Abstract
AbstractThe 1H and 13C NMR spectral analysis of synthetic (−)‐methylthyrsiflorin A and 10 scopadulan precursors is reported. Resonance assignments were based on one‐ and two‐dimensional NMR techniques, which included 1H, 13C, DEPT and HMQC and also 1D NOE difference spectroscopy. Copyright © 2001 John Wiley & Sons, Ltd.
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