Fuh-Rong Tsay

发表

Stereoselective synthesis of an anti-HIV drug candidate.

M. Palucki, D. Conlon, D. Hughes, 2005, Chirality.

Generic anion-exchange chromatography method for analytical and preparative separation of nucleotides in the development and manufacture of drug substances.

E. Regalado, I. Mangion, A. Makarov, 2019, Journal of chromatography. A.

Synthesis of 3-aminopyrazinone mediated by 2-pyridylthioimidate-ZnCl2 complexes. Development of an efficient route to a thrombin inhibitor.

D. Mathre, John Y. L. Chung, Jennifer R. Chilenski, 2003, The Journal of organic chemistry.

An improved preparation of 3,5-bis(trifluoromethyl)acetophenone and safety considerations in the preparation of 3,5-bis(trifluoromethyl)phenyl Grignard reagent.

Donald C. Bachert, R. Cvetovich, J. Leazer, 2003, The Journal of organic chemistry.

Practical synthesis of the new carbapenem antibiotic ertapenem sodium.

D. Sidler, T. Novak, R. Skerlj, 2005, The Journal of organic chemistry.

Development of a new and practical route to chiral 3,4-disubstituted cyclopentanones: asymmetric alkylation and intramolecular cyclopropanation as key C-C bond-forming steps.

M. Palucki, P. Reider, D. Conlon, 2002, The Journal of organic chemistry.

Synthesis of Mavatrep: A Potent Antagonist of Transient Receptor Potential Vanilloid-1

R. Russell, A. Abdel-Magid, C. Teleha, 2015 .

An Efficient Synthesis of a Dual PPAR α/γ Agonist and the Formation of a Sterically Congested α-Aryloxyisobutyric Acid via a Bargellini Reaction

John Y. L. Chung, R. Cvetovich, J. Amato, 2005 .

Highly Chemoselective Trichloroacetimidate-Mediated Alkylation of Ascomycin: A Convergent, Practical Synthesis of the Immunosuppressant L-733,725.

Yulan Li, D. Mathre, P. Reider, 1999, The Journal of organic chemistry.

A Highly Efficient Synthesis of Fibrinogen Receptor Antagonist L-734,217 via a Novel Chemoselective Silyl-Mediated Conjugate Addition of δ-Lactams to 4-Vinylpyridine

A. W. Douglas, D. Mathre, P. Reider, 1996 .

A kinase-cGAS cascade to synthesize a therapeutic STING activator

Steven P. Miller, Paul N. Devine, Matthew L. Maddess, 2022, Nature.

Assignment of the 1H and 13C NMR spectra of 1-methyl-6-phenyl-1α,4α,4aα,5α,8β,8aα-hexahydro-1,4-methanonaphthalene-5,8-diol

A. P. Marchand, D. Minter, Fuh-Rong Tsay, 2003 .

Practical Synthesis of Anti-Methicillin-Resistant Staphylococcus Aureus (MRSA) Carbapenem L-742,728

A. W. Douglas, Yulan Li, D. Mathre, 1998 .

Mapping the Separation Landscape of Pharmaceuticals: Rapid and Efficient Scale-Up of Preparative Purifications Enabled by Computer-Assisted Chromatographic Method Development

Jimmy O. DaSilva, Raffeal Bennett, Imad A. Haidar Ahmad, 2019, Organic Process Research & Development.

Automated ion exchange chromatography screening combined with in silico multifactorial simulation for efficient method development and purification of biopharmaceutical targets

Jimmy O. DaSilva, D. Guillarme, E. Regalado, 2022, Analytical and Bioanalytical Chemistry.

Understanding the Origin of Unusual Stepwise Hydrogenation Kinetics in the Synthesis of the 3-(4-Fluorophenyl)morpholine Moiety of NK1 Receptor Antagonist Aprepitant

Shane W. Krska, E. Corley, R. Reamer, 2006 .

Synthesis of a Complex and Highly Potent PCSK9 Inhibitor.

Jimmy O. DaSilva, Jeffrey T. Kuethe, E. Regalado, 2023, Organic letters.