Theoretical and Experimental Chemistry

, Volume 14, Issue 4, pp 441–443 | Cite as

An NMR study of the diastereotopic nature of fluorine atoms and protons using Eu(fod)3

  • T. Ya. Lavrenyuk
  • Yu. P. Egorov
  • E. A. Pomanenko
  • V. A. Shokol
  • Yu. A. Paliichuk
Brief Communications
  • 27 Downloads

Keywords

Fluorine Fluorine Atom 

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Literature cited

  1. 1.
    E. V. Konovalov, T. Ya. Lavrenyuk, and E. P. Saenko, “A 19F NMR study of the diastereotopic nature of trifluoromethyl groups in cyclohexane derivatives using a shift reagent,” Teor. Eksp. Khim., 10, No. 5, 687–690 (1974).Google Scholar
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    E. V. Konovalov, T. Ya. Lavrenyuk, Yu. P. Egorov, S. N. Gaidamaka, and A. M. Aleksandrov, “An NMR study of compounds containing asymmetric phosphorus and sulfur atoms using Eu(fod)3” Teor. Eksp. Khim., 13, No. 3, 407–410 (1977).Google Scholar
  3. 3.
    G. E. Wright, “NMR assignment of diastereotopic protons in amphetamine by the use of Eu(fod)3,” Tetrahedron Lett., No. 13, 1097–1098 (1973).Google Scholar
  4. 4.
    B. Östman, “Investigations of dithienylglycolic esters. IV. Solvent effects on the chemical shift differences of the diastereotopic thienyl protons in an asymmetric 2,2′-di-thienylglycolic ester,” Tetrahedron, 29, No. 11, 2115–2118 (1973).Google Scholar
  5. 5.
    H. S. Gutowsky, “Nuclear magnetic resonance (N.M.R.) splittings due to molecular asymmetry,” J. Chem. Phys., 37, 2196–2197 (1962).Google Scholar

Copyright information

© Plenum Publishing Corporation 1979

Authors and Affiliations

  • T. Ya. Lavrenyuk
    • 1
  • Yu. P. Egorov
    • 1
  • E. A. Pomanenko
    • 1
  • V. A. Shokol
    • 1
  • Yu. A. Paliichuk
    • 1
  1. 1.Institute of Organic ChemistryAcademy of Sciences of the Ukrainian SSRKiev

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