J. Limanto

发表

Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase Inhibitor.

L. Tan, E. Sherer, Hongming Li, 2018, The Journal of organic chemistry.

An Efficient Chemoenzymatic Approach to (S)-γ-Fluoroleucine Ethyl Ester

Paul N. Devine, R. Volante, R. Reamer, 2005 .

Intramolecular cycloadditions of cyclobutadiene with olefins.

K. Houk, J. Tallarico, Kelli S. Khuong, 2002, Journal of the American Chemical Society.

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

Timothy J. Wright, Tyler A. Davis, Louis-Charles Campeau, 2021, Organic Process Research & Development.

Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods†

Timothy J. Wright, Rebecca T. Ruck, Tyler A. Davis, 2021, Chemical science.

Process Development of C−N Cross-Coupling and Enantioselective Biocatalytic Reactions for the Asymmetric Synthesis of Niraparib

Guy R. Humphrey, Mark E. Scott, Kevin M. Belyk, 2014 .

Synthesis of the GPR40 Partial Agonist MK-8666 through a Kinetically Controlled Dynamic Enzymatic Ketone Reduction.

Nicholas J Agard, L. Tan, Eric Ashley, 2016, Organic letters.

Non-cryogenic CeCl3-promoted double additions of methyllithium and n-butyllithium to unsaturated nitriles

Paul N. Devine, J. Limanto, B. Dorner, 2006 .

Dynamic kinetic resolution: asymmetric transfer hydrogenation of alpha-alkyl-substituted beta-ketoamides.

L. Tan, S. Krska, Enrique Vazquez, 2010, Organic letters.

A multifunctional catalyst that stereoselectively assembles prodrugs

Yining Ji, Louis-Charles Campeau, Rebecca T. Ruck, 2017, Science.

Promotion of a Ti-Mediated Mannich Reaction by a Proton Source.

L. Tan, R. Reamer, A. Brunskill, 2016, The Journal of organic chemistry.

Dynamic Kinetic Resolution: Asymmetric Transfer Hydrogenation of α‐Alkyl‐Substituted β‐Ketoamides.

L. Tan, S. Krska, Enrique Vazquez, 2010 .

Synthesis of a tertiary carbinamide via a novel Rh-catalyzed asymmetric hydrogenation.

Paul N. Devine, S. Krska, J. Limanto, 2008, The Journal of organic chemistry.

An Efficient Approach to 3-Bromo-6-chloro-phenanthrene-9,10-dione

L. Tan, F. W. Hartner, J. Limanto, 2008 .

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.

Robert Hartman, Artis Klapars, E. Regalado, 2018, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Practical and cost-effective manufacturing route for the synthesis of a β-lactamase inhibitor.

Steven P. Miller, Y. Zhong, N. Yasuda, 2014, Organic letters.

Manufacturing Process Development for Uprifosbuvir (MK-3682): A Green and Sustainable Process for Preparing Penultimate 2′-Deoxy-α-2′-Chloro-β-2′-Methyluridine

Michael A. Zompa, Rebecca T. Ruck, George Zhou, 2022, Organic Process Research & Development.

A regioselective approach to 5-substituted-3-amino-1,2,4-triazines.

Paul N. Devine, R. Volante, R. Reamer, 2003, Organic letters.

Intramolecular cycloadditions of cyclobutadiene with dienes: experimental and computational studies of the competing (2 + 2) and (4 + 2) modes of reaction.

K. Houk, Kelli S. Khuong, M. Snapper, 2003, Journal of the American Chemical Society.

A highly efficient asymmetric synthesis of vernakalant.

M. Truppo, Eric Ashley, G. Beutner, 2014, Organic letters.

Multi-column ultra-high performance liquid chromatography screening with chaotropic agents and computer-assisted separation modeling enables process development of new drug substances.

E. Regalado, I. Mangion, Timothy Nowak, 2019, The Analyst.