Z. Song

发表

Synthesis of Verubecestat, a BACE1 Inhibitor for the Treatment of Alzheimer's Disease.

Steven P. Miller, L. Tan, A. Lekhal, 2016, Organic letters.

Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase Inhibitor.

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

Synthesis of bis-macrocyclic HCV protease inhibitor MK-6325 via intramolecular sp²-sp³ Suzuki-Miyaura coupling and ring closing metathesis.

Jeremy P. Scott, L. Tan, Cheng-yi Chen, 2015, Organic letters.

Synthesis of vaniprevir (MK-7009): lactamization to prepare a 20-membered [corrected] macrocycle.

Paul N. Devine, D. Tellers, D. Zewge, 2011, The Journal of organic chemistry.

Practical Asymmetric Synthesis of a Calcitonin Gene-Related Peptide (CGRP) Receptor Antagonist Ubrogepant

Weng Lin Tang, L. Tan, F. Cabirol, 2017 .

Asymmetric Formal Synthesis of the Long-Acting DPP-4 Inhibitor Omarigliptin.

L. Tan, E. Sherer, Yonggang Chen, 2017, The Journal of organic chemistry.

Enantioselective hydrogenation of an α-alkoxy substituted ketone with chiral ruthenium (phosphinoferrocenyl)oxazoline complexes

D. Tellers, Yong-kui Sun, J. McWilliams, 2006 .

Practical Synthesis of A Macrocyclic HCV Protease Inhibitor: A High-Yielding Macrolactam Formation

Paul N. Devine, D. Tellers, D. Zewge, 2014 .

Diverse Catalytic Reactions for the Stereoselective Synthesis of Cyclic Dinucleotide MK-1454.

Andrew J. Neel, Ben W. H. Turnbull, L. Tan, 2022, 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.

Enantioselective Synthesis of 4'-Ethynyl-2-fluoro-2'-deoxyadenosine (EFdA) via Enzymatic Desymmetrization.

D. Murray, L. Tan, Jeffrey C. Moore, 2017, Organic letters.

Asymmetric Synthesis of Letermovir Using a Novel Phase-Transfer-Catalyzed Aza-Michael Reaction

G. Humphrey, S. M. Dalby, Z. Song, 2016 .

Preparation of 1‐Methoxy‐2‐(4‐Methoxyphenoxy)Benzene

Z. Song, Elizabeth Buck, 2005 .

Oxidation of Primary Alcohols to Carboxylic Acids with Sodium Chlorite Catalyzed by TEMPO and Bleach

P. Reider, E. Grabowski, Z. Song, 1999 .

A practical chemoenzymatic synthesis of an LTD4 antagonist

P. Reider, E. Grabowski, D. Hughes, 1993 .

Synthesis of Bridged Bicyclic Amines by Intramolecular Amination of Remote C-H Bonds: Synergistic Activation by Light and Heat.

R. Sarpong, D. Adpressa, C. Yeung, 2020, Organic letters.

Carbon‐14 labeling of a potential new immunoregulant agent

D. Dean, D. Melillo, Z. Song, 2000 .

Oxetane Promise Delivered: Discovery of Long-Acting IDO1 Inhibitors Suitable for Q3W Oral or Parenteral Dosing.

Theodore A. Martinot, Yongxin Han, N. Solban, 2022, Journal of medicinal chemistry.

Ullmann diaryl ether synthesis: rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione.

R. Volante, P. Reider, Z. Song, 2002, Organic letters.

A Unified Strategy to Fluorinated Nucleoside Analogues Via an Electrophilic Manifold.

Andrew J. Neel, Ben W. H. Turnbull, L. Tan, 2022, Organic letters.

Oxidation of Primary Alcohols to Carboxylic Acids with Sodium Chlorite Catalyzed by TEMPO and Bleach: 4‐Methoxyphenylacetic Acid

Z. Song, D. Tschaen, E. Mano, 2005 .

A novel chromium trioxide catalyzed oxidation of primary alcohols to the carboxylic acids

P. Reider, E. Grabowski, Z. Song, 1998 .

Development of Scalable Routes to 1-Bicyclo[1.1.1]pentylpyrazoles

Michael J. Ardolino, Matthew L. Maddess, Kaitlyn M. Logan, 2020 .

