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Dactylomelol, a new class of diterpene from the sea hare aplysia dactylomela

✍ Scribed by Dulce M. Estrada; José L. Ravelo; Catalina Ruiz-Pérez; Julio D. Martín; Xavier Solans

Publisher: Elsevier Science
Year: 1989
Tongue: French
Weight: 128 KB
Volume: 30
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)93347-7

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New halogenated constituents of the digestive gland of the sea hare aplysia dactylomela

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The Absolute Configurations and Biogenesis of Some New Halogenated Chamigrenes from the Sea Hare Aplysia dactylomela

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Four new halogenated chamigrenes have been isolated from the sea hare, the (E)-and (Z)-9-(bromomethylidene)-1,2,5-trimethylspiro[5.5]undeca-l,7-dien-3-ones (11 and 10, resp.) the structures of which were deduced by NMR spectroscopy and by comparison with a known relative, the (8R,9R)-8-bromo-9-chlor

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Marine natural products: Dactyloxene-B, a sesquiterpene ether from the sea hare, Aplysia dactylomela

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ChemInform Abstract: Aplysiols A and B,

ChemInform Abstract: Aplysiols A and B, Squalene-Derived Polyethers from the Mantle of the Sea Hare Aplysia dactylomela.

✍ Emiliano Manzo; Margherita Gavagnin; Giuseppe Bifulco; Paola Cimino; Simone Di M 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 23 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Aplydactone, a New

ChemInform Abstract: Aplydactone, a New Sesquiterpenoid with an Unprecedented Carbon Skeleton from the Sea Hare Aplysia dactylomela, and Its Cargill-Like Rearrangement.

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Structure and absolute configuration of

Structure and absolute configuration of a new rearranged chamigrane-type sesquiterpenoid from the sea hare Aplysia sp.

✍ Sergei N Fedorov; Larisa K Shubina; Anatoly I Kalinovsky; Ekaterina G Lyakhova; 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 145 KB

6S,10S)-3,10- Dimethyl-7,11-dimethylidenespiro[5,5]undec-2-en-4-one (1), a new rearranged chamigrane-type sesquiterpenoid with two sp 2 -hybridized carbons in α-positions to the spiro-atom, was isolated from the alcoholic extract of the sea hare Aplysia sp. and its structure and absolute configurati