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A Potent and Selective Quinoxalinone-Based STK33 Inhibitor Does Not Show Synthetic Lethality in KRAS-Dependent Cells. ACS medicinal chemistry letters, 2012/12/13, Volume 3, Issue 12, p.1034-1038, (2012)
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Synthesis and Profiling of a Diverse Collection of Azetidine-Based Scaffolds for the Development of CNS-Focused Lead-like Libraries. The Journal of organic chemistry, 2012/08/10, (2012)
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Build/Couple/Pair Strategy for the Synthesis of Stereochemically Diverse Macrolactams via Head-to-Tail Cyclization. ACS combinatorial science, 2012/02/13, Volume 14, Issue 2, p.89-96, (2012)
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Synthesis of a stereochemically diverse library of medium-sized lactams and sultams via S(N)Ar cycloetherification. ACS combinatorial science, 2011/07/11, Volume 13, Issue 4, p.365-74, (2011)
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An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors. Journal of the American Chemical Society, 2010/12/01, Volume 132, Issue 47, p.16962-76, (2010)
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Accessing skeletal diversity using catalyst control: formation of n and n + 1 macrocyclic triazole rings. Organic letters, 2009/06/04, Volume 11, Issue 11, p.2257-60, (2009)
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Diastereoselective synthesis of gamma-lactams by a one-pot, four-component reaction. Organic letters, 2007/09/27, Volume 9, Issue 20, p.4077-80, (2007)
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