A new synthesis of 3-arylthioindoles as selective COX-2 inhibitors using PIFA von Campbell, Jeffrey A, Broka, Chris A, Gong, Leyi, Walker, Keith A.M, Wang, Jin-Hai

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Preparation of 3-arylmethylindoles as selective COX-2 inhibitors von Campbell, Jeffrey A, Bordunov, Viola, Broka, Chris A, Dankwardt, John, Hendricks, Robert T, Kress, James M, Walker, Keith A.M, Wang, Jin-Hai

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Rational design of 6-methylsulfonylindoles as selective cyclooxygenase-2 inhibitors von Campbell, Jeffrey A., Bordunov, Viola, Broka, Chris A., Browner, Michelle F., Kress, James M., Mirzadegan, Tara, Ramesha, Chakk, Sanpablo, Bong F., Stabler, Russell, Takahara, Patricia, Villasenor, Armando, Walker, Keith A.M., Wang, Jin-Hai, Welch, Mary, Weller, Paul

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4′-Substituted nucleosides as inhibitors of HIV: an unusual oxetane derivative von O-Yang, Counde, Kurz, Walter, Eugui, Elsie M., McRoberts, Mary Jane, Verheyden, Julien P.H., Kurz, Lilia J., Walker, Keith A.M

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Design and synthesis of orally active inhibitors of TNF synthesis as anti-rheumatoid arthritis drugs von Chen, Jian Jeffrey, Dewdney, Nolan, Lin, Xiaohong, Martin, Robert L, Walker, Keith A.M, Huang, Jane, Chu, Frances, Eugui, Elsie, Mirkovich, Anna, Kim, Yong, Sarma, Keshab, Arzeno, Humberto, Van Wart, Harold E

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Synthesis of 4′-cyanothymidine and analogs as potent inhibitors of HIV von O-Yang, Counde, Wu, Helen Y., Fraser-Smith, Elizabeth B., Walker, Keith A.M.

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Solid-phase synthesis of di- and tripeptidic hydroxamic acids as inhibitors of procollagen C-proteinase von Dankwardt, Sharon M, Billedeau, Roland J, Lawley, Linda K, Abbot, Sarah C, Martin, Robert L, Chan, Christine S, Van Wart, Harold E, Walker, Keith A.M

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Novel Series of Dihydropyridinone P2X7 Receptor Antagonists von Lopez-Tapia, Francisco, Walker, Keith A. M, Brotherton-Pleiss, Christine, Caroon, Joanie, Nitzan, Dov, Lowrie, Lee, Gleason, Shelley, Zhao, Shu-Hai, Berger, Jacob, Cockayne, Debra, Phippard, Deborah, Suttmann, Rebecca, Fitch, William L, Bourdet, David, Rege, Pankaj, Huang, Xiaojun, Broadbent, Scott, Dvorak, Charles, Zhu, Jiang, Wagner, Paul, Padilla, Fernando, Loe, Brad, Jahangir, Alam, Alker, André

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Synthesis of analogs of prostacyclin containing a thiazone ring von H. Bradbury, Robert, Walker, Keith A.M

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Lactams as EP4 Prostanoid Receptor Agonists. 3. Discovery of N-Ethylbenzoic Acid 2-Pyrrolidinones as Subtype Selective Agents von Elworthy, Todd R, Brill, Emma R, Chiou, San-San, Chu, Frances, Harris, Jason R, Hendricks, R. Than, Huang, Jane, Kim, Woongki, Lach, Leang K, Mirzadegan, Tara, Yee, Calvin, Walker, Keith A. M

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Crystal structures of MMP-1 and -13 reveal the structural basis for selectivity of collagenase inhibitors von Lovejoy, Brett, Welch, Anthony R., Carr, Steven, Luong, Christine, Broka, Chris, Hendricks, R. Than, Campbell, Jeffery A., Walker, Keith A.M., Martin, Robert, Van Wart, Harold, Browner, Michelle F.

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A convenient preparation of thioethers from alcohols von Walker, Keith A.M

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Stereoisomers of ketoconazole: preparation and biological activity von Rotstein, David M, Kertesz, Denis J, Walker, Keith A. M, Swinney, David C

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Amino acid derived sulfonamide hydroxamates as inhibitors of procollagen C-proteinase. Part 2: Solid-phase optimization of side chains von DANKWARDT, Sharon M, ABBOT, Sarah C, BROKA, Chris A, MARTIN, Robert L, CHAN, Christine S, SPRINGMAN, Eric B, VAN WART, Harold E, WALKER, Keith A. M

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Amino acid derived sulfonamide hydroxamates as inhibitors of procollagen C-Proteinase: solid-Phase synthesis of ornithine analogues von Dankwardt, Sharon M., Martin, Robert L., Chan, Christine S., Van Wart, Harold E., Walker, Keith A.M., Delaet, Nancy G., Robinson, Leslie A.

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Corrigendum to “Preparation of 3-arylmethylindoles as selective COX-2 inhibitors”: [Tetrahedron Lett. 45 (2004) 3793] von Campbell, Jeffrey A, Bordunov, Viola, Broka, Chris A, Dankwardt, John, Hendricks, Robert T, Kress, James M, Walker, Keith A.M, Wang, Jin-Hai

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A revised mechanism for the Mitsunobu reaction von Varasi, Mario, Walker, Keith A. M, Maddox, Michael L

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Corrigendum to “Amino acid derived sulfonamide hydroxamates as inhibitors of procollagen C-proteinase: solid-phase synthesis of ornithine analogues”[Bioorg. Med. Chem. Lett. 11 (20... von Dankwardt, Sharon M, Martin, Robert L, Chan, Christine S, Van Wart, Harold E, Walker, Keith A.M, Delaet, Nancy G, Robinson, Leslie A

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3,4-Dihydroquinolin-2(1H)-ones as combined inhibitors of thromboxane A2 synthase and cAMP phosphodiesterase von Martinez, Gregory R, Walker, Keith A. M, Hirschfeld, Donald R, Bruno, John J, Yang, Diana S, Maloney, Patrick J

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Azalanstat (RS-21607), a lanosterol 14α-demethylase inhibitor with cholesterol-lowering activity von Burton, Pamela M., Swinney, David C., Heller, Renu, Dunlap, Bonnie, Chiou, Melody, Malonzo, Edna, Haller, Judy, Walker, Keith A.M., Salari, Amid, Murakami, Stanley, Mendizabal, Gregory, Tokes, Laszlo

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