@article {749,
	title = {Briarane, erythrane, and aquariane diterpenoids from the Caribbean gorgonian Erythropodium caribaeorum},
	journal = {European Journal of Organic Chemistry},
	number = {18},
	year = {2003},
	note = {ISI Document Delivery No.: 726HFTimes Cited: 5Cited Reference Count: 15},
	month = {Sep},
	pages = {3515-3523},
	type = {Article},
	abstract = {Seven new diterpenoids belonging to the briarane [erythrolides R (5), S (6), T (7), and U (8)], erythrane [erythrolide V (9)], and aquariane [aquariolides B (10) and C (11)] skeletal classes have been isolated from the encrusting gorgonian Erythropodium caribaeorum. The structures of the new compounds were elucidated by spectroscopic analysis and chemical interconversions. A biogenetic proposal that links carbon skeletons found in E. caribaeorum diterpenoids is presented. (C) Wiley-VCH Verlag GmbH Co.},
	keywords = {asymmetric, bioorganic chemistry, ELEUTHEROBIN, ERYTHROLIDES, natural products, structure elucidation, SYNTHESIS, terpenoids},
	isbn = {1434-193X},
	url = {<Go to ISI>://000185592300005},
	author = {Taglialatela-Scafati, O. and Craig, K. S. and Reberioux, D. and Roberge, M. and Andersen, R. J.}
}
@article {5071,
	title = {Evidence for the biosynthesis of squalene via the methylerythritol phosphate pathway in a Streptomyces sp obtained from a marine sediment},
	journal = {Journal of Organic Chemistry},
	volume = {66},
	number = {18},
	year = {2001},
	note = {ISI Document Delivery No.: 470LVTimes Cited: 6Cited Reference Count: 23},
	month = {Sep},
	pages = {6202-6206},
	type = {Article},
	keywords = {2-C-METHYL-D-ERYTHRITOL, 4-(CYTIDINE, 4-PHOSPHATE, 5{\textquoteright}-DIPHOSPHO)-2-C-METHYL-D-ERYTHRITOL, BACTERIA, HIGHER-PLANTS, ISOPRENOID BIOSYNTHESIS, MEVALONATE-INDEPENDENT PATHWAY, NONMEVALONATE PATHWAY, PRECURSOR, terpenoids},
	isbn = {0022-3263},
	url = {<Go to ISI>://000170874200039},
	author = {Fontana, A. and Kelly, M. T. and Prasad, J. D. and Andersen, R. J.}
}
@article {3946,
	title = {New terpenoid metabolites from the skin extracts, an egg mass, and dietary sponges of the Northeastern Pacific dorid nudibranch Cadlina luteomarginata},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {6},
	year = {1997},
	note = {ISI Document Delivery No.: XL704Times Cited: 27Cited Reference Count: 26},
	month = {Jun},
	pages = {773-789},
	type = {Article},
	abstract = {Chemical investigations of Cadlina luteomarginata skin extracts, egg masses, and dietary sponges have led to the identification of the novel terpenoids cadlinaldehyde (30), spongian 32, seco-spongian 35, 20-acetoxy-12-marginatone (38), and lutenolide (39) from the nudibranch skin extracts, the new drimane sesquiterpenoid 1 alpha,2 alpha-diacetoxyalbicanyl acetate (40) from the nudibranch{\textquoteright}s egg mass, and the new sesquiterpenoids O-methyl-9-oxofurodysininlactone (47), 2-oxomicrocionin-2-lactone (48), and O-methyl-2-oxomicrocionin-2-lactone (49), from the dietary sponge Pleraplysilla sp. The known terpenoids furodysinin (1), furodysin (16), marginatafuran (21), and 9,11-dihydrogracillin A (37), which have been frequently isolated from C. luteomarginata skin extracts, were found for the first time in extracts of the dietary sponges Pleraplysilla sp. and Aplysilla sp. One of the new terpenoids, cadlinaldehyde (30), has an unprecedented degraded sesterterpenoid skeleton.},
	keywords = {APLYSILLA-GLACIALIS, CHEMICAL DEFENSE, MOLLUSKS, nudibranch, SPONGE, structure elucidation, terpenoids},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997XL70400025},
	author = {Dumdei, E. J. and Kubanek, J. and Coleman, J. E. and Pika, J. and Andersen, R. J. and Steiner, J. R. and Clardy, J.}
}
