| Decarboxylative C(sp3)–N cross-coupling via synergetic photoredox and copper catalysis R Mao, A Frey, J Balon, X Hu Nature Catalysis 1 (2), 120-126, 2018 | 232 | 2018 |
| Enantioselective C (sp 3)–C (sp 3) cross-coupling of non-activated alkyl electrophiles via nickel hydride catalysis S Bera#, R Mao#, X Hu Nature Chemistry 13, 270-277, 2021 | 168 | 2021 |
| Decarboxylative C(sp3)−O Cross‐Coupling R Mao, J Balon, X Hu Angewandte Chemie International Edition 57 (41), 13624-13628, 2018 | 121 | 2018 |
| Cross‐Coupling of Alkyl Redox‐Active Esters with Benzophenone Imines: Tandem Photoredox and Copper Catalysis R Mao, J Balon, X Hu Angewandte Chemie 130 (30), 9645-9648, 2018 | 113 | 2018 |
| Photoinduced C–S Bond Cleavage of Thioglycosides and Glycosylation RZ Mao, F Guo, DC Xiong, Q Li, J Duan, XS Ye Organic letters 17 (22), 5606-5609, 2015 | 79 | 2015 |
| Pd(II)-Catalyzed Ortho Arylation of 6-Arylpurines with Aryl Iodides via Purine-Directed C−H Activation: A New Strategy for Modification of 6-Arylpurine Derivatives HM Guo, LL Jiang, HY Niu, WH Rao, L Liang, RZ Mao, DY Li, GR Qu Organic Letters 13 (8), 2008-2011, 2011 | 71 | 2011 |
| Copper-Catalyzed Intermolecular Functionalization of Unactivated C(sp3)–H Bonds and Aliphatic Carboxylic Acids R Mao, S Bera, AC Turla, X Hu Journal of the American Chemical Society 143 (36), 14667-14675, 2021 | 60 | 2021 |
| CuBr Catalyzed C–N cross coupling reaction of purines and diaryliodonium salts to 9-arylpurines HY Niu, C Xia, GR Qu, Q Zhang, Y Jiang, RZ Mao, DY Li, HM Guo Organic & Biomolecular Chemistry 9 (14), 5039-5042, 2011 | 56 | 2011 |
| Light-driven highly efficient glycosylation reactions RZ Mao, DC Xiong, F Guo, Q Li, J Duan, XS Ye Organic Chemistry Frontiers 3 (6), 737-743, 2016 | 55 | 2016 |
| Tandem Photoredox and Copper-Catalyzed Decarboxylative C(sp3)–N Coupling of Anilines and Imines Using an Organic Photocatalyst G Barzanò, R Mao, M Garreau, J Waser, X Hu Organic letters 22 (14), 5412-5416, 2020 | 43 | 2020 |
| Visible Light Photoredox-Catalyzed O-Sialylation Using Thiosialoside Donors Y Yu, DC Xiong, RZ Mao, XS Ye The Journal of Organic Chemistry 81 (16), 7134-7138, 2016 | 40 | 2016 |
| Deoxygenative trifluoromethylthiolation of carboxylic acids R Mao, S Bera, A Cheseaux, X Hu Chemical science 10 (41), 9555-9559, 2019 | 38 | 2019 |
| Pd (II)-catalyzed one-pot, three-step route for the synthesis of unsymmetrical acridines HM Guo*, RZ Mao, QT Wang, HY Niu, MS Xie, GR Qu* Organic letters 15 (21), 5460-5463, 2013 | 33 | 2013 |
| Photocatalytic Decarboxylative Coupling of Aliphatic N‐hydroxyphthalimide Esters with Polyfluoroaryl Nucleophiles X Yi, R Mao, L Lavrencic, X Hu Angewandte Chemie International Edition 60 (44), 23557-23563, 2021 | 25 | 2021 |
| Chemodivergent C(sp3)–H and C(sp2)–H cyanomethylation using engineered carbene transferases J Zhang, AO Maggiolo, E Alfonzo, R Mao, NJ Porter, NM Abney, ... Nature catalysis 6 (2), 152-160, 2023 | 15 | 2023 |
| Enantio- and Diastereoenriched Enzymatic Synthesis of 1,2,3-Polysubstituted Cyclopropanes from (Z/E)-Trisubstituted Enol Acetates R Mao, DJ Wackelin, CS Jamieson, T Rogge, S Gao, A Das, DM Taylor, ... Journal of the American Chemical Society 145 (29), 16176–16185, 2023 | 14 | 2023 |
| Lithium Chloride Catalyzed Aza-Michael Addition of Pyrazoles to α, β-Unsaturated Imides H Zhou, X Xiang, B Ma, G Wang, Z Zhang, J Yang Synthesis 51 (16), 3142-3150, 2019 | 12 | 2019 |
| Enzymatic Assembly of Diverse Lactone Structures: An Intramolecular C–H Functionalization Strategy DJ Wackelin#, R Mao#, KM Sicinski, Y Zhao, A Das, K Chen, FH Arnold Journal of the American Chemical Society, 2024 | 10 | 2024 |
| Visible-light-promoted 3, 5-dimethoxyphenyl glycoside activation and glycosylation Y Cao, M Zhou, RZ Mao, Y Zou, F Xia, DK Liu, J Liu, Q Li, DC Xiong, ... Chemical Communications 57 (83), 10899-10902, 2021 | 10 | 2021 |
| N-9 Alkylation of purines via light-promoted and metal-free radical relay R Mao, L Sun, YS Wang, MM Zhou, DC Xiong, Q Li, XS Ye Chinese Chemical Letters 29 (1), 61-64, 2018 | 10 | 2018 |
Xile HuEcole Polytechnique Fédérale de Lausanne確認したメール アドレス: epfl.ch