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Gersolide, a diterpenoid with a new rearranged carbon skeleton from the soft coral Gersemia rubiformis
β Scribed by David E. Williams; Raymond J. Andersen; Laszlo Parkanyi; Jon Clardy
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 151 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The structure of gersolide (4), a diterpenoid isolated from extracts of the soft coral Gersemia rubiformis, has been solved via single crystal x-ray diffraction analysis.
Soft corals are the richest marine source of diterpenoids.
Many laboratories are finding functional group variants of well-known structures as well as new carbon skeletons.'
We recently
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## Structures of stolonidiol (1) and stolonidiol monoacetate (z), new marine diterpenoids with a strong cytotoxic activity from the Japanese soft coral Clavularia sp., were established by -means of spectroscopic analyses, chemical reactions, and X-ray crystallographic analysis.