D. S. Treitler

发表

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

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

Simple reagents for direct halonium-induced polyene cyclizations.

S. Snyder, D. Treitler, D. S. Treitler, 2010, Journal of the American Chemical Society.

A two-step mimic for direct, asymmetric bromonium- and chloronium-induced polyene cyclizations

S. Snyder, D. Treitler, D. S. Treitler, 2010 .

Process Development and Scale-up of a Multicomponent Synthesis of a 3-Methyl-1-aryl-1,2,4-triazole Building Block

Kristine M. Smith, Thomas E. La Cruz, S. Leung, 2020 .

Polymerization of enantiopure monomers using syndiospecific catalysts: a new approach to sequence control in polymer synthesis.

G. Coates, T. Roisnel, Pascal M. Castro, 2009, Journal of the American Chemical Society.

Et2SBrSbCl5Br: an effective reagent for direct bromonium-induced polyene cyclizations.

Scott A Snyder, S. Snyder, D. Treitler, 2009, Angewandte Chemie.

Synthesis of Et2SBr• SbCI5Br and Its Use in Biomimetic Brominative Polyene Cyclizations

S. Snyder, D. S. Treitler, 2012 .

Green Chemistry Articles of Interest to the Pharmaceutical Industry

Rachel Munday, A. Steven, P. Richardson, 2018, Organic Process Research & Development.

Development and Demonstration of a Safer Protocol for the Synthesis of 5-Aryltetrazoles from Aryl Nitriles

S. Leung, Mark D. Lindrud, D. S. Treitler, 2017 .

Low Pressure Carbonylation of Epoxides to β‐Lactones

G. Coates, J. W. Kramer, D. Treitler, 2009 .

Concise synthetic approaches for the Laurencia family: formal total syntheses of (±)-laurefucin and (±)-E- and (±)-Z-pinnatifidenyne.

S. Snyder, I. Moga, D. S. Treitler, 2012, Journal of the American Chemical Society.

A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia-type bromoethers.

S. Snyder, W. Sattler, D. Treitler, 2011, Journal of the American Chemical Society.

Reagents and Strategies for the Total Synthesis of Halogenated Natural Products

D. S. Treitler, 2012 .

P(III) vs P(V): A P(V) Reagent for Thiophosphoramidate Linkages and Application to an Asymmetric Synthesis of a Cyclic Dinucleotide STING Agonist.

Martin D. Eastgate, C. Hang, Hua-Chia Tai, 2021, The Journal of organic chemistry.

Evaluation of HIV-1 inhibition by stereoisomers and analogues of the sesquiterpenoid hydroquinone peyssonol A.

N. Meanwell, M. Krystal, S. Snyder, 2013, Bioorganic & medicinal chemistry letters.

Halonium‐Induced Cyclization Reactions

S. Snyder, D. S. Treitler, A. P. Brucks, 2012 .

How Dangerous Is Too Dangerous? A Perspective on Azide Chemistry.

S. Leung, D. S. Treitler, 2022, Journal of Organic Chemistry.

Mutagenic Impurities in 1-Hydroxybenzotriazole (HOBt)

James Chadwick, D. Treitler, Andrew S. Marriott, 2019, Organic Process Research & Development.

Explorations into the Potential of Chiral Sulfonium Reagents to Effect Asymmetric Halonium Additions to Isolated Alkenes

S. Snyder, Shu-An Liu, D. S. Treitler, 2013, Synthesis.

Zinc Acetate-Promoted Buchwald-Hartwig Couplings of Heteroaromatic Amines.

Martin D. Eastgate, J. Janey, E. Simmons, 2017, The Journal of organic chemistry.