Total Synthesis of (+)-Fawcettimine von Linghu, Xin, Kennedy-Smith, Joshua J, Toste, F. Dean

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Gold(I)-Catalyzed Cyclizations of Silyl Enol Ethers: Application to the Synthesis of (+)-Lycopladine A von Staben, Steven T., Kennedy-Smith, Joshua J., Huang, David, Corkey, Britton K., LaLonde, Rebecca L., Toste, F. Dean

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Gold(I)-Catalyzed 5-endo-dig Carbocyclization of Acetylenic Dicarbonyl Compounds von Staben, Steven T., Kennedy-Smith, Joshua J., Toste, F. Dean

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Enantioselective Reduction of Ketones and Imines Catalyzed by (CN-Box)ReV-Oxo Complexes von Nolin, Kristine A., Ahn, Richard W., Kobayashi, Yusuke, Kennedy-Smith, Joshua J., Toste, F. Dean

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Total Synthesis of (−)-Heptemerone B and (−)-Guanacastepene E von Miller, Aubry K, Hughes, Chambers C, Kennedy-Smith, Joshua J, Gradl, Stefan N, Trauner, Dirk

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Diphenyl Ether Non-Nucleoside Reverse Transcriptase Inhibitors with Excellent Potency Against Resistant Mutant Viruses and Promising Pharmacokinetic Properties von Sweeney, Zachary K., Kennedy-Smith, Joshua J., Wu, Jeffrey, Arora, Nidhi, Billedeau, J. Roland, Davidson, James P., Fretland, Jennifer, Hang, Julie Q., Heilek, Gabrielle M., Harris, Seth F., Hirschfeld, Donald, Inbar, Petra, Javanbakht, Hassan, Jernelius, Jesper A., Jin, Qingwu, Li, Yu, Liang, Weiling, Roetz, Ralf, Sarma, Keshab, Smith, Mark, Stefanidis, Dimitrio, Su, Guoping, Suh, Judy M., Villaseñor, Armando G., Welch, Michael, Zhang, Fang-Jie, Klumpp, Klaus

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Potent and selective TYK2-JH1 inhibitors highly efficacious in rodent model of psoriasis von Leit, Silvana, Greenwood, Jeremy R., Mondal, Sayan, Carriero, Samantha, Dahlgren, Markus, Harriman, Geraldine C., Kennedy-Smith, Joshua J., Kapeller, Rosana, Lawson, Jon P., Romero, Donna L., Toms, Angela V., Shelley, Mee, Wester, Ronald T., Westlin, William, McElwee, Joshua J., Miao, Wenyan, Edmondson, Scott D., Masse, Craig E.

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Gold(I)-Catalyzed Conia-Ene Reaction of β-Ketoesters with Alkynes von Kennedy-Smith, Joshua J, Staben, Steven T, Toste, F. Dean

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Enantioselective reduction of ketones and imines catalyzed by (CN-box)Re(V)-oxo complexes von Nolin, Kristine A, Ahn, Richard W, Kobayashi, Yusuke, Kennedy-Smith, Joshua J, Toste, F Dean

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Rational Design of a Chiral Palladium(0) Olefin Complex of Unprecedented Stability von Grundl, Marc A, Kennedy-Smith, Joshua J, Trauner, Dirk

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Rhenium-Catalyzed Aromatic Propargylation von Kennedy-Smith, Joshua J, Young, Lauren A, Toste, F. Dean

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Pyrrolopyrazines as Selective Spleen Tyrosine Kinase Inhibitors von Padilla, Fernando, Bhagirath, Niala, Chen, Shaoqing, Chiao, Eric, Goldstein, David M, Hermann, Johannes C, Hsu, Jonathan, Kennedy-Smith, Joshua J, Kuglstatter, Andreas, Liao, Cheng, Liu, Wenjian, Lowrie, Lee E, Luk, Kin Chun, Lynch, Stephen M, Menke, John, Niu, Linghao, Owens, Timothy D, O-Yang, Counde, Railkar, Aruna, Schoenfeld, Ryan C, Slade, Michelle, Steiner, Sandra, Tan, Yun-Chou, Villaseñor, Armando G, Wang, Ce, Wanner, Jutta, Xie, Wenwei, Xu, Daigen, Zhang, Xiaohu, Zhou, Mingyan, Lucas, Matthew C