Pd-Catalyzed Cyanation of a Bromoaryl Carboxylate En Route to Etrumadenant: Robust Process with Low Catalyst Loading Enabled by Preactivation

Z. Song, J. Hartung, Xiang Wang, 2022, Organic Process Research & Development.

Practical Asymmetric Synthesis of an Endothelin Receptor Antagonist

Paul N. Devine, R. Volante, P. Reider, 1999 .

Enantioselective preparation of ring-fused 1-fluorocyclopropane-1-carboxylate derivatives: en route to mGluR 2 receptor agonist MGS0028.

R. Volante, Z. Song, D. Tschaen, 2004, Organic letters.

Preparation of 2-(2H-Tetrazol-2-yl)benzoic Acids via Regioselective Cu(I) Catalyzed N2 Arylation of Tetrazole

Yonggang Chen, G. Humphrey, P. Maligres, 2019, Organic Process Research & Development.

Efficient synthesis of NK(1) receptor antagonist aprepitant using a crystallization-induced diastereoselective transformation.

Jing Li, Paul N Devine, Paul N. Devine, 2003, Journal of the American Chemical Society.

Asymmetric Synthesis of Functionalized trans-Cyclopropoxy Building Block for Grazoprevir.

Rebecca T. Ruck, M. Truppo, Hongming Li, 2017, Organic letters.

SERM: Selective Estrogen Receptor Modulator

Z. Song, 2010 .

Rhodium-carbenoid-mediated intermolecular O–H insertion reactions: a dramatic additive effect. Application in the synthesis of an ascomycin derivative

P. Reider, Martha Huntington, E. Grabowski, 2000 .

A stereoselective aldol reaction via diisopinocampheyl boron-enolate in preparation of chromane carboxylate with quaternary carbon

D. Zewge, R. Volante, P. Reider, 2003 .

An Efficient Synthesis of an NMDA Receptor Antagonist via Stereoselective Fluorination

M. Waters, Z. Song, M. Bio, 2008 .

A Publication of Reliable Methods for the Preparation of Organic Compounds

Z. Song, D. Tschaen, E. Mano, 2016 .

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.

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 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 .

Practical synthesis of a potent hepatitis C virus RNA replication inhibitor.

R. Volante, E. Grabowski, Feng Xu, 2004, The Journal of organic chemistry.

Improved synthesis of quinaldines by the skraup reaction

M. Mertzman, D. Hughes, Z. Song, 1993 .

Process Safety Considerations for the Supply of a High-Energy Oxadiazole IDO1-Selective Inhibitor

Lu Chen, Theodore A. Martinot, Michael J. Ardolino, 2019, Organic Process Research & Development.

Practical asymmetric synthesis of aprepitant, a potent human NK-1 receptor antagonist, via a stereoselective Lewis acid-catalyzed trans acetalization reaction.

P. Reider, E. Grabowski, Guojie Ho, 2002, The Journal of organic chemistry.

Development of a Kilogram-Scale Synthesis of a Key Ulevostinag Subunit Part I: Accessing a Keto-Nucleoside Intermediate from Guanosine

Andrew J. Neel, Ben W. H. Turnbull, L. Tan, 2023, Organic Process Research & Development.

An improved synthesis of N-isocyanoiminotriphenylphosphorane and its use in the preparation of diazoketones

Z. Song, M. Bio, Gary J Javadi, 2004 .

A Practical Chemoenzymatic Synthesis of an LTD4 Antagonist.

P. Reider, E. Grabowski, D. Hughes, 1993 .

Two Scalable Syntheses of 3-(Trifluoromethyl)cyclobutane-1-carboxylic Acid

M. Emmert, J. Qi, Z. Song, 2021 .

Concise Cu (I) Catalyzed Synthesis of Substituted Benzofurans via a Tandem SNAr/C–O Coupling Process

L. Tan, Z. Song, Guiquan Liu, 2016 .

An efficient asymmetric synthesis of an estrogen receptor modulator by sulfoxide-directed borane reduction.

D. Zewge, D. Mathre, R. Volante, 2004, Proceedings of the National Academy of Sciences of the United States of America.