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Stereochemistry of latilobinol

Abstract

The results are given of a study of the stereochemistry of a coumarin terpenoid derivative — latilobinol — by nuclear magnetic resonance spectroscopy using lanthanoid shift reagents. On the basis of the results obtained, it has been established that the hydroxy group in the cyclohexane ring occupies the equatorial position.

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Literature cited

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Additional information

Leningrad Sanitary-Rygienic Medical Institute. Translated from Khimiya Prirodnykh Soedinenii, No.6, pp. 712–716, November–December, 1984.

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Abyshev, A.Z. Stereochemistry of latilobinol. Chem Nat Compd 20, 674–677 (1984). https://doi.org/10.1007/BF00580019

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Keywords

  • Coumarin
  • Nuclear Magnetic Resonance Spectrum
  • Radius Vector
  • Nuclear Magnetic Resonance Spectroscopy
  • Cyclohexane Ring