 2-[18F]-fluoroethanol and 3-[18F]-fluoropropanol: facile preparation, biodistribution in mice, and their application as nucleophiles in the synthesis of [18F]fluoroalkyl aryl ester and ether PET tracers. Nuclear Medicine and Biology, 40(6), 850–857. https://doi.org/10.1016/j.nucmedbio.2013.04.009
  • Treble D. H. (1962). The metabolism of 2-fluoroethanol. The Biochemical journal, 82(1), 129–134. https://doi.org/10.1042/bj0820129
  • Goncharov, N. V., Jenkins, R. O., & Radilov, A. S. (2006). Toxicology of fluoroacetate: a review, with possible directions for therapy research. Journal of applied toxicology : JAT, 26(2), 148–161. https://doi.org/10.1002/jat.1118

harvard.edu

ui.adsabs.harvard.edu

  • Bhadury, Pinaki S.; Raza, Syed K.; Jaiswal, Devendra K. (1999). "A semi-molten mixture of hexadecyltributylphosphonium bromide and potassium fluoride in the synthesis of organofluorine compounds". Journal of Fluorine Chemistry. 99 (2): 115–117. Bibcode:1999JFluC..99..115B. doi:10.1016/s0022-1139(99)00121-9.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Hoffmann, Friedrich W. (1948). "Preparation of Aliphatic Fluorides". Journal of the American Chemical Society. 70 (7): 2596–2597. doi:10.1021/ja01187a505. PMID 18875124.

oclc.org

pubs-rsc-org.ru.idm.oclc.org