## Abstract Three prenylflavanones, sigmoidins A, B and C, were studied using one‐ and two‐dimensional NMR techniques. The interpretation of these spectra led to the definitive assignments of all carbon and hydrogen chemical shifts.
Assignment of the 1H and 13C NMR spectra of the C21 steroids 12-β-O-acetyltenacigenin A and tenacigenin A by two-dimensional NMR techniques and computer modeling
✍ Scribed by Si-Qi Luo; Long-Ze Lin; Geoffrey A. Cordell; Liang Xue; Michael E. Johnson
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 592 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Stereochemical assignments of the C~21~ steroids 12‐β‐O‐acetyltenacigenin A and tenacigenin A were performed by use of two‐dimensional phase‐sensitive COSY, ROESY, ^1^H and ^13^C shift correlation spectroscopy (HETCOR and FLOCK), and ambiguous assignments were resolved through molecular modeling comparisons. This combination of techniques is applicable for the assignment of the highly overlapped ^1^H signals of these steroids.
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