@article {2684,
	title = {Development of an Oxazole Conjunctive Reagent and Application to the Total Synthesis of Siphonazoles},
	journal = {Journal of Organic Chemistry},
	volume = {74},
	number = {23},
	year = {2009},
	note = {ISI Document Delivery No.: 523ONTimes Cited: 6Cited Reference Count: 120Zhang, Jianmin Polishchuk, Elena A. Chen, Jie Ciufolini, Marco A.},
	month = {Dec},
	pages = {9140-9151},
	type = {Review},
	abstract = {The preparation of 4-carbethoxy-5-methyl-2-(phenylsulfonyl)methyloxizole and Its use in the elaboration of more complex oxazoles are described. A total synthesis of the unique natural products siphonazoles A and B, illustrates an application of this building block. A discussion of the biological activity of the siphonazoles is also presented.},
	keywords = {1ST TOTAL-SYNTHESIS, ALLENYL ESTERS, CONJUGATED, CYANOBACTERIUM NOSTOC-MUSCORUM, CYTOTOXIC, DIAZONAMIDE-A, DOUBLE ELIMINATION PROTOCOL, GLYOXYLIC-ACID DERIVATIVES, INTRAMOLECULAR HYDROAMINATION, marine sponge, METABOLITES, NATURAL-PRODUCT HENNOXAZOLE},
	isbn = {0022-3263},
	url = {<Go to ISI>://000272083700026},
	author = {Zhang, J. M. and Polishchuk, E. A. and Chen, J. and Ciufolini,Marco A.}
}
@article {2127,
	title = {Autophagy-modulating aminosteroids isolated from the sponge Cliona celata},
	journal = {Organic Letters},
	volume = {10},
	number = {14},
	year = {2008},
	note = {ISI Document Delivery No.: 326ABTimes Cited: 4Cited Reference Count: 18Keyzers, Robert A. Daoust, Julie Davies-Coleman, Michael T. Van Soest, Rob Balgi, Aruna Donohue, Elizabeth Roberge, Michel Andersen, Raymond J.},
	month = {Jul},
	pages = {2959-2962},
	type = {Article},
	abstract = {Clionamines A-D (1-4), new aminosteroids that modulate autophagy, have been isolated from South African specimens of the sponge Cliona celata. Clionamine D (4) has an unprecedented spiro bislactone side chain.},
	keywords = {2 STEROIDAL ALKALOIDS, CORTICIUM SP, marine sponge, YEAST},
	isbn = {1523-7060},
	url = {<Go to ISI>://000257629200011},
	author = {Keyzers, R. A. and Daoust, J. and Davies-Coleman, M. T. and Van Soest, R. and Balgi, A. and Donohue, E. and Roberge, M. and Andersen, R. J.}
}
@article {1029,
	title = {Pachymoside A - A novel glycolipid isolated from the marine sponge Pachymatisma johnstonia},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {82},
	number = {2},
	year = {2004},
	note = {ISI Document Delivery No.: 802BHTimes Cited: 5Cited Reference Count: 21},
	month = {Feb},
	pages = {102-112},
	type = {Article},
	abstract = {Crude extracts of the North Sea marine sponge Pachymatisma johnstonia showed promising activity in a new assay for inhibitors of bacterial type III secretion. Bioassay-guided fractionation resulted in the isolation of the pachymosides, a new family of sponge glycolipids. A major part of the structural diversity in this family of glycolipids involves increasing degrees of acetylation and differing positions of acetylation on a common pachymoside glycolipid template. All of the metabolites with these variations in acetylation pattern were converted into the same peracetylpachymoside methyl ester (2) for purification and spectroscopic analysis. Pachymoside A (1) is the component of the mixture that has natural acetylation at the eight galactose hydroxyls and at the C-6 hydroxyls of glucose-B and glucose-D. Chemical degradation and transformation in conjunction with extensive analysis of 800 MHz NMR data was used to elucidate the structure of pachymoside A (1).},
	keywords = {BACTERIAL VIRULENCE, ENTEROPATHOGENIC ESCHERICHIA-COLI, glycolipid, GLYCOSPHINGOLIPIDS, HOST-CELLS, III SECRETION, inhibitors, marine sponge, NATURAL-PRODUCTS, Pachymatisma johnstonia, pachymoside, PLAKORTIS-SIMPLEX, PLAKOSIDE, PRENYLATED, RECEPTOR},
	isbn = {0008-4042},
	url = {<Go to ISI>://000220138500006},
	author = {Warabi, K. and Zimmerman, W. T. and Shen, J. K. and Gauthier, A. and Robertson, M. and Finlay, B. B. and Van Soest, R. and Andersen, R. J.}
}
@article {783,
	title = {Isoarenarol, a new protein kinase inhibitor from the marine sponge Dysidea arenaria},
	journal = {Pharmaceutical Biology},
	volume = {41},
	number = {4},
	year = {2003},
	note = {ISI Document Delivery No.: 714EDTimes Cited: 10Cited Reference Count: 7},
	month = {Jun},
	pages = {223-225},
	type = {Article},
	abstract = {The novel sesquiterpene hydroquinone isoarenarol (1) and the known compound arenarol (2) were isolated from extracts of the marine sponge Dysidea arenaria Bergquist as part of a search for new protein kinase inhibitors. Both 1 and 2 showed potent and selective protein kinase inhibition in vitro.},
	keywords = {AVAROL, hydroquinone, kinase inhibitor, marine sponge, Papua New Guinea, sesquiterpene},
	isbn = {1388-0209},
	url = {<Go to ISI>://000184898600001},
	author = {Yoo, H. D. and Leung, D. and Sanghara, J. and Daley, D. and Van Soest, R. and Andersen, R. J.}
}
@article {4513,
	title = {New geodiamolides from the sponge Cymbastela sp collected in Papua New Guinea},
	journal = {Journal of Natural Products},
	volume = {62},
	number = {8},
	year = {1999},
	note = {ISI Document Delivery No.: 232QMTimes Cited: 19Cited Reference Count: 15},
	month = {Aug},
	pages = {1137-1141},
	type = {Article},
	abstract = {Geodiamolides J-P (11-17) and R (19), eight new cyclic depsipetides, have been isolated from the marine sponge Cymbastela sp. collected in Papua New Guinea. The serine residue in geodiamolides L-P (13-17) and R (19) has not been previously found in this family of compounds.},
	keywords = {ANTIFUNGAL ACTIVITY, CHONDROMYCES-CROCATUS MYXOBACTERIA, CYCLODEPSIPEPTIDES, CYTOTOXIC PEPTIDES, GEODIA SP, marine sponge},
	isbn = {0163-3864},
	url = {<Go to ISI>://000082381500014},
	author = {Coleman, J. E. and Van Soest, R. and Andersen, R. J.}
}
