| Lewis base catalysis in organic synthesis SE Denmark, GL Beutner Angewandte Chemie International Edition 47 (9), 1560-1638, 2008 | 1410 | 2008 |
| Catalytic, enantioselective, vinylogous aldol reactions SE Denmark, JR Heemstra Jr, GL Beutner Angewandte Chemie International Edition 44 (30), 4682-4698, 2005 | 509 | 2005 |
| Hindered dialkyl ether synthesis with electrogenerated carbocations J Xiang, M Shang, Y Kawamata, H Lundberg, SH Reisberg, M Chen, ... Nature 573 (7774), 398-402, 2019 | 313 | 2019 |
| Lewis base activation of Lewis acids: catalytic, enantioselective addition of silyl ketene acetals to aldehydes SE Denmark, GL Beutner, T Wynn, MD Eastgate Journal of the American Chemical Society 127 (11), 3774-3789, 2005 | 284 | 2005 |
| Lewis base activation of Lewis acids. Addition of silyl ketene acetals to aldehydes SE Denmark, T Wynn, GL Beutner Journal of the American Chemical Society 124 (45), 13405-13407, 2002 | 213 | 2002 |
| Lewis base activation of Lewis acids. Vinylogous aldol reactions SE Denmark, GL Beutner Journal of the American Chemical Society 125 (26), 7800-7801, 2003 | 193 | 2003 |
| Low molecular weight cationic lipids for oligonucleotide delivery MG Stanton, BW Budzik, GL Beutner, H Liao | 169 | 2021 |
| TCFH–NMI: Direct Access to N-Acyl Imidazoliums for Challenging Amide Bond Formations GL Beutner, IS Young, ML Davies, MR Hickey, H Park, JM Stevens, Q Ye Organic letters 20 (14), 4218-4222, 2018 | 142 | 2018 |
| Lewis base catalysis of the Mukaiyama directed aldol reaction: 40 years of inspiration and advances GL Beutner, SE Denmark Angewandte Chemie International Edition 52 (35), 9086-9096, 2013 | 128 | 2013 |
| Low molecular weight cationic lipids for oligonucleotide delivery MG Stanton, BW Budzik, GL Beutner, H Liao US Patent 9,669,097, 2017 | 102 | 2017 |
| Rhenium-catalyzed 1, 3-isomerization of allylic alcohols: Scope and chirality transfer C Morrill, GL Beutner, RH Grubbs The Journal of Organic Chemistry 71 (20), 7813-7825, 2006 | 97 | 2006 |
| A highly efficient asymmetric synthesis of vernakalant J Limanto, ER Ashley, J Yin, GL Beutner, BT Grau, AM Kassim, MM Kim, ... Organic letters 16 (10), 2716-2719, 2014 | 94 | 2014 |
| Enantioselective ring opening of epoxides with silicon tetrachloride in the presence of a chiral Lewis base: mechanism studies SE Denmark, PA Barsanti, GL Beutner, TW Wilson Advanced Synthesis & Catalysis 349 (4‐5), 567-582, 2007 | 83 | 2007 |
| Palladium-catalyzed amidation and amination of (hetero) aryl chlorides under homogeneous conditions enabled by a soluble DBU/NaTFA dual-base system GL Beutner, JR Coombs, RA Green, B Inankur, D Lin, J Qiu, F Roberts, ... Organic Process Research & Development 23 (8), 1529-1537, 2019 | 59 | 2019 |
| Adventures in atropisomerism: total synthesis of a complex active pharmaceutical ingredient with two chirality axes G Beutner, R Carrasquillo, P Geng, Y Hsiao, EC Huang, J Janey, ... Organic letters 20 (13), 3736-3740, 2018 | 57 | 2018 |
| Expedient Synthesis of 3-Alkoxymethyl- and 3-Aminomethyl-Pyrazolo[3,4-b]pyridines GL Beutner, JT Kuethe, MM Kim, N Yasuda The Journal of Organic Chemistry 74 (2), 789-794, 2009 | 57 | 2009 |
| Scalable Synthesis of the Potent HIV Inhibitor BMS‐986001 by Non‐Enzymatic Dynamic Kinetic Asymmetric Transformation (DYKAT) A Ortiz, T Benkovics, GL Beutner, Z Shi, M Bultman, J Nye, C Sfouggatakis, ... Angewandte Chemie International Edition 54 (24), 7185-7188, 2015 | 54 | 2015 |
| Design, validation, and implementation of a rapid-injection NMR system SE Denmark, BJ Williams, BM Eklov, SM Pham, GL Beutner The Journal of Organic Chemistry 75 (16), 5558-5572, 2010 | 53 | 2010 |
| A Process Chemistry Benchmark for sp2–sp3 Cross Couplings GL Beutner, EM Simmons, S Ayers, CY Bemis, MJ Goldfogel, CL Joe, ... The Journal of Organic Chemistry 86 (15), 10380-10396, 2021 | 50 | 2021 |
| Development of a practical, asymmetric synthesis of the hepatitis C virus protease inhibitor MK-5172 J Kuethe, YL Zhong, N Yasuda, G Beutner, K Linn, M Kim, B Marcune, ... Organic letters 15 (16), 4174-4177, 2013 | 48 | 2013 |