Oxygen Consumption is Limited at an Ecologically Relevant Rearing Temperature in Pupfish Eggs von Jones, Alexander C., Lim, David, Wayne-Thompson, Jacoby J., Urbina, Natasha, Puentedura, Georgina, Hillyard, Stanley, Breukelen, Frank Van

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A priori prediction of activity for HIV-1 protease inhibitors employing energy minimization in the active site von Holloway, M. Katharine, Wai, Jenny M, Halgren, Thomas A, Fitzgerald, Paula M. D, Vacca, Joseph P, Dorsey, Bruce D, Levin, Rhonda B, Thompson, Wayne J, Chen, L. Jenny

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3-Tetrahydrofuran and pyran urethanes as high-affinity P2-ligands for HIV-1 protease inhibitors von Ghosh, Arun K, Thompson, Wayne J, McKee, Sean P, Duong, Tien T, Lyle, Terry A, Chen, Jenny C, Darke, Paul L, Zugay, Joan A, Emini, Emilio A

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Potent HIV protease inhibitors: the development of tetrahydrofuranylglycines as novel P2-ligands and pyrazine amides as P3-ligands von Ghosh, Arun K, Thompson, Wayne J, Holloway, M. Katharine, McKee, Sean P, Duong, Tien T, Lee, Hee Yoon, Munson, Peter M, Smith, Anthony M, Wai, Jenny M, Darke, Paul L, Zugay, Joan A, Emini, Emilio A, Schleif, William A, Huff, Joel R, Anderson, Paul S

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The Development of Cyclic Sulfolanes as Novel and High-Affinity P2 Ligands for HIV-1 Protease Inhibitors von Ghosh, Arun K, Lee, Hee Yoon, Thompson, Wayne J, Culberson, Chris, Holloway, M. Katharine, McKee, Sean P, Munson, Peter M, Duong, Tien T, Smith, Anthony M

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An efficient synthesis of arylpyrazines and bipyridines von Thompson, Wayne J, Jones, James H, Lyle, Paulette A, Thies, J. Eric

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Synthesis and pharmacological evaluation of a series of dibenzo[a,d]cycloalkenimines as N-methyl-D-aspartate antagonists von Thompson, Wayne J, Anderson, Paul S, Britcher, Susan F, Lyle, Terry A, Thies, J. Eric, Magill, Catherine A, Varga, Sandor L, Schwering, John E, Lyle, Paulette A

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Nonpeptidal P2 Ligands for HIV Protease Inhibitors:  Structure-Based Design, Synthesis, and Biological Evaluation von Ghosh, Arun K, Kincaid, John F, Walters, D. Eric, Chen, Yan, Chaudhuri, Narayan C, Thompson, Wayne J, Culberson, Chris, Fitzgerald, Paula M. D, Lee, Hee Yoon, McKee, Sean P, Munson, Peter M, Duong, Tien T, Darke, Paul L, Zugay, Joan A, Schleif, William A, Axel, Melinda G, Lin, Juinn, Huff, Joel R

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A general synthesis of 5-arylnicotinates von Thompson, Wayne J, Gaudino, John

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N,N'-disuccinimidyl carbonate : a useful reagent for alkoxycarbonylation of amines von GHOSH, A. K, DUONG, T. T, MCKEE, S. P, THOMPSON, W. J

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An approach to the total synthesis of chlorothricolide: the synthesis of the top half von Ireland, Robert E, Thompson, Wayne J

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Structure-Based Design of HIV-1 Protease Inhibitors: Replacement of Two Amides and a 10.pi.-Aromatic System by a Fused Bis-tetrahydrofuran von Ghosh, Arun K, Thompson, Wayne J, Fitzgerald, Paula M. D, Culberson, J. Chris, Axel, Melinda G, McKee, Sean P, Huff, Joel R, Anderson, Paul S

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Stereoselective synthesis of desmethoxy-(+)-verruculogen TR-2 von Boyd, Steven A, Thompson, Wayne J

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An efficient synthesis of hydroxyethylene dipeptide isosteres: the core unit of potent HIV-1 protease inhibitors von Ghosh, Arun K, McKee, Sean P, Thompson, Wayne J

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Benzocycloalkyl amines as novel C-termini for HIV protease inhibitors von Lyle, Terry A, Wiscount, Catherine M, Guare, James P, Thompson, Wayne J, Anderson, Paul S, Darke, Paul L, Zugay, Joan A, Emini, Emilio A, Schleif, William A

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Cyclic sulfone-3-carboxamides as novel P2-ligands for Ro 31-8959 based HIV-1 protease inhibitors von Ghosh, Arun K., Thompson, Wayne J., Munson, Peter M., Liu, Wenming, Huff, Joel R.

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Potent HIV-1 protease inhibitors: stereoselective synthesis of a dipeptide mimic von Ghosh, Arun K, McKee, Sean P, Thompson, Wayne J, Darke, Paul L, Zugay, Joan C

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Cyclic sulfone-3-carboxamides as novel P 2-ligands for Ro 31-8959 based HIV-1 protease inhibitors von Ghosh, Arun K., Thompson, Wayne J., Munson, Peter M., Liu, Wenming, Huff, Joel R.

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A highly enantioselective synthesis of phosphate triesters von Nakayama, Kensaku, Thompson, Wayne J

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3'-Tetrahydrofuranylglycine as a novel, unnatural amino acid surrogate for asparagine in the design of inhibitors of the HIV protease von Thompson, Wayne J, Ghosh, Arun K, Holloway, M. Katharine, Lee, Hee Yoon, Munson, Peter M, Schwering, John E, Wai, Jenny, Darke, Paul L, Zugay, Joan

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