Enantioselective Total Synthesis of Borrelidin von Duffey, Matthew O., LeTiran, Arnaud, Morken, James P.

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Rhodium-Catalyzed Enantioselective Reductive Aldol Reaction von Taylor, Steven J, Duffey, Matthew O, Morken, James P

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Total Syntheses of the Assigned Structures of Lituarines B and C von Smith, Amos B, Duffey, Matthew O, Basu, Kallol, Walsh, Shawn P, Suennemann, Hans W, Frohn, Michael

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Discovery and optimization of N-acyl and N-aroylpyrazolines as B-Raf kinase inhibitors von Blackburn, Christopher, Duffey, Matthew O., Gould, Alexandra E., Kulkarni, Bheemashankar, Liu, Jane X., Menon, Saurabh, Nagayoshi, Masayuki, Vos, Tricia J., Williams, Juliet

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Enantio- and Diastereoselective Reductive Aldol Reactions with Iridium-Pybox Catalysts von Zhao, Cun-Xiang, Duffey, Matthew O, Taylor, Steven J, Morken, James P

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Discovery of a Potent and Orally Bioavailable Benzolactam-Derived Inhibitor of Polo-Like Kinase 1 (MLN0905) von Duffey, Matthew O, Vos, Tricia J, Adams, Ruth, Alley, Jennifer, Anthony, Justin, Barrett, Cynthia, Bharathan, Indu, Bowman, Douglas, Bump, Nancy J, Chau, Ryan, Cullis, Courtney, Driscoll, Denise L, Elder, Amy, Forsyth, Nancy, Frazer, Jonathan, Guo, Jianping, Guo, Luyi, Hyer, Marc L, Janowick, David, Kulkarni, Bheemashankar, Lai, Su-Jen, Lasky, Kerri, Li, Gang, Li, Jing, Liao, Debra, Little, Jeremy, Peng, Bo, Qian, Mark G, Reynolds, Dominic J, Rezaei, Mansoureh, Scott, Margaret Porter, Sells, Todd B, Shinde, Vaishali, Shi, Qiuju Judy, Sintchak, Michael D, Soucy, Francois, Sprott, Kevin T, Stroud, Stephen G, Nestor, Michelle, Visiers, Irache, Weatherhead, Gabriel, Ye, Yingchun, D’Amore, Natalie

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Design and Optimization of Potent and Orally Bioavailable Tetrahydronaphthalene Raf Inhibitors von Gould, Alexandra E, Adams, Ruth, Adhikari, Sharmila, Aertgeerts, Kathleen, Afroze, Roushan, Blackburn, Christopher, Calderwood, Emily F, Chau, Ryan, Chouitar, Jouhara, Duffey, Matthew O, England, Dylan B, Farrer, Cheryl, Forsyth, Nancy, Garcia, Khristofer, Gaulin, Jeffery, Greenspan, Paul D, Guo, Ribo, Harrison, Sean J, Huang, Shih-Chung, Iartchouk, Natalia, Janowick, Dave, Kim, Mi-Sook, Kulkarni, Bheemashankar, Langston, Steven P, Liu, Jane X, Ma, Li-Ting, Menon, Saurabh, Mizutani, Hirotake, Paske, Erin, Renou, Christelle C, Rezaei, Mansoureh, Rowland, R. Scott, Sintchak, Michael D, Smith, Michael D, Stroud, Stephen G, Tregay, Ming, Tian, Yuan, Veiby, Ole P, Vos, Tricia J, Vyskocil, Stepan, Williams, Juliet, Xu, Tianlin, Yang, Johnny J, Yano, Jason, Zeng, Hongbo, Zhang, Dong Mei, Zhang, Qin, Galvin, Katherine M

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Discovery and optimization of pyrazoline compounds as B-Raf inhibitors von Duffey, Matthew O., Adams, Ruth, Blackburn, Christopher, Chau, Ryan W., Chen, Susan, Galvin, Katherine M., Garcia, Khristofer, Gould, Alexandra E., Greenspan, Paul D., Harrison, Sean, Huang, Shih-Chung, Kim, Mi-Sook, Kulkarni, Bheemashankar, Langston, Steven, Liu, Jane X., Ma, Li-Ting, Menon, Saurabh, Nagayoshi, Masayuki, Rowland, R. Scott, Vos, Tricia J., Xu, Tianlin, Yang, Johnny J., Yu, Shaoxia, Zhang, Qin

