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An informatic pipeline for managing high-throughput screening experiments and analyzing data from stereochemically diverse libraries. Journal of computer-aided molecular design, 2013/04/13, (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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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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Diversity-Oriented Synthesis Yields a Novel Lead for the Treatment of Malaria. ACS medicinal chemistry letters, 2012/02/09, Volume 3, Issue 2, p.112-117, (2012)
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Application of natural product-inspired diversity-oriented synthesis to drug discovery. Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques, 2012/01/05, Volume 66, p.187, 189-216, (2012)
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Diversity-oriented synthesis of 13- to 18-membered macrolactams via ring-closing metathesis. The Journal of organic chemistry, 2011/10/07, Volume 76, Issue 19, p.8042-8, (2011)
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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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Practical asymmetric synthesis of β-hydroxy γ-amino acids via complimentary aldol reactions. Tetrahedron, 2011/08/26, Volume 67, Issue 34, p.6131-6137, (2011)
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Application of a sparse matrix design strategy to the synthesis of dos libraries. ACS combinatorial science, 2011/07/11, Volume 13, Issue 4, p.357-64, (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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Fragment-based domain shuffling approach for the synthesis of pyran-based macrocycles. Proceedings of the National Academy of Sciences of the United States of America, 2011/04/26, Volume 108, Issue 17, p.6751-6, (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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Grand challenge commentary: Accessing new chemical space for 'undruggable' targets. Nature chemical biology, 2010/12/01, Volume 6, Issue 12, p.861-3, (2010)
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Current strategies for diversity-oriented synthesis. Current opinion in chemical biology, 2010/06/01, Volume 14, Issue 3, p.362-70, (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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Identifying the proteins to which small-molecule probes and drugs bind in cells. Proceedings of the National Academy of Sciences of the United States of America, 2009/03/24, Volume 106, Issue 12, p.4617-22, (2009)
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Large scale preparation of silicon-functionalized SynPhase Polystyrene lanterns for solid-phase synthesis. Journal of combinatorial chemistry, 1969/12/31, Volume 11, Issue 1, p.110-6, (1969)
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