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Synthesis of Stereochemically and Skeletally Diverse Fused Ring Systems from Functionalized C-Glycosides. The Journal of organic chemistry, 2013/05/21, (2013)
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Application of a Catalytic Asymmetric Povarov Reaction using Chiral Ureas to the Synthesis of a Tetrahydroquinoline Library. ACS combinatorial science, 2012/10/22, (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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Synthesis of a novel suppressor of beta-cell apoptosis via diversity-oriented synthesis. ACS medicinal chemistry letters, 2011/09/08, Volume 2, Issue 9, p.698-702, (2011)
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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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Large-scale synthesis of all stereoisomers of a 2,3-unsaturated C-glycoside scaffold. The Journal of organic chemistry, 2011/03/18, Volume 76, Issue 6, p.1898-901, (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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