Transition-metal promoted hydroborations of alkenes, emerging methodology for organic transformations von Burgess, Kevin, Ohlmeyer, Michael J

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Identification and optimization of novel 2-(4-oxo-2-aryl-quinazolin-3(4 H)-yl)acetamide vasopressin V3 (V1b) receptor antagonists von Letourneau, Jeffrey J., Riviello, Christopher M., Li, Hong, Cole, Andrew G., Ho, Koc-Kan, Zanetakos, Heather A., Desai, Hema, Zhao, Jiuqiao, Auld, Douglas S., Napier, Susan E., Thomson, Fiona J., Goan, Katharine A., Morphy, J. Richard, Ohlmeyer, Michael H.J., Webb, Maria L.

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Identification and hit-to-lead optimization of a novel class of CB1 antagonists von Letourneau, Jeffrey J., Jokiel, Patrick, Olson, John, Riviello, Christopher M., Ho, Koc-Kan, McAleer, Lihong, Yang, Jingchun, Swanson, Robert N., Baker, James, Cowley, Phillip, Edwards, Darren, Ward, Nick, Ohlmeyer, Michael H.J., Webb, Maria L.

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2-Benzimidazolyl-9-(chroman-4-yl)-purinone derivatives as JAK3 inhibitors von Cole, Andrew G., Bohnstedt, Adolph C., Paradkar, Vidyadhar, Kingsbury, Celia, Quintero, Jorge G., Park, Haengsoon, Lu, Yingchun, You, Ming, Neagu, Irina, Diller, David J., Letourneau, Jeffrey J., Shao, Yuefei, James, Ray A., Riviello, Christopher M., Ho, Koc-Kan, Lin, Tsung H., Wang, Bojing, Appell, Kenneth C., Sills, Matthew, Quadros, Elizabeth, Kimble, Earl F., Ohlmeyer, Michael H.J., Webb, Maria L.

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Novel Pyrrolidine Ureas as C−C Chemokine Receptor 1 (CCR1) Antagonists von Merritt, J. Robert, Liu, Jinqi, Quadros, Elizabeth, Morris, Michelle L, Liu, Ruiyan, Zhang, Rui, Jacob, Biji, Postelnek, Jennifer, Hicks, Catherine M, Chen, Weiqing, Kimble, Earl F, Rogers, W. Lynn, O’Brien, Linda, White, Nicole, Desai, Hema, Bansal, Shalini, King, George, Ohlmeyer, Michael J, Appell, Kenneth C, Webb, Maria L

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Enantioselective hydroboration mediated by homochiral rhodium catalysts von Burgess, Kevin, Ohlmeyer, Michael J

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Novel pyrrolidine heterocycles as CCR1 antagonists von Merritt, J. Robert, James, Ray, Paradkar, Vidyadhar M., Zhang, Chongwu, Liu, Ruiyan, Liu, Jinqi, Jacob, Biji, Chiriac, Camelia, Ohlmeyer, Michael J., Quadros, Elizabeth, Wines, Pamela, Postelnek, Jennifer, Hicks, Catherine M., Chen, Weiqing, Kimble, Earl F., O’Brien, Linda, White, Nicole, Desai, Hema, Appell, Kenneth C., Webb, Maria L.

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Allosteric Inhibitors of Inducible Nitric Oxide Synthase Dimerization Discovered via Combinatorial Chemistry von McMillan, Kirk, Adler, Marc, Auld, Douglas S., Baldwin, John J., Blasko, Eric, Browne, Leslie J., Chelsky, Daniel, Davey, David, Dolle, Ronald E., Eagen, Keith A., Erickson, Shawn, Feldman, Richard I., Glaser, Charles B., Mallari, Cornell, Morrissey, Michael M., Michael H. J. Ohlmeyer, Pan, Gonghua, Parkinson, John F., Phillips, Gary B., Polokoff, Mark A., Sigal, Nolan H., Vergona, Ronald, Whitlow, Marc, Young, Tish A., Devlin, James J.

