Nitinchandra D Patel

发表

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 .

Sequential C-H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor.

Jinhua J. Song, Bing-Shiou Yang, Jun Wang, 2016, Journal of the American Chemical Society.

Reengineered BI-DIME Ligand Core Based on Computer Modeling to Increase Selectivity in Asymmetric Suzuki–Miyaura Coupling for the Challenging Axially Chiral HIV Integrase Inhibitor

Jinhua J. Song, C. Senanayake, N. Yee, 2016 .

A general and special catalyst for Suzuki-Miyaura coupling processes.

C. Senanayake, A. White, Xudong Wei, 2010, Angewandte Chemie.

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.

A highly convergent and efficient synthesis of a macrocyclic hepatitis C virus protease inhibitor BI 201302.

C. Senanayake, Xudong Wei, N. Yee, 2013, Organic letters.

A Computational Investigation of the Ligand-Controlled Cu-Catalyzed Site-Selective Propargylation and Allenylation of Carbonyl Compounds

C. Senanayake, M. Kozlowski, K. Fandrick, 2017, Organic letters.

Development of an asymmetric synthesis of a chiral quaternary FLAP inhibitor.

Jinhua J. Song, C. Senanayake, P. Mahaney, 2015, The Journal of organic chemistry.

Early Development Scale-Up of a Structurally-Challenging 5-Lipoxygenase Activating Protein (FLAP) Inhibitor

Jinhua J. Song, Jun Wang, C. Senanayake, 2017 .

Efficient chiral monophosphorus ligands for asymmetric Suzuki-Miyaura coupling reactions.

M. Hao, C. Senanayake, Xudong Wei, 2012, Organic letters.

Development of an Efficient Asymmetric Synthesis of the Chiral Quaternary 5-Lipoxygenase Activating Protein Inhibitor

Jinhua J. Song, C. Senanayake, J. Mulder, 2016 .

The P-Chiral Phosphane Ligand (MeO-BIBOP) for Efficient and Practical Large-Scale Rh-Catalyzed Asymmetric Hydrogenation of N-Acetyl Enamides with High TONs

Jun Wang, C. Senanayake, N. Yee, 2013 .

One‐Pot Synthesis of 2,5‐Disubstituted Pyrimidines from Nitriles.

C. Senanayake, J. Mulder, Xudong Wei, 2013 .

One-pot synthesis of 2,5-disubstituted pyrimidines from nitriles.

C. Senanayake, J. Mulder, Xudong Wei, 2013, The Journal of organic chemistry.

Efficient monophosphorus ligands for palladium-catalyzed Miyaura borylation.

C. Senanayake, Xudong Wei, N. Yee, 2011, Organic letters.

Novel and efficient chiral bisphosphorus ligands for rhodium-catalyzed asymmetric hydrogenation.

C. Senanayake, A. White, Xudong Wei, 2010, Organic letters.

Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki-Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis.

Jinhua J. Song, C. Senanayake, M. Kozlowski, 2018, ACS catalysis.

A General and Practical Synthesis of N-Aryl-3-[4-(imidazol-4-yl)-1,2,3-triazol-1-yl]benzamide Anti-Inflammatory Cytokine Inhibitors

C. Senanayake, S. Rodrı́guez, R. Frutos, 2014 .

Copper-catalyst-controlled site-selective allenylation of ketones and aldehydes with propargyl boronates.

C. Senanayake, K. Fandrick, Daniel R Fandrick, 2013, Organic letters.

Ligand-Accelerated Stereoretentive Suzuki-Miyaura Coupling of Unprotected 3,3'-Dibromo-BINOL.

C. Senanayake, N. Yee, Shengli Ma, 2016, The Journal of organic chemistry.

Efficient asymmetric synthesis of structurally diverse P-stereogenic phosphinamides for catalyst design.

Jinhua J. Song, C. Senanayake, N. Yee, 2015, Angewandte Chemie.

A Practical Asymmetric Synthesis of Isopropyl (1R,2S)-Dehydrocoronamate

C. Senanayake, Xudong Wei, N. Yee, 2011 .

Concise and Practical Asymmetric Synthesis of a Challenging Atropisomeric HIV Integrase Inhibitor.

Y. Tsantrizos, Jiang-Ping Wu, C. Senanayake, 2015, Angewandte Chemie.

Addressing the configuration stability of lithiated secondary benzylic carbamates for the development of a noncryogenic stereospecific boronate rearrangement.

Jinhua J. Song, C. Senanayake, J. Mulder, 2014, Organic letters.

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

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

Start selective and rigidify: The discovery path towards a next generation of EGFR tyrosine kinase inhibitors.

Julian E. Fuchs, P. Ettmayer, A. Baum, 2019, Journal of medicinal chemistry.

Development of an Efficient Synthesis of (2-Aminopyrimidin-5-yl) Boronic Acid

Jinhua J. Song, C. Senanayake, J. Mulder, 2016 .

Effective BI‐DIME Ligand for Suzuki–Miyaura Cross‐Coupling Reactions in Water with 500 ppm Palladium Loading and Triton X

C. Senanayake, N. Yee, K. Fandrick, 2017 .

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 .