alpha.-Alkylation and stereochemistry of cis- and trans-decahydroquinolines mediated by the formamidine and Boc activating groups. Synthesis of pumiliotoxin C von Meyers, A. I, Milot, Guy

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Pyridoxine hydroxamic acids as novel HIV-integrase inhibitors von Stranix, Brent R., Wu, Jinzi J., Milot, Guy, Beaulieu, Françis, Bouchard, Jean-Emanuel, Gouveia, Kristine, Forte, André, Garde, Seema, Wang, Zhigang, Mouscadet, Jean-François, Delelis, Olivier, Xiao, Yong

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Regioselectivity in forming dipole-stabilized anions. Sites of metalation of indolines, tetrahydroquinolines, and benzazepines activated by N-formimidoyl or N-Boc groups von Meyers, A. I, Milot, Guy

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Structure-Based Design of Potent, Amidine-Derived Inhibitors of Factor Xa:  Evaluation of Selectivity, Anticoagulant Activity, and Antithrombotic Activity von Wiley, Michael R, Weir, Leonard C, Briggs, Steven, Bryan, Nancy A, Buben, John, Campbell, Charles, Chirgadze, Nickolay Y, Conrad, Richard C, Craft, Trelia J, Ficorilli, James V, Franciskovich, Jeffry B, Froelich, Larry L, Gifford-Moore, Donetta S, Goodson, Theodore, Herron, David K, Klimkowski, Valentine J, Kurz, Kenneth D, Kyle, Jeffery A, Masters, John J, Ratz, Andrew M, Milot, Guy, Shuman, Robert T, Smith, Tommy, Smith, Gerald F, Tebbe, Ann Louise, Tinsley, Jennifer M, Towner, Richard D, Wilson, Alexander, Yee, Ying K

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The design and synthesis of substituted biphenyl libraries von Pavia, Michael R., Cohen, Michael P., Dilley, Garrett J., Dubuc, Gloria R., Durgin, Tracy L., Forman, Frank W., Hediger, Mark E., Milot, Guy, Powers, Timothy S., Sucholeiki, Irving, Zhou, Shulan, Hangauer, David G.

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Rearrangements and stereochemistry of S2 additions to olefins von STELIOU, K, GAREAU, Y, MILOT, G, SALAMA, P

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LYSME-BASED PRODRUGS OF ASPARTYL PROTEASE INHIBITORS AND PROCESSES FOR THEIR PREPARATION von STRANIX, BRENT, RICHARD, MILOT, GUY, BRANCHAUD, STEPHANE

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Lysine-based prodrugs of aspartyl protease inhibitors and processes for their preparation von MILOT GUY, BRANCHAUD STEPHANE, STRANIX BRENT R

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A reinvestigation of the reported synthesis of the spirobenzyl isoquinoline alkaloid, iso-ochotensine von Meyers, A.I, Akahane, Atsushi, Struzka, Vladimir, Warmus, Joseph S, Gonzalez, Michael, Milot, Guy

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DERIVATIVES OF PYRIDOXINE FOR INHIBITING HIV INTEGRASE von BOUCHARD, JEAN-EMMANUEL, STRANIX, BRENT, MILOT, GUY

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DERIVATIVES OF PYRIDOXINE FOR INHIBITING HIV INTEGRASE von BOUCHARD, JEAN-EMMANUEL, STRANIX, BRENT, MILOT, GUY

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Lysine-based prodrugs of aspartyl protease inhibitors and processes for their preparation von MILOT GUY, BRANCHAUD STEPHANE, STRANIX BRENT R

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Lysine-based prodrugs of aspartyl protease inhibitors and processes for their preparation von Milot, Guy, Branchaud, Stephane, Stranix, Brent R

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1,2-Dibenzamidobenzene Inhibitors of Human Factor Xa von Herron, David K, Goodson, Theodore, Wiley, Michael R, Weir, Leonard C, Kyle, Jeffrey A, Yee, Ying K, Tebbe, Ann Louise, Tinsley, Jennifer M, Mendel, David, Masters, John J, Franciskovich, Jeffry B, Sawyer, J. Scott, Beight, Douglas W, Ratz, Andrew M, Milot, Guy, Hall, Steven E, Klimkowski, Valentine J, Wikel, James H, Eastwood, Brian J, Towner, Richard D, Gifford-Moore, Donetta S, Craft, Trelia J, Smith, Gerald F

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Lysine-based prodrugs of aspartyl protease inhibitors and processes for their preparation von MILOT, GUY, BRANCHAUD, STEPHANE, STRANIX, BRENT RICHARD

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Derivatives of pyridoxine for inhibiting HIV integrase von STRANIX BRENT RICHARD, BOUCHARD JEAN-EMMANUEL, MILOT GUY

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PROTEASE INHIBITORS von STRANIX, Brent Richard, LAVALLEE, Jean-Francois, LEBERRE, Nicolas, HERBART, Dominik, MILOT, Guy, PANCHAL, Chandra J, PERRON, Valerie

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DERIVATIVES OF PYRIDOXINE FOR INHIBITING HIV INTEGRASE von BOUCHARD, JEAN-EMMANUEL, STRANIX, BRENT, MILOT, GUY

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LYSME-BASED PRODRUGS OF ASPARTYL PROTEASE INHIBITORS AND PROCESSES FOR THEIR PREPARATION von STRANIX, BRENT, RICHARD, MILOT, GUY, BRANCHAUD, STEPHANE

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Synthesis of chiral 2,6-dithiabicyclo[3.1.1]heptane. The dithia parent analog of the TXA2 nucleus von Steliou, Kosta, Milot, Guy

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