Max Sarvestani

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Process Development of the BACE Inhibitors BI 1147560 BS and BI 1181181 MZ

Jinhua J. Song, S. Venkatraman, C. Senanayake, 2022, Organic Process Research & Development.

Development of a Safe and Economical Synthesis of Methyl 6-Chloro-5-(trifluoromethyl)nicotinate: Trifluoromethylation on Kilogram Scale

Jinhua J. Song, C. Senanayake, J. Mulder, 2013 .

Development of a large scale asymmetric synthesis of the glucocorticoid agonist BI 653048 BS H3PO4.

Jinhua J. Song, B. Narayanan, C. Senanayake, 2013, The Journal of organic chemistry.

PAT Application in the Expedited Development of a Three-Step, One-Stage Synthesis of the Dipeptide Intermediate of HCV Protease Inhibitor Faldaprevir

C. Senanayake, Heewon Lee, B. Qu, 2015 .

Development of a Practical Sequence for Difluoromethylation of 2‐Bromopyridines via Copper‐Mediated Reductive Coupling and Decarboxylation

Jinhua J. Song, C. Senanayake, Xudong Wei, 2015 .

A facile and practical synthesis of N-acetyl enamides.

C. Senanayake, Xudong Wei, N. Yee, 2009, The Journal of organic chemistry.

Copper-Catalyzed Asymmetric Propargylation of Cyclic Aldimines.

C. Senanayake, K. Fandrick, Daniel R Fandrick, 2016, Organic letters.

Synthesis of Enantioenriched 2-Alkyl Piperidine Derivatives through Asymmetric Reduction of Pyridinium Salts.

Jinhua J. Song, C. Senanayake, Xudong Wei, 2016, Organic letters.

A superior method for the reduction of secondary phosphine oxides.

Paul S. Sabila, C. Senanayake, Xudong Wei, 2005, Organic letters.

Safety Assessment of Benzyne Generation from a Silyl Triflate Precursor.

N. Garg, C. Busacca, I. Volchkov, 2020, Organic letters.

Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement

Jinhua J. Song, B. Narayanan, Bing-Shiou Yang, 2017 .

Development of a Pilot-Plant Process for a Nevirapine Analogue HIV NNRT Inhibitor

P. Beaulieu, Ji-Young Kim, D. Norwood, 2008 .

Practical Large‐Scale Synthesis of the Hepatitis C Virus Protease Inhibitor BI 201335

C. Senanayake, Xudong Wei, J. Smoliga, 2012 .

Formation of 2-Trifluoromethylphenyl Grignard Reagent via Magnesium−Halogen Exchange: Process Safety Evaluation and Concentration Effect

B. Narayanan, C. Senanayake, Xudong Wei, 2009 .

A scalable and regioselective synthesis of 2-difluoromethyl pyridines from commodity chemicals.

Jinhua J. Song, C. Senanayake, Xudong Wei, 2014, Organic letters.

Sulfone Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4-Quinolinyl Ethers and more - Application to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420.

B. Narayanan, C. Senanayake, Xudong Wei, 2020, The Journal of organic chemistry.

Process safety evaluation of a magnesium : Iodine exchange reaction

Jinhua J. Song, C. Senanayake, N. Yee, 2006 .

Synthesis of a Sodium–Hydrogen Exchange Type 1 Inhibitor: An Efficient Cu-Catalyzed Conjugated Addition of a Grignard Reagent to an Acetyl Pyridinium Salt

B. Narayanan, Bing-Shiou Yang, C. Senanayake, 2013 .

Large-scale asymmetric synthesis of a cathepsin S inhibitor.

C. Senanayake, Xudong Wei, Heewon Lee, 2010, The Journal of organic chemistry.

Development of a Scalable Synthesis toward a KRAS G12C Inhibitor Building Block Bearing an All-Carbon Quaternary Stereocenter, Part 1: From Discovery Route to Kilogram-Scale Production

Jinhua J. Song, Denis Byrne, Joe Johnson, 2024, Organic Process Research & Development.

Development of a Scalable Synthesis toward a KRAS G12C Inhibitor Building Block Bearing an All-Carbon Quaternary Stereocenter, Part 2: Asymmetric Synthesis via Shi Epoxidation

Jinhua J. Song, F. Buono, Jon C. Lorenz, 2024, Organic Process Research & Development.