Gregory Louis Beutner
Affiliations: | 1998-2004 | University of Illinois, Urbana-Champaign, Urbana-Champaign, IL |
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"Gregory Beutner"Mean distance: 8.4 | S | N | B | C | P |
Parents
Sign in to add mentorScott 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 |