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.
ChemInform Abstract: First Diastereoselective Synthesis of (-)-Methyl Thyrsiflorin A, (-)-Methyl Thyrsiflorin B Acetate, and (-)-Thyrsiflorin C.
✍ Scribed by Manuel Arno; Miguel A. Gonzales; M. Luisa Marin; Ramon J. Zaragoza
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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📜 SIMILAR VOLUMES
## 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
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