Development of an Efficient Synthesis of the Pyrrolquinolone PHA-529311 von Dorow, R. L, Herrinton, Paul M, Hohler, Richard A, Maloney, Mark T, Mauragis, Michael A, McGhee, William E, Moeslein, Jeffery A, Strohbach, Joseph W, Veley, Michael F

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Evolution of the Synthesis of AMPK Activators for the Treatment of Diabetic Nephropathy: From Three Preclinical Candidates to the Investigational New Drug PF-06409577 von Smith, Aaron C, Kung, Daniel W, Shavnya, Andre, Brandt, Thomas A, Dent, Philip D, Genung, Nathan E, Cabral, Shawn, Panteleev, Jane, Herr, Michael, Yip, Ka Ning, Aspnes, Gary E, Conn, Edward L, Dowling, Matthew S, Edmonds, David J, Edmonds, Ian D, Fernando, Dilinie P, Herrinton, Paul M, Keene, Nandell F, Lavergne, Sophie Y, Li, Qifang, Polivkova, Jana, Rose, Colin R, Thuma, Benjamin A, Vetelino, Michael G, Wang, Guoqiang, Weaver, John D, Widlicka, Daniel W, Price Wiglesworth, Kristin E, Xiao, Jun, Zahn, Todd, Zhang, Yingxin

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Solvent and in situ catalyst preparation impacts upon Noyori reductions of aryl-chloromethyl ketones: application to syntheses of chiral 2-amino-1-aryl-ethanols von Tanis, Steven P., Evans, Bruce R., Nieman, James A., Parker, Timothy T., Taylor, Wendy D., Heasley, Steven E., Herrinton, Paul M., Perrault, William R., Hohler, Richard A., Dolak, Lester A., Hester, Matthew R., Seest, Eric P.

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Synthesis of 3-acyltetrahydrofurans from formaldehyde acetals of allylic diols von Gasparski, Catherine M, Herrinton, Paul M, Overman, Larry E, Wolfe, John P

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Iodination and Metal Halogen Exchange of Aromatic Compounds:  An Improved Preparation of a Key Oxazolidinone Antibiotic Intermediate von Herrinton, Paul M, Owen, Carolyn E, Gage, James R

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Oxidation and alkylation of spectinomycin derivatives: synthesis of trospectomycin from spectinomycin von Herrinton, Paul M, Klotz, Karen L, Hartley, William M

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Furans in synthesis. 3. Furans as terminators in cationic cyclization von Tanis, Steven P, Herrinton, Paul M

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Acid-promoted reaction of cyclic allylic diols with carbonyl compounds. Stereoselective ring-enlarging tetrahydrofuran annulations von Brown, Mark J, Harrison, Timothy, Herrinton, Paul M, Hopkins, Mark H, Hutchinson, Kira D, Overman, Larry E, Mishra, Pratibha

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Comparison of Commercially Available Reagents for Fluorination of Steroid 3,5-Dienol Acetates von Reydellet-Casey, Valérie, Knoechel, Donald J, Herrinton, Paul M

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The Synthesis of N-Aryl-5(S)-aminomethyl-2-oxazolidinone Antibacterials and Derivatives in One Step from Aryl Carbamates von Perrault, William R., Pearlman, Bruce A., Godrej, Delara B., Jeganathan, Azhwarsamy, Yamagata, Koji, Chen, Jiong J., Lu, Cuong V., Herrinton, Paul M., Gadwood, Robert C., Chan, Lai, Lyster, Mark A., Maloney, Mark T., Moeslein, Jeffery A., Greene, Meredith L., Barbachyn, Michael R.

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Furans in synthesis. 5. Furan-terminated cationic cyclizations in the preparation of fused, spirocyclic and bridged ring systems. An application to the synthesis of nakafuran 9 von Tanis, Steven P, Herrinton, Paul M

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Preparation of alpha, beta-unsaturated enones von HERRINTON, PAUL M

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A convenient synthesis of vinyl spiro epoxides from .alpha.,.beta.-unsaturated ketones von Tanis, Steven P., McMills, Mark C., Herrinton, Paul M.

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Oxidative preparation of 3,5-secoandrost-5-one-3,17 beta -dioic acid von HERRINTON, PAUL M

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Protected derivatives of the enone of spectinomycin von HERRINTON, PAUL M

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Furans in Synthesis. The Preparation of Spiro-Cyclic Systems von Tanis, Steven P., Herrinton, Paul M., Dixon, Lisa A.

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Oxidative Preparation of 3,5-Secoandrost-5-One-3,17Beta-Dioic Acid von HERRINTON, PAUL M

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ChemInform Abstract: Iodination and Metal Halogen Exchange of Aromatic Compounds: An Improved Preparation of a Key Oxazolidinone Antibiotic Intermediate von Herrinton, Paul M., Owen, Carolyn E., Gage, James R.

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3-(4-amidopyrrol-2-ylmethylidene)-2-indolinone derivatives as protein kinase inhibitors von Guan, Huiping, Liang, Congxin, Sun, Li, Tang, Peng Cho, Wei, Chung Chen, Vojkovsky, Tomas, Jin, Qingwu, Herrinton, Paul M, Mauragis, Michael A

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3-(4-amidopyrrol-2-ylmethylidene)-2-indolinone derivatives as protein kinase inhibitors von LIANG CONGXIN, GUAN HUIPING, WEI CHUNG CHEN, VOJKOVSKY TOMAS, SUN LI, JIN QINGWU, MAURAGIS MICHAEL A, HERRINTON PAUL M, TANG PENG CHO

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