2000
DOI: 10.1021/np990470a
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New Xenicane Diterpenes Isolated from the Acetone Extract of the Soft Coral Xenia florida

Abstract: Six new xenicane diterpenes have been isolated from the acetone extract of the soft coral Xenia florida. Two of them are diterpenes containing a bicyclic [4.3.1] ring system. Three of them seem to be precursors for diterpenes possessing the bicyclic [4.3.1] ring system. One is a common monocarbocyclic diterpene with a cyclononane skeleton.

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Cited by 25 publications
(38 citation statements)
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“…1,2 These corals have been widely studied as they afford a huge number of terpenes with unique structural features and biological activity. [3][4][5][6][7] Xenia (Xeniidae) commonly occurs in clear water of the tropics in the form of small yellowish cylindrical or clavate colonies. 8 The genus has proved to be a rich source of diterpenoids containing a 9-membered monocarbocyclic ring (xenicanes) 6 as well as sesquiterpenes with cadinene skeletons.…”
Section: Introductionmentioning
confidence: 99%
“…1,2 These corals have been widely studied as they afford a huge number of terpenes with unique structural features and biological activity. [3][4][5][6][7] Xenia (Xeniidae) commonly occurs in clear water of the tropics in the form of small yellowish cylindrical or clavate colonies. 8 The genus has proved to be a rich source of diterpenoids containing a 9-membered monocarbocyclic ring (xenicanes) 6 as well as sesquiterpenes with cadinene skeletons.…”
Section: Introductionmentioning
confidence: 99%
“…The 13 C NMR and HMBC data indicated two carbonyl signals: one belonged to the acetate group [δ 170.3] attached to C-3, and the other one was the carbonyl [δ 172.30, C-1] of the methyl ester moiety. The NMR data of 4 were also compared to those of xenibecin, 15 florlide F, 16 and 9-deoxyisoxeniolide-A, 17 which led to the conclusion that the structure of 4 is analogous to florlide F, 16 with the only difference in the ring system, in which one double bond appears between C-7 and C-8, similar to that found in the ring system of xenibecin and 9-deoxyisoxeniolide-A. The relative configuration at C-4a and C-11a was deduced by ROESY analysis.…”
Section: Resultsmentioning
confidence: 99%
“…In 1998, seven new diterpenoids, florlides A-E (26-30) and florethers A and B (31 and 32), were isolated from X. florida collected at Bonotsu, Kagoshima Prefecture, Japan [33]. In 2000, six new diterpenoids, namely 11-O-methylflorlide A (33), 2β-epoxyfloridicin (34), xeniafaraunol B (35), and florlides F-H (36)(37)(38), were isolated from X. florida collected at Bonotsu, Kagoshima Prefecture, Japan [34]. In 2005, three new diterpenoids, xeniolactones A-C (39-41), were isolated from X. florida collected at Green Island, off Taiwan [35].…”
Section: Xenia Floridamentioning
confidence: 99%