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Diversity-Oriented Synthesis of Polyketide Natural Products via Iterative Chemo- and Stereoselective Functionalization of Polyenoates:  Development of a Unified Approach for the C(... von Smith, Amos B, Walsh, Shawn P, Frohn, Michael, Duffey, Matthew O

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Simple Metal Alkoxides as Effective Catalysts for the Hetero-Aldol−Tishchenko Reaction von Mascarenhas, Cheryl M, Duffey, Matthew O, Liu, Shih-Yuan, Morken, James P

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Enantioselective Total Synthesis of Borrelidin  [J. Am. Chem. Soc. 2003, 125, 1458−1459]. von Duffey, Matthew O, LeTiran, Arnaud, Morken, James P

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Abstract 3573: A small molecule PLK1 inhibitor, MLN0905, yields broad anti-tumor activity in human xenograft tumor models, and synergizes with taxane therapy von Lasky, Kerri, Shi, Judy, Shinde, Vaishali, Stringer, Bradley, Qian, Mark G., Liao, Debra, Liu, Ray, Duffey, Matthew O., Vos, Tricia J., D'Amore, Natalie, Hyer, Marc, Rao, Youlan

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Bifunctional Molecular Linchpins: A Three-Component Coupling Protocol Employing 2-Bromoallyltrimethylsilane von Smith III, Amos B., Duffey, Matthew O.

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ENTIDADE QUÍMICA, COMPOSIÇÃO FARMACÊUTICA E SEU USO von DYLAN B. ENGLAND, MATTHEW O. DUFFEY, KOJI ONO, HIROTAKE MIZUTANI, HE XU, SCOTT FREEZE, ZHIGEN HU, CHARLES MCINTYRE, STEVEN LANGSTON

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entidade química, composição farmacêutica e seu uso von DYLAN B. ENGLAND, MATTHEW O. DUFFEY, KOJI ONO, HE XU, HIROTAKE MIZUTANI, CHARLES MCINTYRE, SCOTT FREEZE, ZHIGEN HU, STEVEN LANGSTON

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compostos de heteroarila, seus usos e composições farmacêuticas von DYLAN B. ENGLAND, MATTHEW O. DUFFEY, HE XU, HIROTAKE MIZUTANI, MITSUHIRO ITO, STEVEN P. LANGSTON, CHARLES MCINTYRE, ZHIGEN HU

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Heteroaryl compounds useful as inhibitors of sumo activating enzyme von Freeze, Scott, Hu, Zhigen, Xu, He, Langston, Steven, Ono, Koji, Duffey, Matthew O, England, Dylan, Mcintyre, Charles, Mizutani, Hirotake

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COMPUESTOS DE HETEROARILO UTILES COMO INHIBIDORES DE ENZIMA ACTIVADORA DE SUMO von ONO, Koji, DUFFEY, Matthew O, LANGSTON, Steven P, FREEZE, Scott, XU, He, ENGLAND, Dylan, MCINTYRE, Charles, MIZUTANI, Hirotake, HU, Zhigen

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COMPUESTOS DE HETEROARILO ÚTILES COMO INHIBIDORES DE ENZIMA ACTIVADORA DE SUMO von DUFFEY, Matthew, O, ONO, Koji, LANGSTON, Steven, P, FREEZE, Scott, XU, He, ENGLAND, Dylan, MCINTYRE, Charles, MIZUTANI, Hirotake, HU, Zhigen

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COMPUESTOS DE HETEROARILO ÚTILES COMO INHIBIDORES DE ENZIMA ACTIVADORA DE SUMO von MATTHEW O. DUFFEY, STEVEN P. LANDGSTON, KOJI ONO, HIROTAKE MIZUTANI, HE XU, DYLAN ENGLAND, SCOTT FREEZE, ZHIGEN HU, CHARLES MCINTYRE

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