Gregory Louis Beutner

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1998-2004 University of Illinois, Urbana-Champaign, Urbana-Champaign, IL 
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"Gregory Beutner"
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Scott E. Denmark grad student 1998-2004 UIUC
 (Lewis base activation of Lewis acids in asymmetric aldol reactions of silyl ketene acetals.)
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Publications

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Gallagher WP, Beutner GL, Wadzinski TJ, et al. (2020) Selective opening of nucleoside derived acetals to form highly functionalized vinyl ethers Tetrahedron Letters. 61: 151750
Xiang J, Shang M, Kawamata Y, et al. (2019) Hindered dialkyl ether synthesis with electrogenerated carbocations. Nature
Fraunhoffer KJ, DelMonte AJ, Beutner GL, et al. (2019) Rapid Development of a Commercial Process for Linrodostat, an Indoleamine 2,3-Dioxygenase (IDO) Inhibitor Organic Process Research & Development. 23: 2482-2498
Beutner GL, Bultman MS, Cohen BM, et al. (2019) Follow the Silyl Cation: Insights into the Vorbrüggen Reaction Organic Process Research & Development. 23: 2050-2056
Beutner GL, Coombs JR, Green RA, et al. (2019) Palladium-Catalyzed Amidation and Amination of (Hetero)aryl Chlorides under Homogeneous Conditions Enabled by a Soluble DBU/NaTFA Dual-Base System Organic Process Research & Development. 23: 1529-1537
Beutner GL, Cohen BM, DelMonte AJ, et al. (2019) Revisiting the Cleavage of Evans Oxazolidinones with LiOH/H2O2 Organic Process Research & Development. 23: 1378-1385
Stevens JM, Parra-Rivera AC, Dixon DD, et al. (2018) Direct Lewis Acid-Catalyzed Conversion of Enantioenriched N-Acyl Oxazolidinones to Chiral Esters, Amides, and Acids. The Journal of Organic Chemistry
Fox RJ, Cuniere NL, Bakrania L, et al. (2018) C-H Arylation in the Formation of a Complex Pyrrolopyridine, the Commercial Synthesis of the Potent JAK2 Inhibitor, BMS-911543. The Journal of Organic Chemistry
Beutner GL, Young IS, Davies ML, et al. (2018) TCFH-NMI: Direct Access to N-Acyl Imidazoliums for Challenging Amide Bond Formations. Organic Letters
Beutner G, Carrasquillo R, Geng P, et al. (2018) Adventures in Atropisomerism: Total Synthesis of a Complex Active Pharmaceutical Ingredient with Two Chirality Axes. Organic Letters
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