| Iron-Catalyzed C–H Bond Activation R Shang, L Ilies, E Nakamura Chemical Reviews 117 (13), 9086–9139, 2017 | 900 | 2017 |
| Photocatalytic decarboxylative alkylations mediated by triphenylphosphine and sodium iodide MC Fu, R Shang, B Zhao, B Wang, Y Fu Science 363 (6434), 1429-1434, 2019 | 648 | 2019 |
| Transition metal-catalyzed decarboxylative cross-coupling reactions R Shang, L Liu Science China Chemistry 54, 1670-1687, 2011 | 456 | 2011 |
| A cyclic phosphate-based battery electrolyte for high voltage and safe operation Q Zheng, Y Yamada, R Shang, S Ko, YY Lee, K Kim, E Nakamura, ... Nature Energy 5, 291–298, 2020 | 351 | 2020 |
| Copper‐catalyzed decarboxylative cross‐coupling of potassium polyfluorobenzoates with aryl iodides and bromides R Shang, Y Fu, Y Wang, Q Xu, HZ Yu, L Liu Angewandte Chemie International Edition 48 (49), 9350-9354, 2009 | 345 | 2009 |
| Transition-Metal-Catalyzed Organic Reactions under Visible Light: Recent Developments and Future Perspectives WM Cheng, R Shang ACS Catalysis 10, 9170–9196, 2020 | 307 | 2020 |
| Synthesis of aromatic esters via Pd-catalyzed decarboxylative coupling of potassium oxalate monoesters with aryl bromides and chlorides R Shang, Y Fu, JB Li, SL Zhang, QX Guo, L Liu Journal of the American Chemical Society 131 (16), 5738-5739, 2009 | 302 | 2009 |
| Irradiation-Induced Heck Reaction of Unactivated Alkyl Halides at Room Temperature GZ Wang, R Shang, WM Cheng, Y Fu Journal of the American Chemical Society 139 (50), 18307–18312, 2017 | 294 | 2017 |
| β-Arylation of Carboxamides Via Iron-Catalyzed C(sp3)–H Bond Activation R Shang, R Shang New Carbon–Carbon Coupling Reactions Based on Decarboxylation and Iron …, 2017 | 286 | 2017 |
| Palladium-catalyzed decarboxylative couplings of 2-(2-azaaryl) acetates with aryl halides and triflates R Shang, ZW Yang, Y Wang, SL Zhang, L Liu Journal of the American Chemical Society 132 (41), 14391-14393, 2010 | 280 | 2010 |
| Photoredox/Brønsted Acid Co-Catalysis Enabling Decarboxylative Coupling of Amino Acid and Peptide Redox-Active Esters with N-Heteroarenes WM Cheng, R Shang, Y Fu ACS Catalysis 7 (1), 907–911, 2017 | 268 | 2017 |
| Iron-Catalyzed Directed C (sp2)-H and C (sp3)-H Functionalization with Trimethylaluminum R Shang, L Ilies, E Nakamura Journal of the American Chemical Society 137, 7660-7663, 2015 | 256 | 2015 |
| Synthesis of α‐Aryl Nitriles through Palladium‐Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates R Shang, DS Ji, L Chu, Y Fu, L Liu Angewandte Chemie International Edition 50 (19), 4470-4474, 2011 | 254 | 2011 |
| Theoretical analysis of factors controlling Pd-catalyzed decarboxylative coupling of carboxylic acids with olefins SL Zhang, Y Fu, R Shang, QX Guo, L Liu Journal of the American Chemical Society 132 (2), 638-646, 2010 | 247 | 2010 |
| Photoredox‐Catalysed Decarboxylative Alkylation of N‐Heteroarenes with N‐(Acyloxy) phthalimides WM Cheng, R Shang, MC Fu, Y Fu Chemistry-A European Journal 23 (11), 2537-2541, 2017 | 210 | 2017 |
| Pd-catalyzed decarboxylative cross coupling of potassium polyfluorobenzoates with aryl bromides, chlorides, and triflates R Shang, Q Xu, YY Jiang, Y Wang, L Liu Organic Letters 12 (5), 1000-1003, 2010 | 201 | 2010 |
| Irradiation-Induced Palladium-Catalyzed Decarboxylative Heck Reaction of Aliphatic N-(Acyloxy) phthalimides at Room Temperature GZ Wang, R Shang, Y Fu Organic letters 20 (3), 888–891, 2018 | 190 | 2018 |
| Decarboxylative 1, 4-addition of α-oxocarboxylic acids with Michael acceptors enabled by photoredox catalysis GZ Wang, R Shang, WM Cheng, Y Fu Organic letters 17 (19), 4830-4833, 2015 | 180 | 2015 |
| Boron‐catalyzed N‐alkylation of amines using carboxylic acids MC Fu, R Shang, WM Cheng, Y Fu Angewandte Chemie International Edition 54 (31), 9042-9046, 2015 | 180 | 2015 |
| Iron-catalyzed C (sp2)–H Bond Functionalization with Organoboron Compounds R Shang, L Ilies, S Asako, E Nakamura Journal of the American Chemical Society 136 (41), 14349–14352, 2014 | 167 | 2014 |
Eiichi NakamuraUniversity Professor, Department of Chemistry, The University of Tokyo確認したメール アドレス: chem.s.u-tokyo.ac.jp
