## Abstract The ^13^C NMR spectra of several diterpenic derivatives having the podocarpane and cassane skeleton were recorded and interpreted. The most significant effects due to substituent orientation, B/C ring junction stereochemistry and conformational changes are briefly discussed.
13C NMR spectra of cassane diterpenoids. The stereochemistry of the caesalpins
✍ Scribed by J. D. Connolly; Fulvia Orsini; Francesca Pelizzoni; Giuliana Ricca
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 224 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Assignments of the ^13^C NMR resonances for some cassane diterpenoids have been made. The data have proved to be a useful tool for the stereochemical examination of the caesalpins.
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