| Enantioselective formation of quaternary carbon stereocenters in natural product synthesis: a recent update C Li, SS Ragab, G Liu, W Tang Natural Product Reports 37 (2), 276-292, 2020 | 187 | 2020 |
| CuH-catalyzed enantioselective ketone allylation with 1, 3-dienes: scope, mechanism, and applications C Li, RY Liu, LT Jesikiewicz, Y Yang, P Liu, SL Buchwald Journal of the American Chemical Society 141 (12), 5062-5070, 2019 | 172 | 2019 |
| An efficient method for sterically demanding Suzuki–Miyaura coupling reactions Q Zhao, C Li, CH Senanayake, W Tang Chem. Eur. J 19 (7), 2261-2265, 2013 | 139 | 2013 |
| Efficient Synthesis of Sterically Hindered Arenes Bearing Acyclic Secondary Alkyl Groups by Suzuki–Miyaura Cross‐Couplings C Li, T Chen, B Li, G Xiao, W Tang Angewandte Chemie International Edition 54 (12), 3792-3796, 2015 | 92 | 2015 |
| Transition-metal-catalyzed alkyl Heck-type reactions D Kurandina, P Chuentragool, V Gevorgyan Synthesis 51 (05), 985-1005, 2019 | 89 | 2019 |
| Engaging Aldehydes in CuH‐Catalyzed Reductive Coupling Reactions: Stereoselective Allylation with Unactivated 1, 3‐Diene Pronucleophiles C Li, K Shin, RY Liu, SL Buchwald Angewandte Chemie 131 (47), 17230-17236, 2019 | 77 | 2019 |
| Transition-metal-free stereospecific cross-coupling with alkenylboronic acids as nucleophiles C Li, Y Zhang, Q Sun, T Gu, H Peng, W Tang Journal of the American Chemical Society 138 (34), 10774-10777, 2016 | 75 | 2016 |
| Addressing the challenges in suzuki–Miyaura cross-couplings by ligand design C Li, D Chen, W Tang Synlett 27 (15), 2183-2200, 2016 | 65 | 2016 |
| Stereoelectronic Effects in Ligand Design: Enantioselective Rhodium‐Catalyzed Hydrogenation of Aliphatic Cyclic Tetrasubstituted Enamides and Concise Synthesis of (R)‐Tofacitinib C Li, F Wan, Y Chen, H Peng, W Tang, S Yu, JC McWilliams, J Mustakis, ... Angewandte Chemie International Edition 58 (38), 13573-13583, 2019 | 60 | 2019 |
| Fully automated fast-flow synthesis of antisense phosphorodiamidate morpholino oligomers C Li, AJ Callahan, MD Simon, KA Totaro, AJ Mijalis, KS Phadke, G Zhang, ... Nature Communications 12 (1), 4396, 2021 | 47 | 2021 |
| Stereospecific nucleophilic substitution with arylboronic acids as nucleophiles in the presence of a CONH group D Tian, C Li, G Gu, H Peng, X Zhang, W Tang Angewandte Chemie International Edition 57 (24), 7176-7180, 2018 | 47 | 2018 |
| Sterically demanding aryl–alkyl Suzuki–Miyaura coupling C Li, G Xiao, Q Zhao, H Liu, T Wang, W Tang Organic Chemistry Frontiers 1 (3), 225-229, 2014 | 42 | 2014 |
| Automated flow synthesis of peptide–PNA conjugates C Li, AJ Callahan, KS Phadke, B Bellaire, CE Farquhar, G Zhang, ... ACS central science 8 (2), 205-213, 2021 | 28 | 2021 |
| Automated affinity selection for rapid discovery of peptide binders G Zhang, C Li, AJ Quartararo, A Loas, BL Pentelute Chemical Science 12 (32), 10817-10824, 2021 | 23 | 2021 |
| Rapid de novo discovery of peptidomimetic affinity reagents for human angiotensin converting enzyme 2 G Zhang, JS Brown, AJ Quartararo, C Li, X Tan, S Hanna, S Antilla, ... Communications Chemistry 5 (1), 8, 2022 | 22 | 2022 |
| Machine learning guides peptide nucleic acid flow synthesis and sequence design C Li, G Zhang, S Mohapatra, AJ Callahan, A Loas, R Gómez‐Bombarelli, ... Advanced Science 9 (34), 2201988, 2022 | 9 | 2022 |
| Recent developments of automated flow chemistry in pharmaceutical compounds synthesis J Wu, X Yang, Y Pan, T Zuo, Z Ning, C Li, Z Zhang Journal of Flow Chemistry 13 (4), 385-404, 2023 | 7 | 2023 |
| Automated Fast-Flow Synthesis of Peptide Nucleic Acid Conjugates C Li, AJ Callahan, KS Phadke, B Bellaire, CE Farquhar, G Zhang, ... | 3 | 2021 |
| Recent advances in metal-free peptide stapling strategies W Zhan, H Duan, C Li Chem & Bio Engineering 1 (7), 593-605, 2024 | 2 | 2024 |
| Automated Fast-Flow Synthesis of Antisense Phosphorodiamidate Morpholino Oligomers C Li, AJ Callahan, MD Simon, KA Totaro, AJ Mijalis, N Hartrampf, ... | 2 | 2020 |
