@article {126,
	title = {Aflaquinolones A-G: Secondary metabolites from marine and fungicolous isolates of Aspergillus spp.},
	journal = {Journal of Natural Products},
	volume = {75},
	year = {2012},
	note = {CAPLUS AN 2012:163288(Journal; Online Computer File)},
	pages = {464 - 472},
	publisher = {American Chemical Society-American Society of Pharmacognosy},
	abstract = {Seven new compds. (aflaquinolones A-G; 1-7) contg. dihydroquinolin-2-one and terpenoid units have been isolated from two different fungal sources.  Two of these metabolites (1 and 2) were obtained from a Hawaiian fungicolous isolate of Aspergillus sp. (section Flavipedes; MYC-2048 = NRRL 58570), while the others were obtained from a marine Aspergillus isolate (SF-5044) collected in Korea.  The structures of these compds. were detd. mainly by anal. of NMR and MS data.  Relative and abs. configurations were assigned on the basis of NOESY data and 1H NMR J-values, comparison of calcd. and exptl. ECD spectra, and anal. of a Mosher{\textquoteright}s ester deriv. of 2.  Several known compds., including alantrypinone, aspochalasins I and J, Me 3,4,5-trimethoxy-2((2-((3-pyridinylcarbonyl)amino)benzoyl)amino)benzoate, and trans-dehydrocurvularin were also encountered in the ext. of the Hawaiian isolate. [on SciFinder(R)]},
	keywords = {aflaquinolone Aspergillus},
	isbn = {0163-3864},
	author = {Neff, Scott A. and Lee, Sang Un and Asami, Yukihiro and Ahn, Jong Seog and Oh, Hyuncheol and Baltrusaitis, Jonas and Gloer, James B. and Wicklow, Donald T.}
}
@article {155,
	title = {Phomalevones A-C: Dimeric and pseudodimeric polyketides from a fungicolous Hawaiian isolate of Phoma sp. (Cucurbitariaceae).},
	journal = {Journal of Natural Products},
	volume = {74},
	year = {2011},
	note = {CAPLUS AN 2011:84225(Journal; Online Computer File)},
	month = {2011///},
	pages = {395 - 401},
	publisher = {American Chemical Society-American Society of Pharmacognosy},
	abstract = {Phomalevones A-C (1-3), three new compds. with bis-dihydroxanthone and bis-benzophenone systems, were isolated from cultures of a Hawaiian isolate of Phoma sp. (MYC-1734 = NRRL 39060; Cucurbitariaceae).  The structures of 1-3 were detd. by anal. of NMR and MS data.  The abs. configurations of the sp3 stereocenters in the monomeric unit of 1 were assigned by application of Mosher{\textquoteright}s method, and overall abs. configurations were proposed on the basis of ECD data using both computational methods and comparisons with literature data for model compds.  All three compds. showed antibacterial activity, and compds. 2 and 3 also exhibited antifungal effects. [on SciFinder(R)]},
	keywords = {phomalevone Phoma},
	isbn = {0163-3864},
	author = {Shim, Sang Hee and Baltrusaitis, Jonas and Gloer, James B. and Wicklow, Donald T.}
}
@article {167,
	title = {Hymenopsins A and B and a macrophorin analog from a fungicolous Hymenopsis sp.},
	journal = {Journal of Natural Products},
	volume = {73},
	year = {2010},
	note = {CAPLUS AN 2009:1462186(Journal)},
	month = {2010///},
	pages = {404 - 408},
	publisher = {American Chemical Society-American Society of Pharmacognosy},
	abstract = {Hymenopsin A (1), hymenopsin B (2), and a new macrophorin analog, 2{\textquoteright},3{\textquoteright}-epoxy-13-hydroxy-4{\textquoteright}-oxomacrophorin A (3), have been isolated from a fungicolous isolate of Hymenopsis sp. (MYC-1703; NRRL 37638).  The structures and relative configurations of these compds. were assigned on the basis of 2D NMR and MS data, and the identity of 1 was confirmed by X-ray crystallog. anal.  The abs. configuration of 2 was proposed on the basis of CD anal. using both empirical and computational methods.  Compds. 2 and 3 showed antibacterial activity against Staphylococcus aureus and Bacillus subtilis.  Compd. 3 was also active against Aspergillus flavus and Fusarium verticillioides. [on SciFinder(R)]},
	keywords = {hymenopsin Hymenopsis},
	isbn = {0163-3864},
	author = {Schmidt, Lori E. and Deyrup, Stephen T. and Baltrusaitis, Jonas and Swenson, Dale C. and Wicklow, Donald T. and Gloer, James B.}
}
