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John Limanto

Merck & Co.

13

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280

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Kilogram-Scale Synthesis of 2′-C-Methyl-arabino-Uridine from Uridine via Dynamic Selective Dipivaloylation

2021 Organic Process Research & Development
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Improved Process for a Copper-Catalyzed C–NCoupling in the Synthesis of Verubecestat

2019 Organic Process Research & Development
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Multi-column Ultra-high Performance Liquid Chromatography Screening with Chaotropic Agents and Computer-assisted Separation Modeling Enables Process Development of New Drug Substances

2019 Analyst
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Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase Inhibitor

2019 Journal of Organic Chemistry
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Supercritical fluid chromatography-photodiode array detection-electrospray ionization mass spectrometry as a framework for impurity fate mapping in the development and manufacture of drug substances

2018 Journal of Chromatography B
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A multifunctional catalyst that stereoselectively assembles prodrugs

2017 Science
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Practical and Cost-Effective Manufacturing Route for the Synthesis of a β-Lactamase Inhibitor

2014 Organic Letters
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Dynamic Kinetic Resolution: Asymmetric Transfer Hydrogenation of α-Alkyl-Substituted β-Ketoamides.

2010 ChemInform
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Dynamic Kinetic Resolution: Asymmetric Transfer Hydrogenation of α-Alkyl-Substituted β-Ketoamides

2010 Organic Letters
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Non-Cryogenic CeCl3-Promoted Double Additions of Methyllithium and n-Butyllithium to Unsaturated Nitriles

2006 Synthesis
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