Identification of potent and selective retinoic acid receptor gamma (RARγ) antagonists for the treatment of osteoarthritis pain using structure based drug design by Hughes, Norman E., Bleisch, Thomas J., Jones, Scott A., Richardson, Timothy I., Doti, Robert A., Wang, Yong, Stout, Stephanie L., Durst, Gregory L., Chambers, Mark G., Oskins, Jennifer L., Lin, Chaohua, Adams, Lisa A., Page, Todd J., Barr, Robert J., Zink, Richard W., Osborne, Harold, Montrose-Rafizadeh, Chahrzad, Norman, Bryan H.

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Design and synthesis of a novel series of [1-(4-hydroxy-benzyl)-1H-indol-5-yloxy]-acetic acid compounds as potent, selective, thyroid hormone receptor β agonists by Burkholder, Timothy P., Cunningham, Brian E., Clayton, Joshua R., Lander, Peter A., Brown, Matthew L., Doti, Robert A., Durst, Gregory L., Montrose-Rafizadeh, Chahrzad, King, Constance, Osborne, Harold E., Amos, Robert M., Zink, Richard W., Stramm, Lawrence E., Burris, Thomas P., Cardona, Guemalli, Konkol, Debra L., Reidy, Charles, Christe, Michael E., Genin, Michael J.

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3,3-Bisaryloxindoles as mineralocorticoid receptor antagonists by Neel, David A., Brown, Matthew L., Lander, Peter A., Grese, Timothy A., Defauw, Jean M., Doti, Robert A., Fields, Todd, Kelley, Sally Ann, Smith, Stephon, Zimmerman, Karen M., Steinberg, Mitchell I., Jadhav, Prabhakar K.

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Identification of potent and selective retinoic acid receptor gamma (RARγ) antagonists for the treatment of osteoarthritis pain using structure based drug design by Hughes, Norman E., Bleisch, Thomas J., Jones, Scott A., Richardson, Timothy I., Doti, Robert A., Wang, Yong, Stout, Stephanie L., Durst, Gregory L., Chambers, Mark G., Oskins, Jennifer L., Lin, Chaohua, Adams, Lisa A., Page, Todd J., Barr, Robert J., Zink, Richard W., Osborne, Harold, Montrose-Rafizadeh, Chahrzad, Norman, Bryan H.

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Discovery of Potent, Selective, and Orally Active Carboxylic Acid Based Inhibitors of Matrix Metalloproteinase-13 by Monovich, Lauren G, Tommasi, Ruben A, Fujimoto, Roger A, Blancuzzi, Vincent, Clark, Kirk, Cornell, Wendy D, Doti, Robert, Doughty, John, Fang, James, Farley, David, Fitt, John, Ganu, Vishwas, Goldberg, Ronald, Goldstein, Robert, Lavoie, Stacey, Kulathila, Raviraj, Macchia, William, Parker, David T, Melton, Richard, O’Byrne, Elizabeth, Pastor, Gary, Pellas, Theodore, Quadros, Elizabeth, Reel, Noela, Roland, Dennis M, Sakane, Yumi, Singh, Hem, Skiles, Jerry, Somers, Joseph, Toscano, Karen, Wigg, Andrew, Zhou, Siyuan, Zhu, Lijuan, Shieh, Wen-Chung, Xue, Song, McQuire, Leslie W

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Simultaneous determination of enantiomeric purity and erythro/ threo relationship in chiral 1,2-aminoalcohols by NMR using ( R)-(+)- t-butylphenylphosphinothioic acid by Gunderson, Karl G, Shapiro, Michael J, Doti, Robert A, Skiles, Jerry W

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Carboxy-Substituted Cinnamides:  A Novel Series of Potent, Orally Active LTB4 Receptor Antagonists by Greenspan, Paul D, Fujimoto, Roger A, Marshall, Paul J, Raychaudhuri, Anil, Lipson, Kenneth E, Zhou, Huanghai, Doti, Robert A, Coppa, David E, Zhu, Lijuan, Pelletier, Roberta, Uziel-Fusi, Susan, Jackson, Robert H, Chin, Michael H, Kotyuk, Bernard L, Fitt, John J

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N-aryl cinnamides : A novel class of rigid and highly potent leukotriene B4 receptor antagonists by GREENSPAN, P. D, MAIN, A. J, JACKSON, R. H, UZIEL-FUSI, S, BHAGWAT, S. S, BARSKY, L. I, DOTI, R. A, ENGLE, A. R, FREY, L. M, ZHOU, H, LIPSON, K. E, CHIN, M. H

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Carboxy-Substituted Cinnamides:  A Novel Series of Potent, Orally Active LTB 4 Receptor Antagonists by Greenspan, Paul D., Fujimoto, Roger A., Marshall, Paul J., Raychaudhuri, Anil, Lipson, Kenneth E., Zhou, Huanghai, Doti, Robert A., Coppa, David E., Zhu, Lijuan, Pelletier, Roberta, Uziel-Fusi, Susan, Jackson, Robert H., Chin, Michael H., Kotyuk, Bernard L., Fitt, John J.

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N-aryl cinnamides: A novel class of rigid and highly potent leukotriene B 4 receptor antagonists by Greenspan, Paul D., Main, Alan J., Bhagwat, Shripad S., Barsky, Lester I., Doti, Robert A., Engle, Alan R., Frey, Lisa M., Zhou, Huanghai, Lipson, Kenneth E., Chin, Michael H., Jackson, Robert H., Uziel-Fusi, Susan

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Synthesis with HOCl: conversion of pulegone and isopulegol to menthofuran: preparation of 3,6-dimethyl-2,6-cycloheptadien-1-one from phorone by HEGDE, S. G, BECKWITH, D, DOTI, R, WOLINSKY, J

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Synthesis with hypochlorous acid. Conversion to pulegone and isopulegol to menthofuran. Preparation of 3,6-dimethyl-2,6-cycloheptadien-1-one from phorone by Hegde, Shridhar G, Beckwith, David, Doti, Robert, Wolinsky, Joseph

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