| General principles and strategies for salting-out informed by the Hofmeister series AM Hyde, SL Zultanski, JH Waldman, YL Zhong, M Shevlin, F Peng Organic Process Research & Development 21 (9), 1355-1370, 2017 | 422 | 2017 |
| Pd-catalyzed N-arylation of secondary acyclic amides: catalyst development, scope, and computational study JD Hicks, AM Hyde, AM Cuezva, SL Buchwald Journal of the American Chemical Society 131 (46), 16720-16734, 2009 | 260 | 2009 |
| Orthogonal Pd-and Cu-based catalyst systems for C-and N-arylation of oxindoles RA Altman, AM Hyde, X Huang, SL Buchwald Journal of the American Chemical Society 130 (29), 9613-9620, 2008 | 187 | 2008 |
| Copper-promoted coupling of vinyl boronates and alcohols: a mild synthesis of allyl vinyl ethers RE Shade, AM Hyde, JC Olsen, CA Merlic Journal of the American Chemical Society 132 (4), 1202-1203, 2010 | 173 | 2010 |
| Lewis acid enhancement by hydrogen-bond donors for asymmetric catalysis SM Banik, A Levina, AM Hyde, EN Jacobsen Science 358 (6364), 761-764, 2017 | 160 | 2017 |
| A multifunctional catalyst that stereoselectively assembles prodrugs DA DiRocco, Y Ji, EC Sherer, A Klapars, M Reibarkh, J Dropinski, ... Science 356 (6336), 426-430, 2017 | 145 | 2017 |
| Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides X Shen, AM Hyde, SL Buchwald Journal of the American Chemical Society 132 (40), 14076-14078, 2010 | 139 | 2010 |
| Palladium‐Catalyzed γ‐Arylation of β, γ‐Unsaturated Ketones: Application to a One‐Pot Synthesis of Tricyclic Indolines AM Hyde, SL Buchwald Angewandte Chemie International Edition 47 (1), 177-180, 2008 | 107 | 2008 |
| Chiral thioureas promote enantioselective Pictet–Spengler cyclization by stabilizing every intermediate and transition state in the carboxylic acid-catalyzed reaction RS Klausen, CR Kennedy, AM Hyde, EN Jacobsen Journal of the American Chemical Society 139 (35), 12299-12309, 2017 | 94 | 2017 |
| Enantioselective Synthesis of Hemiaminals via Pd-Catalyzed C–N Coupling with Chiral Bisphosphine Mono-oxides H Li, KM Belyk, J Yin, Q Chen, A Hyde, Y Ji, S Oliver, MT Tudge, ... Journal of the American Chemical Society 137 (43), 13728-13731, 2015 | 94 | 2015 |
| Investigating the underappreciated hydrolytic instability of 1, 8-diazabicyclo [5.4. 0] undec-7-ene and related unsaturated nitrogenous bases AM Hyde, R Calabria, R Arvary, X Wang, A Klapars Organic Process Research & Development 23 (9), 1860-1871, 2019 | 65 | 2019 |
| Synthesis of 5, 5-disubstituted butenolides based on a Pd-catalyzed γ-arylation strategy AM Hyde, SL Buchwald Organic letters 11 (12), 2663-2666, 2009 | 63 | 2009 |
| Chiral sulfinamide/achiral sulfonic acid cocatalyzed enantioselective protonation of enol silanes EM Beck, AM Hyde, EN Jacobsen Organic letters 13 (16), 4260-4263, 2011 | 55 | 2011 |
| Model for the enantioselectivity of asymmetric intramolecular alkylations by bis-quaternized cinchona alkaloid-derived catalysts CQ He, A Simon, Y Lam, APJ Brunskill, N Yasuda, J Tan, AM Hyde, ... The Journal of Organic Chemistry 82 (16), 8645-8650, 2017 | 34 | 2017 |
| Synthesis of the GPR40 partial agonist MK-8666 through a kinetically controlled dynamic enzymatic ketone reduction AM Hyde, Z Liu, B Kosjek, L Tan, A Klapars, ER Ashley, YL Zhong, ... Organic letters 18 (22), 5888-5891, 2016 | 32 | 2016 |
| Application of the light-lever technique to the study of colloidal forces VSJ Craig, AM Hyde, RM Pashley Langmuir 12 (15), 3557-3562, 1996 | 29 | 1996 |
| A rational pre-catalyst design for bis-phosphine mono-oxide palladium catalyzed reactions Y Ji, H Li, AM Hyde, Q Chen, KM Belyk, KW Lexa, J Yin, EC Sherer, ... Chemical Science 8 (4), 2841-2851, 2017 | 26 | 2017 |
| Silanediol anion binding and enantioselective catalysis JW Attard, K Osawa, Y Guan, J Hatt, S Kondo, A Mattson Synthesis 51 (10), 2107-2115, 2019 | 20 | 2019 |
| Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods A Klapars, JYL Chung, J Limanto, R Calabria, LC Campeau, KR Campos, ... Chemical Science 12 (26), 9031-9036, 2021 | 16 | 2021 |
| A newly designed carbohydrate-derived alkylamine promotes Ullmann type C–N coupling catalyzed by copper in water G Zhou, W Chen, S Zhang, X Liu, Z Yang, X Ge, HJ Fan Synlett 30 (02), 193-198, 2019 | 15 | 2019 |
