Stereochemistry of latilobinol
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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.
Keywords
Coumarin Nuclear Magnetic Resonance Spectrum Radius Vector Nuclear Magnetic Resonance Spectroscopy Cyclohexane RingPreview
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© Plenum Publishing Corporation 1985