Maxime C Soumeillant

发表

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 7. Development of a Regioselective Ullmann–Goldberg–Buchwald Reaction

Martin D. Eastgate, D. Blackmond, R. J. Fox, 2017 .

Synthesis of the 6-azaindole containing HIV-1 attachment inhibitor pro-drug, BMS-663068.

Martin D. Eastgate, Christina A. Risatti, Saravanababu Murugesan, 2014, The Journal of organic chemistry.

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 4. Synthesis of the 6-Azaindole Core

Richard L. Schild, Martin D. Eastgate, Christina A. Risatti, 2017 .

C-H Arylation in the Formation of a Complex Pyrrolopyridine, the Commercial Synthesis of the Potent JAK2 Inhibitor, BMS-911543.

Martin D. Eastgate, Paul C. Lobben, R. J. Fox, 2018, The Journal of organic chemistry.

Effects of Multiple Catalyst Deactivation Pathways and Continuous Ligand Recycling on the Kinetics of Pd-Catalyzed C-N Coupling Reactions.

Martin D. Eastgate, Maxime C Soumeillant, Y. Hsiao, 2018, The Journal of organic chemistry.

Development of a Commercial Process for Deucravacitinib, a Deuterated API for TYK2 Inhibition

Jianji Wang, Bahar Inankur, E. Simmons, 2022, Organic Process Research & Development.

Mild and general methods for the palladium-catalyzed cyanation of aryl and heteroaryl chlorides.

R. Cherney, Maxime C Soumeillant, C. Tarby, 2007, Organic letters.

Synthesis of HIV-Maturation Inhibitor BMS-955176 from Betulin by an Enabling Oxidation Strategy.

Qi Gao, Matthew W. Haley, Zhongmin Xu, 2017, The Journal of organic chemistry.

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 2. Strategic Selections in the Transition from an Enabling Route to a Commercial Synthesis

Bin Zheng, Ke Chen, Martin D. Eastgate, 2017 .

Rhodium-Catalyzed Cyclopropanation of Alkenes with Dimethyl Diazomalonate

M. Fenster, Maxime C Soumeillant, F. González-Bobes, 2008 .

Synthesis of chiral α-substituted N-[((2S)-2-hydroxy-2-phenyl)-ethyl]-2-phenylglycine derivatives by diastereocontrolled alkylation of (6 R)-2,3,5,6-tetrahydro-3,6-diaryl-N-[(2′R)-(2′-methyl)phenyl-methyl]-4H-1,4-oxazin-2-ones

Maxime C Soumeillant, D. Bouzard, P. Remuzon, 1997 .

Adventures in Atropisomerism: Development of a Robust, Diastereoselective, Lithium-Catalyzed Atropisomer-Forming Active Pharmaceutical Ingredient Step

Thomas M. Razler, Antonio Ramirez, S. Wisniewski, 2018, Organic Process Research & Development.

Use of a Field-Portable XRF Instrument To Facilitate Metal Catalyst Scavenger Screening

N. Lewen, Jun Qiu, Maxime C Soumeillant, 2015 .

Kilogram Synthesis of a Selective Serotonin Reuptake Inhibitor

R. Livingston, Chien-Kuang Chen, S. Gingras, 2008 .

A Practical Synthesis of l-Valyl-pyrrolidine-(2R)-boronic Acid: Efficient Recycling of the Costly Chiral Auxiliary (+)-Pinanediol

Maxime C Soumeillant, P. Manchand, D. Kronenthal, 2002 .

Chemical and Enzymatic Resolution of (R,S)-N-(tert-Butoxycarbonyl)-3-hydroxymethylpiperidine

Ramesh N. Patel, A. Goswami, K. D. Mirfakhrae, 2001 .

4-Hydroxy-2-methyl-3(2H)-isothiazolone-1,1-dioxide as protecting group of 4-(N-methylaminosulfonyl)methylphenylhydrazine during Fischer indole synthesis

Maxime C Soumeillant, J. Jacquet, D. Bouzard, 1995 .