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Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosides. The Journal of organic chemistry, 2013/06/07, Volume 78, Issue 11, p.5160-71, (2013)
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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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Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells. Bioorganic & medicinal chemistry letters, 2013/03/15, Volume 23, Issue 6, p.1834-8, (2013)
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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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Hits, leads and drugs against malaria through diversity-oriented synthesis. Future medicinal chemistry, 2012/12/01, Volume 4, Issue 18, p.2279-94, (2012)
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Identification of a selective small molecule inhibitor of breast cancer stem cells. Bioorganic & medicinal chemistry letters, 2012/05/15, Volume 22, Issue 10, p.3571-4, (2012)
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Overcoming fluconazole resistance in Candida albicans clinical isolates with tetracyclic indoles. Bioorganic & medicinal chemistry letters, 2012/05/01, Volume 22, Issue 9, p.3362-5, (2012)
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Development of small-molecule probes that selectively kill cells induced to express mutant RAS. Bioorganic & medicinal chemistry letters, 2012/02/15, Volume 22, Issue 4, p.1822-6, (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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Identification of small-molecule inhibitors of Trypansoma cruzi replication. Bioorganic & medicinal chemistry letters, 2011/12/01, Volume 21, Issue 23, p.7197-200, (2011)
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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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Piperazinyl quinolines as chemosensitizers to increase fluconazole susceptibility of Candida albicans clinical isolates. Bioorganic & medicinal chemistry letters, 2011/09/15, Volume 21, Issue 18, p.5502-5, (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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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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- Showing 1-23 of 23 Results




