Journal of Natural Products · 2010 · 51 citations · 10 references
Seventeen diterpenes featuring the dolabellane skeleton (1-17) were isolated from the organic extracts of the brown alga Dilophus spiralis. Seven compounds are new natural products (1, 3, 5, 6, 11, 14, 15) and eight are structurally revised (2, 4, 7-10, 12, 13), among which three are reported for the first time from a natural source (4, 9, 10). The structure elucidation and the assignment of the relative configurations of the isolated natural products were based on detailed analyses of their spectroscopic data. The structure of metabolite 10 was confirmed by single-crystal X-ray diffraction analysis, whereas the absolute configurations of compounds 2, 4-10, 12, and 13 were determined using the modified Mosher's method on the semisynthetic product 18 and chemical interconversions. The antibacterial activities of compounds 1-18 were evaluated against six strains of Staphylococcus aureus, including multidrug- and methicillin-resistant variants.
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John W. Blunt, Brent R. Copp, Murray H. G. Munro et al. · Natural Product Reports · 2010 · 407 citations · Full text
Diterpenes from Dolabella californica
Chris Ireland, D. John Faulkner · The Journal of Organic Chemistry · 1977 · 68 citations
Diterpenes based on the dolabellane skeleton from dictyota dichotoma
Vincenzo Amico, Giovanna Oriente, Mario Piattelli et al. · Tetrahedron · 1980 · 57 citations
Biology, Protist, Phylogenetics +4
New diterpenoids from the alga Dictyota dichotoma
Rosario Durán, Marı́a J. Ortega, Javier Salvá · Tetrahedron · 1997 · 54 citations