Rapid Synthesis of Aryl Fluorides in Continuous Flow through the Balz-Schiemann Reaction von Park, Nathaniel H., Senter, Timothy J., Buchwald, Stephen L.

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Enantioselective Total Synthesis of (+)-Amabiline von Senter, Timothy J, Fadeyi, Olugbeminiyi O, Lindsley, Craig W

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Electrochemically Enabled Chan–Lam Couplings of Aryl Boronic Acids and Anilines von Wexler, Ryan P, Nuhant, Philippe, Senter, Timothy J, Gale-Day, Zachary J

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High-Affinity Small-Molecule Inhibitors of the Menin-Mixed Lineage Leukemia (MLL) Interaction Closely Mimic a Natural Protein–Protein Interaction von He, Shihan, Senter, Timothy J, Pollock, Jonathan, Han, Changho, Upadhyay, Sunil Kumar, Purohit, Trupta, Gogliotti, Rocco D, Lindsley, Craig W, Cierpicki, Tomasz, Stauffer, Shaun R, Grembecka, Jolanta

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Discovery and Optimization of Pyrazole Amides as Inhibitors of ELOVL1 von Come, Jon H, Senter, Timothy J, Clark, Michael P, Court, John J, Gale-Day, Zachary, Gu, Wenxin, Krueger, Elaine, Liang, Jianglin, Morris, Mark, Nanthakumar, Suganthini, O’Dowd, Hardwin, Maltais, Francois, Iyer, Ganesh, Andreassi, John, Boucher, Christina, Considine, Tony, Moody, Cameron S, Taylor, William, Mohanty, Arun K, Huang, Yulin, Zuccola, Harmon, Coll, Joyce, Bonanno, Kenneth C, Gagnon, Kevin J, Gan, Lu, Lu, Fan, Gao, Hong, Chakilam, Ananthisrinivas, Engtrakul, Juntyma, Song, Bin, Crawford, Dan, Doyle, Elisabeth, Kramer, Tal, Vought, Bryan, Phillips, Jonathan, Kemper, Raymond, Sanders, Martin, Swett, Rebecca, Furey, Brinley, Winquist, Ray, Bunnage, Mark E, Jackson, Katrina L, Charifson, Paul S, Magavi, Sanjay S

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A Versatile Enantioselective Synthesis of Azabicyclic Ring Systems: A Concise Total Synthesis of (+)-Grandisine D and Unnatural Analogues von Fadeyi, Olugbeminiyi O., Senter, Timothy J., Hahn, Kristopher N., Lindsley, Craig W.

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A general, enantioselective synthesis of N-alkyl terminal aziridines and C2-functionalized azetidines via organocatalysis von Senter, Timothy J., O’Reilly, Matthew C., Chong, Katherine M., Sulikowski, Gary A., Lindsley, Craig W.

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A general, enantioselective synthesis of 1-azabicyclo[m.n.0]alkane ring systems von Senter, Timothy J., Schulte, Michael L., Konkol, Leah C., Wadzinski, Tyler E., Lindsley, Craig W.

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Rapid Synthesis of Aryl Fluorides in Continuous Flow through the Balz-Schiemann Reaction von Park, Nathaniel H., Senter, Timothy J., Buchwald, Stephen L.

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APOL1 Inhibitors Reverse Established Proteinuria in an APOL1-Mediated Kidney Disease Mouse Model: TH-PO442 von Blasio, Angelo, Sullivan, Kelly E., Mann, James J., Wang, Guanyu, Kumar, Shyamesh, Bright, Franklin, Bouillez, Audrey, Daniel, Kevin, Nanthakumar, Suganthini, Rosario, Aldo A., Aragon Mejia, Monica A., Heighton, Thomas F., Nanou, Evanthia, Proctor, Jennifer, Furey, Brinley, Fortier, Anne, Senter, Timothy J., Dakin, Leslie, Zimmerman, Brandon

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A series of substituted isoindolinones as selective small molecule modulators of the Gβγ‐SNARE interaction von Zurawski, Zack P, Temple, Kayla Jo, Han, Changho, Delbove, Claire, Senter, Timothy J, Hyde, Karren, Lindsley, Craig W, Zhang, Qi, Stauffer, Shaun R, Hamm, Heidi E

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A Versatile Enantioselective Synthesis of Azabicyclic Ring Systems: A Concise Total Synthesis of (+)-GrandisineD and Unnatural Analogues von Fadeyi, Olugbeminiyi O, Senter, Timothy J, Hahn, Kristopher N, Lindsley, Craig W

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High-Affinity Small-Molecule Inhibitors of the Menin-Mixed Lineage Leukemia (MLL) Interaction Closely Mimic a Natural Protein–Protein Interaction von He, Shihan, Senter, Timothy J., Pollock, Jonathan, Han, Changho, Upadhyay, Sunil Kumar, Purohit, Trupta, Gogliotti, Rocco D., Lindsley, Craig W., Cierpicki, Tomasz, Stauffer, Shaun R., Grembecka, Jolanta

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Abstract 2534: High-affinity small molecule inhibitors of the menin-MLL interaction reverse oncogenic transformation mediated by MLL fusion proteins in leukemia von Grembecka, Jolanta E., He, Shihan, Senter, Timothy J., Borkin, Dmitry, Pollock, Jonathan, Han, Changho, Upadhyay, Sunil Kumar, Purohit, Trupta, Miao, Hongzhi, Gogliotti, Rocco D. Gogliotti D., Lindsley, Craig W., Cierpicki, Tomasz, Stauffer, Shaun R.

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ChemInform Abstract: A General, Enantioselective Synthesis of N-Alkyl Terminal Aziridines and C2-Functionalized Azetidines via Organocatalysis von Senter, Timothy J., O'Reilly, Matthew C., Chong, Katherine M., Sulikowski, Gary A., Lindsley, Craig W.

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ChemInform Abstract: A General, Enantioselective Synthesis of 1-Azabicyclo[m.n.0]alkane Ring Systems von Senter, Timothy J., Schulte, Michael L., Konkol, Leah C., Wadzinski, Tyler E., Lindsley, Craig W.

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SPIROCYCLIC INHIBITORS OF APOL1 AND METHODS OF USING SAME von DOLGIKH, Elena, SENTER, Timothy J, WANG, Haoxuan, CHEN, Ming, STONE, Steven D, OLSEN, Jessica H, DAKIN, Leslie A

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2-METHYL-4-PHENYLPIPERIDIN-4-OL DERIVATIVES AS INHIBITORS OF APOL1 AND METHODS OF USING SAME von DOLGIKH, Elena, SENTER, Timothy J, OLSEN, Jessica H, STONE, Steven D, DAKIN, Leslie A, SHIMIZU, Akira J

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SPIROCYCLIC INHIBITORS OF APOL1 AND METHODS OF USING SAME von DOLGIKH, Elena, SENTER, Timothy J, WANG, Haoxuan, CHEN, Ming, STONE, Steven D, OLSEN, Jessica H, DAKIN, Leslie A

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SPIRO PIPERIDINE DERIVATIVES AS INHIBITORS OF APOL1 AND METHODS OF USING SAME von WANG, Tiansheng, SENTER, Timothy J, NAMIREMBE, Sheila, WANG, Haoxuan, CHEN, Ming, GALE-DAY, Zachary, OLSEN, Jessica H, DAKIN, Leslie A, SHIMIZU, Akira J

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