Reduction−Alkylation Strategies for the Modification of Specific Monoclonal Antibody Disulfides von Sun, Michael M. C, Beam, Kevin S, Cerveny, Charles G, Hamblett, Kevin J, Blackmore, Richard S, Torgov, Michael Y, Handley, Felicia G. M, Ihle, Nathan C, Senter, Peter D, Alley, Stephen C

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Nickel-catalyzed intramolecular [4 + 4]-cycloadditions: a new method for the synthesis of polycycles containing eight-membered rings von Wender, Paul A, Ihle, Nathan C

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Nickel-catalyzed intramolecular [4+4] cycloadditions. 4. Enantioselective total synthesis of (+)-asteriscanolide von Wender, Paul A, Ihle, Nathan C, Correia, Carlos R. D

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Nonpeptide αvβ3 antagonists. Part 2: Constrained glycyl amides derived from the RGD tripeptide von MEISSNER, Robert S, PERKINS, James J, RODAN, Gideon A, RODAN, Sevgi B, WHITMAN, David B, WESOLOWSKI, Gregg A, DUGGAN, Mark E, DUONG, Le T, HARTMAN, George D, HOFFMAN, William F, HUFF, Joel R, IHLE, Nathan C, LEU, Chih-Tai, NAGY, Rose M, NAYLOR-OLSEN, Adel

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Nicotinamide N-oxides as CXCR2 antagonists von CUTSHALL, Neil S, URSINO, Rocky, KUCERA, Kristin A, LATHAM, John, IHLE, Nathan C

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Non-Peptide Fibrinogen Receptor Antagonists. 7. Design and Synthesis of a Potent, Orally Active Fibrinogen Receptor Antagonist von Duggan, Mark E, Naylor-Olsen, Adel M, Perkins, James J, Anderson, Paul S, Chang, Charles T.-C, Cook, Jacquelynn J, Gould, Robert J, Ihle, Nathan C, Hartman, George D

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Palladium-catalyzed intramolecular alkyne-carbon monoxide-alkene insertion cascade for synthesis of .alpha.-methylenecyclopentenones von Ihle, Nathan C, Heathcock, Clayton H

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Nicotinanilides as inhibitors of neutrophil chemotaxis von Cutshall, Neil S., Kucera, Kristin A., Ursino, Rocky, Latham, John, Ihle, Nathan C.

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Stereochemical Assignments for All Four Isomers of Dolaproine via Lactam Formation von Shang, Xiao, Nguyen, Minh, Ihle, Nathan C.

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Preparation of 4-Alkyl-2-[N-(tert-butoxycarbonyl)amino]pyridines by Alkylation, Nucleophilic Addition, and Acylation of 2-[N-(tert-Butoxycarbonyl)amino]-4-picoline(1) von Ihle, Nathan C., Krause, Amy E.

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Preparation of 4-Alkyl-2-[N-(tert-butoxycarbonyl)amino]pyridines by Alkylation, Nucleophilic Addition, and Acylation of 2-[N-(tert-Butoxycarbonyl)amino]-4-picoline1 von Ihle, Nathan C, Krause, Amy E

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Nonpeptide αvβ3 Antagonists. 1. Transformation of a Potent, Integrin-Selective αIIbβ3 Antagonist into a Potent αvβ3 Antagonist von Duggan, Mark E, Duong, Le T, Fisher, John E, Hamill, Terence G, Hoffman, William F, Huff, Joel R, Ihle, Nathan C, Leu, Chih-Tai, Nagy, Rose M, Perkins, James J, Rodan, Sevgi B, Wesolowski, Gregg, Whitman, David B, Zartman, Amy E, Rodan, Gideon A, Hartman, George D

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Specific Tumor Targeting and Potent Bystander Killing with SGN-35, an Anti-CD30 Antibody Drug Conjugate von Okeley, Nicole M., Alley, Stephen C., Cerveny, Charles G., Andreyka, Jamie, Sanderson, Russell J., Anderson, Martha, Benjamin, Dennis R., Law, Che-Leung, Sievers, Eric, Ihle, Nathan C.

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Nonpeptide alpha(v)beta(3) antagonists. Part 2: constrained glycyl amides derived from the RGD tripeptide von Meissner, Robert S, Perkins, James J, Duong, Le T, Hartman, George D, Hoffman, William F, Huff, Joel R, Ihle, Nathan C, Leu, Chih Tai, Nagy, Rose M, Naylor-Olsen, Adel, Rodan, Gideon A, Rodan, Sevgi B, Whitman, David B, Wesolowski, Gregg A, Duggan, Mark E

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SGN-35, an Anti-CD30 Antibody-Drug Conjugate, Exhibits Potent Antitumor Activity for the Treatment of CD30+ Malignancies von Hamblett, Kevin J., Barton, Jeremy, Cerveny, Charles G., Andreyka, Jamie B., Kissler, Kim M., Okeley, Nicole M., Stone, Ivan, Sutherland, May K., Sun, Michael M., Senter, Peter D., Wahl, Alan F., Ihle, Nathan C.

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Preparation of 4-Alkyl-2-[ N -( tert -butoxycarbonyl)amino]pyridines by Alkylation, Nucleophilic Addition, and Acylation of 2-[ N -( tert -Butoxycarbonyl)amino]-4-picoline 1 von Ihle, Nathan C., Krause, Amy E.

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Nickel-catalyzed intramolecular [4+4] cycloadditions: 2. Allylic stereoinduction and modelling studies in the preparation of bicyclo[6.4.0]dodecadienes von Wender, Paul A., Ihle, Nathan C.

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Nonpeptide α vβ 3 antagonists. Part 2: constrained glycyl amides derived from the RGD tripeptide von Meissner, Robert S., Perkins, James J., Duong, Le T., Hartman, George D., Hoffman, William F., Huff, Joel R., Ihle, Nathan C., Leu, Chih-Tai, Nagy, Rose M., Naylor-Olsen, Adel, Rodan, Gideon A., Rodan, Sevgi B., Whitman, David B., Wesolowski, Gregg A., Duggan, Mark E.

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Nonpeptide α v β 3 Antagonists. 1. Transformation of a Potent, Integrin-Selective α IIb β 3 Antagonist into a Potent α v β 3 Antagonist von Duggan, Mark E., Duong, Le T., Fisher, John E., Hamill, Terence G., Hoffman, William F., Huff, Joel R., Ihle, Nathan C., Leu, Chih-Tai, Nagy, Rose M., Perkins, James J., Rodan, Sevgi B., Wesolowski, Gregg, Whitman, David B., Zartman, Amy E., Rodan, Gideon A., Hartman, George D.

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FIBRINOGEN-REZEPTOR-ANTAGONISTEN von DUGGAN, MARK E, IHLE, NATHAN C

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