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Journal ArticleDOI

Studies of Australian soft corals. XXIII the co-occurrence of bicyclogermacrene and lemnacarnol derivatives in Parerythropodium fulvum

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TLDR
In this paper, the isolation of oxygenated bicyclogermacrenes, likely precursors of several classes of sesquiterpenes, was reported from the soft coral Parerythropodium fulvum.
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This article is published in Tetrahedron Letters.The article was published on 1980-01-01. It has received 19 citations till now.

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Nardosinanols A-I and lemnafricanol, sesquiterpenes from several soft corals, Lemnalia sp., Paralemnalia clavata, Lemnalia africana, and Rhytisma fulvum fulvum.

TL;DR: Ten new sesquiterpenes, nardosinanols A-I and lemnafricanol, have been isolated from several Kenyan soft corals, i.e., from Lemnalia sp.
Journal ArticleDOI

Marine Natural Products from Indonesian Waters

TL;DR: This review covers the literature on marine natural products discovered in Indonesian waters published from January 1970 to December 2017, and includes 732 original MNPs, 4 structures isolated for the first time but known to be synthetic entities, 34 structural revisions, 9 artifacts, and 4 proposed MNPs.
Journal ArticleDOI

Paralemnolins J-P, new sesquiterpenoids from the soft coral Paralemnalia thyrsoide

TL;DR: Six new sesquiterpenoids, paralemnolins J-O (1-6), along with one novel norsesquiter Penoids P (7), have been isolated from the soft coral Paralemnalia thyrsoides and Cytotoxicity of these metabolites toward a limited panel of cancer cell lines is described.
Journal ArticleDOI

Nardosinane sesquiterpenoids from the Formosan soft coral Lemnalia flava.

TL;DR: Four new nardosinane-type sesquiterpenoids, flavalins A-D (1-4), have been isolated from the Formosan soft coral Lemnalia flava and 1 and 2 were shown to possess significant neuroprotective activity.
Book ChapterDOI

Recent developments in the field of marine natural products with emphasis on biologically active compounds.

TL;DR: The marine flora and animal world are a rich source of biologically active compounds and among the best known of the toxic substances are tetrodotoxin, saxitoxin, and the polypeptides from sea anemones, but they will not be the main subject of this report.
References
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Gas-liquid chromatographic identification of ozonolysis fragments as a basis for micro-scale structure determinations

TL;DR: In this paper, a gas-liquid chromatographic procedure was developed for the identification of twelve molecular fragments that commonly result from microscale ozonolysis of terpenes and similar unsaturated compounds.
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