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Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione

Organic letters, 2002-05, Vol.4 (9), p.1623-1626

2002

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Selective Synthesis of N 6 ,3′,5′-Tripivaloyladenosine via Dynamic Kinetic Crystallization and Regioselective Preparation of Pivalated 2′-Deoxy-2′-fluoroarabinoadenosines

Organic process research & development, 2024-10

2024

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Development of a Concise Process for the Synthesis of the Azaindazole Core of the CD73 Inhibitor AB680

Organic process research & development, 2023-05, Vol.27 (5), p.945-953

2023

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

Organic process research & development, 2022-11, Vol.26 (11), p.3161-3165

2022

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

Organic process research & development, 2019-11, Vol.23 (11), p.2354-2361

2019

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

Organic process research & development, 2016-06, Vol.20 (6), p.1097-1103

2016

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A Unified Strategy to Fluorinated Nucleoside Analogues Via an Electrophilic Manifold

Organic letters, 2022-10, Vol.24 (41), p.7701-7706

2022

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

Organic process research & development, 2021-03, Vol.25 (3), p.642-647

2021

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

Organic process research & development, 2023-03, Vol.27 (3), p.448-457

2023

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Synthesis of Fused Oxepane HIV Integrase Inhibitor MK-1376

Synthesis (Stuttgart), 2020-11, Vol.52 (22), p.3378-3388

2020

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Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods

Chemical science (Cambridge), 2021-07, Vol.12 (26), p.931-936

2021

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

Organic process research & development, 2022-09, Vol.26 (9), p.2728-2738

2022

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

Journal of the American Chemical Society, 2022-04, Vol.144 (13), p.5855-5863

2022

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Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase Inhibitor

Journal of organic chemistry, 2019-04, Vol.84 (8), p.4780-4795

2019

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

Tetrahedron letters, 2000-03, Vol.41 (12), p.1877-1881

2000

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Synthesis of Bis-Macrocyclic HCV Protease Inhibitor MK-6325 via Intramolecular sp 2–sp 3 Suzuki–Miyaura Coupling and Ring Closing Metathesis

Organic letters, 2015-03, Vol.17 (6), p.1533-1536

2015

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An Efficient Synthesis of an NMDA Receptor Antagonist via Stereoselective Fluorination

Synthesis (Stuttgart), 2008-03, Vol.2008 (6), p.891-896

2008

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An Improved Synthesis of N-Isocyanoiminotriphenylphosphorane and Its Use in the Preparation of Diazoketones

Synthesis (Stuttgart), 2005-01, Vol.2005 (1), p.19-21

2005

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Enantioselective Synthesis of 1,4-Dihydrobenzoxathiins via Sulfoxide-Directed Borane Reduction

Synthesis (Stuttgart), 2006-10, Vol.2006 (20), p.3389-3396

2006

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

Organic letters, 2015-03, Vol.17 (6), p.1533-1536

2015

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ChemInform Abstract: SERM: Selective Estrogen Receptor Modulator

ChemInform, 2011-12, Vol.42 (51), p.no-no

Song, Zhiguo Jake

2011

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SERM: Selective Estrogen Receptor Modulator

The Art of Process Chemistry, 2010, p.143-164

2010

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An Improved Synthesis of N-Isocyanoiminotriphenylphosphorane and Its Use in the Preparation of Diazoketones

ChemInform, 2005-05, Vol.36 (21), p.no-no

2005

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Enantioselective Synthesis of 1,4-Dihydrobenzoxathiins via Sulfoxide-Directed Borane Reduction

ChemInform, 2007-03, Vol.38 (12), p.no-no

2007

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Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione

ChemInform, 2002-09, Vol.33 (38), p.76-76

2002

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Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione

Selective Synthesis of N 6 ,3′,5′-Tripivaloyladenosine via Dynamic Kinetic Crystallization and Regioselective Preparation of Pivalated 2′-Deoxy-2′-fluoroarabinoadenosines

Development of a Concise Process for the Synthesis of the Azaindazole Core of the CD73 Inhibitor AB680

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

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

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

A Unified Strategy to Fluorinated Nucleoside Analogues Via an Electrophilic Manifold

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

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

Synthesis of Fused Oxepane HIV Integrase Inhibitor MK-1376

Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods

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

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

Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase Inhibitor

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

Synthesis of Bis-Macrocyclic HCV Protease Inhibitor MK-6325 via Intramolecular sp 2–sp 3 Suzuki–Miyaura Coupling and Ring Closing Metathesis

An Efficient Synthesis of an NMDA Receptor Antagonist via Stereoselective Fluorination

An Improved Synthesis of N-Isocyanoiminotriphenylphosphorane and Its Use in the Preparation of Diazoketones

Enantioselective Synthesis of 1,4-Dihydrobenzoxathiins via Sulfoxide-Directed Borane Reduction

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

ChemInform Abstract: SERM: Selective Estrogen Receptor Modulator

SERM: Selective Estrogen Receptor Modulator

An Improved Synthesis of N-Isocyanoiminotriphenylphosphorane and Its Use in the Preparation of Diazoketones

Enantioselective Synthesis of 1,4-Dihydrobenzoxathiins via Sulfoxide-Directed Borane Reduction

Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione

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