Search Results - "McCabe Dunn, Jamie M."
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Total Synthesis of Darobactin A
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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Mechanistic Understanding of a Robust and Scalable Synthesis of Per(6-deoxy-6-halo)cyclodextrins, Versatile Intermediates for Cyclodextrin Modification
Published in Organic process research & development (19-03-2021)“…Cyclodextrin (CD) perfunctionalization reactions are challenging to study because they proceed through a number of regioisomeric intermediates, thus warranting…”
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Development of a Palladium-Catalyzed α‑Arylation of Cyclopropyl Nitriles
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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The protecting-group free selective 3'-functionalization of nucleosides
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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The Safe Use of Sodium Hydride on Scale: The Process Development of a Chloropyrimidine Displacement
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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Rapid End-Game Process Development and First GMP Production of MK-7845: An Experimental Antiviral Treatment for COVID-19
Published in Organic process research & development (21-06-2024)“…We describe the rapid end-game process development for the first good manufacturing process (GMP) delivery of the 3C-like protease inhibitor MK-7845 (1), an…”
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The protecting-group free selective 3′-functionalization of nucleosidesElectronic supplementary information (ESI) available. CCDC 1525736-1525737. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc05081f
Published 28-03-2017“…The direct and chemoselective 3′-phosphoramidation, phosphorylation and acylation of nucleosides are described. Upon the discovery of a novel…”
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The protecting-group free selective 3′-functionalization of nucleosides† †Electronic supplementary information (ESI) available. CCDC 1525736–1525737. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc05081f Click here for additional data file. Click here for additional data file
Published in Chemical science (Cambridge) (18-01-2017)“…The direct and chemoselective 3′-phosphoramidation, phosphorylation and acylation of nucleosides are described. The direct and chemoselective…”
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