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Acyclic stereocontrol in catalyzed intramolecular Diels-Alder cyclizations leading to octahydronaphthalenecarboxaldehydesMARSHALL, J. A; GROTE, J; AUDIA, J. E et al.Journal of the American Chemical Society. 1987, Vol 109, Num 4, pp 1186-1194, issn 0002-7863Article

An application of the Ireland reaction to the stereospecific synthesis of fused carbocyclic systemsDANISHEFSKY, S. J; AUDIA, J. E.Tetrahedron letters. 1988, Vol 29, Num 12, pp 1371-1374, issn 0040-4039Article

Total synthesis of the Fusarium toxin equisetin: proof of the stereochemical relationship of the tetramate and terpenoid sectorsTUROS, E; AUDIA, J. E; DANISHEFSKY, S. J et al.Journal of the American Chemical Society. 1989, Vol 111, Num 21, pp 8231-8236, issn 0002-7863, 6 p.Article

Acyclic stereocontrol in catalyzed intramolecular Diels―Alder cyclizations of 4-methyl-2,8,10-undecatrienalsMARSHALL, J. A; AUDIA, J. E; GROTE, J et al.Journal of organic chemistry. 1986, Vol 51, Num 7, pp 1155-1157, issn 0022-3263Article

Intramolecular Diels-Alder cyclization of conjugated aldehydes: synthesis of a chlorothricolide intermediateMARSHALL, J. A; AUDIA, J. E; GROTE, J et al.Journal of organic chemistry. 1984, Vol 49, Num 26, pp 5277-5279, issn 0022-3263Article

Species differences in the pharmacology of the 5-hydroxytryptamine₂ receptor : strucutally specific differentiation by ergolines and tryptaminesNELSON, D. L; LUCAITES, V. L; AUDIA, J. E et al.The Journal of pharmacology and experimental therapeutics. 1993, Vol 265, Num 3, pp 1272-1279, issn 0022-3565Article

Conjugate addition of organocuprates to trans-4a,5,6,7,8,8a-hexahydronaphthalene-1-carboxaldehydes: synthesis of a chlorothricin degradation productMARSHALL, J. A; AUDIA, J. E; SHEARER, B. G et al.Journal of organic chemistry. 1986, Vol 51, Num 10, pp 1730-1735, issn 0022-3263Article

Synthesis of the individual enantiomers of the benzoquinolinone human type 1 steroid 5-α-reductase inhibitors LY191704 and LY266111AUDIA, J. E; LAWHORN, D. E; DEETER, J. B et al.Tetrahedron letters. 1993, Vol 34, Num 44, issn 0040-4039, 6959, 7001-7004 [5 p.]Article

Amyloid β-mediated oxidative and metabolic stress in rat cortical neurons : No direct evidence for a role for H₂O₂ generationZHANG, Z; RYDEL, R. E; DRZEWIECKI, G. J et al.Journal of neurochemistry. 1996, Vol 67, Num 4, pp 1595-1606, issn 0022-3042Article

Comparison of desmethylsertraline with sertraline as a monoamine uptake inhibitor in vivoFULLER, R. W; HEMRICK-LUECKE, S. K; LITTLEFIELD, E. S et al.Progress in neuro-psychopharmacology & biological psychiatry. 1995, Vol 19, Num 1, pp 135-149, issn 0278-5846Article

Nonsteroidal inhibitors of human type I steroid 5-α-reductaseJONES, C. D; AUDIA, J. E; LAWHORN, D. E et al.Journal of medicinal chemistry (Print). 1993, Vol 36, Num 3, pp 421-423, issn 0022-2623Article

Functional gamma-secretase inhibitors reduce beta-amyloid peptide levels in brainDOVEY, H. F; JOHN, V; HU, K. L et al.Journal of neurochemistry. 2001, Vol 76, Num 1, pp 173-181, issn 0022-3042Article

5-HT_1F receptor agonists inhibit neurogenic dural inflammation in guinea pigsJOHNSON, K. W; SCHAUS, J. M; PHEBUS, L. A et al.Neuroreport (Oxford). 1997, Vol 8, Num 9-10, pp 2237-2240, issn 0959-4965Article

LY191704 inhibits type I steroid 5α-reductase in human scalpNEUBAUER, B. L; GRAY, H. M; TINDALL, D. J et al.The Journal of clinical endocrinology and metabolism. 1996, Vol 81, Num 6, pp 2055-2060, issn 0021-972XArticle

Potent, selective tetrahydro-β-carboline antagonists of the serotonin 2B (5HT_2B) contractile receptor in the rat stomach fundusAUDIA, J. E; EVRARD, D. A; MURDOCH, G. R et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 14, pp 2773-2780, issn 0022-2623Article

Kinetic analysis of LY320236 : competitive inhibitor of type I and non-competitive inhibitor of type II human steroid 5α-reductaseMCNULTY, A. M; AUDIA, J. E; BEMIS, K. G et al.Journal of steroid biochemistry and molecular biology. 2000, Vol 72, Num 1-2, pp 13-21, issn 0960-0760Article

Synthesis and 5α-reductase inhibitory activity of 8-substituted benzo[f]quinolinones derived from palladium mediated coupling reactionsSMITH, E. C. R; MCQUAID, L. A; GOODE, R. L et al.Bioorganic & medicinal chemistry letters (Print). 1998, Vol 8, Num 4, pp 395-398, issn 0960-894XArticle

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Diels-Alder cyclization of 2,8,10-undecatrienals as a route to 1,2,3,4,4a,5,6,8a-octahydronaphthalenesMARSHALL, J. A; AUDIA, J. E; GROTE, J et al.Tetrahedron (Oxford. Print). 1986, Vol 42, Num 11, pp 2893-2902, issn 0040-4020Article

Responses of LNCaP prostatic adenocarcinoma cell cultures to LY300502, a benzoquinolinone human type I 5α-reductase inhibitorSUTKOWSKI, D. M; AUDIA, J. E; GOODE, R. L et al.The Prostate. 1996, pp 62-66, issn 0270-4137, SUP6Conference Paper

N(1-)-substituted ergolines and tryptamines show species differences for the agonist-labeled 5-HT₂ receptorJOHNSON, M. P; AUDIA, J. E; NISSEN, J. S et al.European journal of pharmacology. 1993, Vol 239, Num 1-3, pp 111-118, issn 0014-2999Article

Synthesis of two useful, enenatiomerically pure derivatives of (S)-4-hydroxy-2-cyclohexenoneAUDIA, J. E; BOISVERT, L; PATTEN, A. D et al.Journal of organic chemistry. 1989, Vol 54, Num 15, pp 3738-3740, issn 0022-3263, 3 p.Article

N-methyl-5-tert-butyltryptamine : A novel, highly potent 5-HT_1D receptor agonistXU, Y.-C; SCHAUS, J. M; WALKER, C et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 3, pp 526-531, issn 0022-2623Article

Characterization of type I 5α-reductase activity in DU145 human prostatic adenocarcinoma cellsKAEFER, M; AUDIA, J. E; NEUBAUER, B. L et al.Journal of steroid biochemistry and molecular biology. 1996, Vol 58, Num 2, pp 195-205, issn 0960-0760Article