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Using Ovality to Predict Nonmutagenic, Orally Efficacious Pyridazine Amides as Cell Specific Spleen Tyrosine Kinase Inhibitors von Lucas, Matthew C, Bhagirath, Niala, Chiao, Eric, Goldstein, David M, Hermann, Johannes C, Hsu, Pei-Yuan, Kirchner, Stephan, Kennedy-Smith, Joshua J, Kuglstatter, Andreas, Lukacs, Christine, Menke, John, Niu, Linghao, Padilla, Fernando, Peng, Ying, Polonchuk, Liudmila, Railkar, Aruna, Slade, Michelle, Soth, Michael, Xu, Daigen, Yadava, Preeti, Yee, Calvin, Zhou, Mingyan, Liao, Cheng

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Reversing the Role of the Metal−Oxygen π-Bond. Chemoselective Catalytic Reductions with a Rhenium(V)-Dioxo Complex von Kennedy-Smith, Joshua J, Nolin, Kristine A, Gunterman, Haluna P, Toste, F. Dean

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Design of Annulated Pyrazoles as Inhibitors of HIV-1 Reverse Transcriptase von Sweeney, Zachary K, Harris, Seth F, Arora, Nidhi, Javanbakht, Hassan, Li, Yu, Fretland, Jennifer, Davidson, James P, Billedeau, J. Roland, Gleason, Shelley K, Hirschfeld, Donald, Kennedy-Smith, Joshua J, Mirzadegan, Taraneh, Roetz, Ralf, Smith, Mark, Sperry, Sarah, Suh, Judy M, Wu, Jeffrey, Tsing, Stan, Villaseñor, Armando G, Paul, Amber, Su, Guoping, Heilek, Gabrielle, Hang, Julie Q, Zhou, Amy S, Jernelius, Jesper A, Zhang, Fang-Jie, Klumpp, Klaus

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Synthetic Studies toward the Guanacastepenes von Hughes, Chambers C, Kennedy-Smith, Joshua J, Trauner, Dirk

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Synthesis and biological activity of new pyridone diaryl ether non-nucleoside inhibitors of HIV-1 reverse transcriptase von Kennedy-Smith, Joshua J., Arora, Nidhi, Billedeau, J. Roland, Fretland, Jennifer, Hang, Julie Q., Heilek, Gabrielle M., Harris, Seth F., Hirschfeld, Donald, Javanbakht, Hassan, Li, Yu, Liang, Weiling, Roetz, Ralf, Smith, Mark, Su, Guoping, Suh, Judy M., Villaseñor, Armando G., Wu, Jeffrey, Yasuda, Dennis, Klumpp, Klaus, Sweeney, Zachary K.

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Gold(I)-Catalyzed Cyclizations of Silyl Enol Ethers: Application to the Synthesis of (+)-Lycopladine A von Staben, Steven T., Kennedy-Smith, Joshua J., Huang, David, Corkey, Britton K., LaLonde, Rebecca L., Toste, F. Dean

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A Practical Variant of the Claisen-Eschenmoser Rearrangement: Synthesis of Unsaturated Morpholine Amides von Gradl, Stefan N., Kennedy-Smith, Joshua J., Kim, James, Trauner, Dirk

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Cover Picture: Diphenyl Ether Non-Nucleoside Reverse Transcriptase Inhibitors with Excellent Potency Against Resistant Mutant Viruses and Promising Pharmacokinetic Properties (Chem... von Sweeney, Zachary K., Kennedy-Smith, Joshua J., Wu, Jeffrey, Arora, Nidhi, Billedeau, J. Roland, Davidson, James P., Fretland, Jennifer, Hang, Julie Q., Heilek, Gabrielle M., Harris, Seth F., Hirschfeld, Donald, Inbar, Petra, Javanbakht, Hassan, Jernelius, Jesper A., Jin, Qingwu, Li, Yu, Liang, Weiling, Roetz, Ralf, Sarma, Keshab, Smith, Mark, Stefanidis, Dimitrio, Su, Guoping, Suh, Judy M., Villaseñor, Armando G., Welch, Michael, Zhang, Fang-Jie, Klumpp, Klaus

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