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Complex Synthetic Chemical Libraries Indexed with Molecular Tags von Michael H. J. Ohlmeyer, Swanson, Robert N., Dillard, Lawrence W., Reader, John C., Asouline, Gigi, Kobayashi, Ryuji, Wigler, Michael, Still, W. Clark

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Synthesis and SAR studies of novel 2-(4-oxo-2-aryl-quinazolin-3(4H)-yl)acetamide vasopressin V₁b receptor antagonists von Napier, Susan E, Letourneau, Jeffrey J, Ansari, Nasrin, Auld, Douglas S, Baker, James, Best, Stuart, Campbell-Wan, Leigh, Chan, Jui-Hsiang, Craighead, Mark, Desai, Hema, Goan, Katharine A, Ho, Koc-Kan, Hulskotte, Ellen G.J, MacSweeney, Cliona P, Milne, Rachel, Morphy, J. Richard, Neagu, Irina, Ohlmeyer, Michael H.J, Peeters, Ard W.M.M, Presland, Jeremy, Riviello, Chris, Ruigt, Ge S.F, Thomson, Fiona J, Zanetakos, Heather A, Zhao, Jiuqiao, Webb, Maria L

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Synthesis and SAR studies of novel 2-(6-aminomethylaryl-2-aryl-4-oxo-quinazolin-3(4H)-yl)acetamide Vasopressin V₁b receptor antagonists von Napier, Susan E, Letourneau, Jeffrey J, Ansari, Nasrin, Auld, Douglas S, Baker, James, Best, Stuart, Campbell-Wan, Leigh, Chan, Ray, Craighead, Mark, Desai, Hema, Ho, Koc-Kan, MacSweeney, Cliona, Milne, Rachel, Richard Morphy, J, Neagu, Irina, Ohlmeyer, Michael H.J, Pick, Jack, Presland, Jeremy, Riviello, Chris, Zanetakos, Heather A, Zhao, Jiuqiao, Webb, Maria L

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Synthesis and initial evaluation of novel, non-peptidic antagonists of the alpha(v)-integrins alpha(v)beta(3) and alpha(v)beta(5) von Letourneau, Jeffrey J, Liu, Jinqi, Ohlmeyer, Michael H J, Riviello, Chris, Rong, Yajing, Li, Hong, Appell, Kenneth C, Bansal, Shalini, Jacob, Biji, Wong, Angela, Webb, Maria L

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Synthesis of a Small Molecule Combinatorial Library Encoded with Molecular Tags von Baldwin, John J, Burbaum, Jonathan J, Henderson, Ian, Ohlmeyer, Michael H. J

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Manipulation of substrate-controlled diastereoselectivities in hydroborations of acyclic allylamine derivatives von Burgess, Kevin, Ohlmeyer, Michael J

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A Paradigm for Drug Discovery Employing Encoded Combinatorial Libraries von Burbaum, Jonathan J., Michael H. J. Ohlmeyer, Reader, John C., Henderson, Ian, Dillard, Lawrence W., Li, Ge, Randle, Troy L., Sigal, Nolan H., Chelsky, Daniel, Baldwin, John J.

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Stereochemically matched (and mismatched) bisphosphine ligands: DIOP-DIPAMP hybrids von Burgess, Kevin, Ohlmeyer, Michael J, Whitmire, Kenton H

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Substrate-controlled diastereoselectivities in catalyzed and uncatalyzed hydroborations of acyclic allylic alcohol derivatives: secondary orbital effects involving d.pi.-p.pi. inte... von Burgess, Kevin, Cassidy, Juanita, Ohlmeyer, Michael J

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Further evidence for the role of d.pi.-p.pi. bonding in rhodium-mediated hydroborations von Burgess, Kevin, Van der Donk, Wilfred A, Jarstfer, Michael B, Ohlmeyer, Michael J

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Diastereocontrol in rhodium-catalyzed hydroboration of chiral acyclic allylic alcohol derivatives von Burgess, Kevin, Ohlmeyer, Michael J.

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Enantioselective hydroborations catalyzed by rhodium(+1) complexes von Burgess, Kevin, van der Donk, Wilfred A., Ohlmeyer, Michael J.

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