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4′-Bromobutyl ent-16-oxobeyeran-19-oate
oleh: Xiaoming Zha, Junqing Chen
Format: | Article |
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Diterbitkan: | International Union of Crystallography 2010-03-01 |
Deskripsi
The title compound, C24H37BrO3, is a tetracyclic diterpenoid with a beyerane skeleton, synthesized by esterification of isosteviol. It comprises a fused four-ring system A/B/C/D. Rings A and B have a chair conformation, whereas ring C is an unsymmetrical distorted chair; the remaining five-membered ring D adopts an envelope conformation. The stereochemistry of the A/B and B/C ring junctions are trans, while the C/D junction is cis.