## Abstract The ^1^H and ^13^C 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 ^1^H, ^13^C, DEPT and HMQC and also 1D NOE difference spectroscopy. Copyri
1H and 13C NMR signal assignment of synthetic (-)-methyl thyrsiflorin B acetate, (-)-thyrsiflorin C and several scopadulane derivatives
✍ Scribed by Miguel A. González; Ramón J. Zaragozá
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 112 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1629
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✦ Synopsis
The 1 H and 13 C NMR signal assignment of the data of 13 scopadulane-type diterpenes is reported. It was based on one-and two-dimensional NMR techniques which included 1 H, 13 C, DEPT, HMQC and 1D NOE difference spectroscopy.
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