Scott A. Savage

发表

Using In Silico Tools To Map the Structural Landscape of Nitroxyl (HNO Donor) Compounds

A. Sarjeant, J. Albrecht, Andrew J. Ilott, 2022, Crystal Growth & Design.

Preparation of Saxagliptin, a Novel DPP-IV Inhibitor

Gregory S Jones, R. Waltermire, Kolotuchin Sergei, 2009 .

Efficient Synthesis of 4-, 5-, and 6-Methyl-2,2‘-bipyridine by a Negishi Cross-Coupling Strategy Followed by High-Yield Conversion to Bromo- and Chloromethyl-2,2‘-bipyridines

C. Fraser, Adam P. Smith, Scott A. Savage, 1998 .

Development of Two Synthetic Approaches to an APJ Receptor Agonist Containing a Tetra-ortho-Substituted Biaryl Pyridone

Matthew J. Goldfogel, Matthew W. Haley, R. Vaidyanathan, 2021 .

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.

The Discovery and Chemical Development of BMS-919373: A Selective I Kur Inhibitor for the Potential Treatment of Atrial Fibrillation

Jason M. Stevens, Miao Yu, S. Wisniewski, 2020 .

Utilizing Native Directing Groups: Synthesis of a Selective IKur Inhibitor, BMS-919373, via a Regioselective C-H Arylation.

Jason M. Stevens, Miao Yu, S. Wisniewski, 2018, The Journal of organic chemistry.

Kinetic and mechanistic insight into the thermodynamic degradation of saxagliptin.

Antonio Ramirez, P. Benitez, Scott A. Savage, 2011, The Journal of organic chemistry.

Utilizing Native Directing Groups: Mechanistic Understanding of a Direct Arylation Leads to Formation of Tetracyclic Heterocycles via Tandem Intermolecular, Intramolecular C-H Activation.

Martin D. Eastgate, D. Blackmond, R. E. Plata, 2019, The Journal of organic chemistry.

Synthesis of Akt Inhibitor Ipatasertib. Part 2. Total Synthesis and First Kilogram Scale-up

M. W. Dong, J. Stults, D. Askin, 2014 .

A Practical Synthesis of a PI3K Inhibitor under Noncryogenic Conditions via Functionalization of a Lithium Triarylmagnesiate Intermediate

F. Gosselin, M. Reynolds, D. Askin, 2013 .

Manufacturing Development and Genotoxic Impurity Control Strategy of the Hedgehog Pathway Inhibitor Vismodegib

M. Reynolds, C. Venkatramani, R. Angelaud, 2016 .

The Medicinal Chemistry and Commercial Manufacturing Behind the Discovery and Development of the Hedgehog Inhibitor Vismodegib

D. Sutherlin, M. Reynolds, R. Angelaud, 2016 .

Revisiting a Classic Transformation: A Lossen Rearrangement Initiated by Nitriles and "Pseudo-Catalytic" in Isocyanate.

A. Ortiz, Sloan Ayers, N. Strotman, 2017, The Journal of organic chemistry.

Identification of C-2 hydroxyethyl imidazopyrrolopyridines as potent JAK1 inhibitors with favorable physicochemical properties and high selectivity over JAK2.

Jane R Kenny, Philippe Bergeron, Ignacio Aliagas, 2013, Journal of medicinal chemistry.

Discovery and optimization of C-2 methyl imidazopyrrolopyridines as potent and orally bioavailable JAK1 inhibitors with selectivity over JAK2.

Jane R Kenny, Philippe Bergeron, Tian Jin, 2012, Journal of medicinal chemistry.

A Practical and Robust Multistep Continuous Process for Manufacturing 5-Bromo-N-(tert-butyl)pyridine-3-sulfonamide

Antonio Ramirez, S. Leung, Miao Yu, 2019, Organic Process Research & Development.

Synthesis of 4‐, 5‐, and 6‐Methyl‐2,2′‐Bipyridine by a Negishi Cross‐Coupling Strategy: 5‐Methyl‐2,2′‐Bipyridine

J. Love, C. Fraser, Adam P. Smith, 2003 .

Synthesis of 4-, 5-, and 6-methyl-2,2'-bipyridine by a negishi cross-coupling strategy: 5-methyl-2,2'-bipyridine (2,2'-bipyridine, 5-methyl-)

J. Love, C. Fraser, L. Hegedus, 2002 .