Search Results - "McCabe Dunn, Jamie M."

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    Total Synthesis of Darobactin A by Nesic, Marko, Ryffel, David B., Maturano, Jonathan, Shevlin, Michael, Pollack, Scott R., Gauthier, Donald R., Trigo-Mouriño, Pablo, Zhang, Li-Kang, Schultz, Danielle M., McCabe Dunn, Jamie M., Campeau, Louis-Charles, Patel, Niki R., Petrone, David A., Sarlah, David

    Published in Journal of the American Chemical Society (10-08-2022)
    “…The collaborative total synthesis of darobactin A, a recently isolated antibiotic that selectively targets Gram-negative bacteria, has been accomplished in a…”
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    Journal Article
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    Development of a Palladium-Catalyzed α‑Arylation of Cyclopropyl Nitriles by McCabe Dunn, Jamie M., Kuethe, Jeffrey T., Orr, Robert K., Tudge, Matthew, Campeau, Louis-Charles

    Published in Organic letters (19-12-2014)
    “…1,1-Disubstituted aryl cyclopropyl nitriles are useful moieties in biologically active compounds and provide access to a range of cyclopropyl derivatives…”
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    Journal Article
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    The protecting-group free selective 3'-functionalization of nucleosides by McCabe Dunn, Jamie M, Reibarkh, Mikhail, Sherer, Edward C, Orr, Robert K, Ruck, Rebecca T, Simmons, Bryon, Bellomo, Ana

    Published in Chemical science (Cambridge) (01-04-2017)
    “…The direct and chemoselective 3'-phosphoramidation, phosphorylation and acylation of nucleosides are described. Upon the discovery of a novel…”
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    Journal Article
  5. 5

    The Safe Use of Sodium Hydride on Scale: The Process Development of a Chloropyrimidine Displacement by McCabe Dunn, Jamie M., Duran-Capece, Alicia, Meehan, Brendan, Ulis, James, Iwama, Tetsuo, Gloor, Guy, Wong, George, Bekos, Evan

    Published in Organic process research & development (18-11-2011)
    “…Sodium hydride was found to be the best base for a displacement reaction on a chloropyrimidine. Due to the insolubility of sodium hydride in all solvents and…”
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    Journal Article
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