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Journal of Applied Spectroscopy

, Volume 78, Issue 2, pp 189–196 | Cite as

NMR spectra of 3β-hydroxy-5α-cholane derivatives, zymosterol synthesis intermediates

  • A. V. Baranovsky
  • A. A. Bolotin
  • V. P. Kiselev
Article
  • 46 Downloads

Proton and carbon resonances in NMR spectra of a number of derivatives of 3β-hydroxy-5α-cholanes, zymosterol synthesis intermediates, have been completely assigned using 2D NMR spectroscopy methods. The stereochemistry of the chiral centers and the structures of the molecules have been confirmed.

Keywords

steroids hydroboration epoxide NMR spectroscopy stereochemistry nuclear Overhauser effect 

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Copyright information

© Springer Science+Business Media, Inc. 2011

Authors and Affiliations

  • A. V. Baranovsky
    • 1
  • A. A. Bolotin
    • 1
  • V. P. Kiselev
    • 1
  1. 1.Institute of Bioorganic ChemistryNational Academy of Sciences of BelarusMinskBelarus

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