| Difunctionalization of alkenes involving metal migration Y Li, D Wu, HG Cheng, G Yin Angewandte Chemie International Edition 59 (21), 7990-8003, 2020 | 282 | 2020 |
| Migratory arylboration of unactivated alkenes enabled by nickel catalysis W Wang, C Ding, Y Li, Z Li, Y Li, L Peng, G Yin Angewandte Chemie International Edition 58 (14), 4612-4616, 2019 | 116 | 2019 |
| Ligand-controlled nickel-catalyzed reductive relay cross-coupling of alkyl bromides and aryl bromides L Peng, Y Li, Y Li, W Wang, H Pang, G Yin ACS Catalysis 8 (1), 310-313, 2018 | 116 | 2018 |
| Reaction scope and mechanistic insights of nickel-catalyzed migratory Suzuki–Miyaura cross-coupling Y Li, Y Luo, L Peng, Y Li, B Zhao, W Wang, H Pang, Y Deng, R Bai, Y Lan, ... Nature Communications 11 (1), 417, 2020 | 106 | 2020 |
| Modular and facile access to chiral α-aryl phosphates via dual nickel-and photoredox-catalyzed reductive cross-coupling H Wang, P Zheng, X Wu, Y Li, T Xu Journal of the American Chemical Society 144 (9), 3989-3997, 2022 | 63 | 2022 |
| Modular access to substituted cyclohexanes with kinetic stereocontrol Y Li, Y Li, H Shi, H Wei, H Li, I Funes-Ardoiz, G Yin Science 376 (6594), 749-753, 2022 | 52 | 2022 |
| ChemLLM: A Chemical Large Language Model D Zhang, W Liu, Q Tan, J Chen, H Yan, Y Yan, J Li, W Huang, X Yue, ... arXiv preprint arXiv:2402.06852, 2024 | 49 | 2024 |
| Nickel/Brønsted acid dual-catalyzed regio-and enantioselective hydrophosphinylation of 1, 3-dienes: access to chiral allylic phosphine oxides J Long, Y Li, W Zhao, G Yin Chemical Science 13 (5), 1390-1397, 2022 | 46 | 2022 |
| Nickel/Brønsted acid-catalyzed chemo-and enantioselective intermolecular hydroamination of conjugated dienes J Long, P Wang, W Wang, Y Li, G Yin Iscience 22, 369-379, 2019 | 39 | 2019 |
| Practical Synthesis of Chiral Allylboronates by Asymmetric 1, 1‐Difunctionalization of Terminal Alkenes C Sun, Y Li, G Yin Angewandte Chemie 134 (37), e202209076, 2022 | 31 | 2022 |
| Accessing gpt-4 level mathematical olympiad solutions via monte carlo tree self-refine with llama-3 8b D Zhang, X Huang, D Zhou, Y Li, W Ouyang arXiv preprint arXiv:2406.07394, 2024 | 30 | 2024 |
| Nickel-catalyzed regio-and enantioselective borylative coupling of terminal alkenes with alkyl halides enabled by an anionic bisoxazoline ligand Z Li, H Shi, X Chen, L Peng, Y Li, G Yin Journal of the American Chemical Society 145 (25), 13603-13614, 2023 | 29 | 2023 |
| Synergistic Ni/Cu catalyzed migratory arylsilylation of terminal olefins B Zhao, Y Li, H Li, M Belal, L Zhu, G Yin Science Bulletin 66 (6), 570-577, 2021 | 26 | 2021 |
| Nickel-catalyzed migratory alkyl–alkyl cross-coupling reaction Y Li, Y Li, L Peng, D Wu, L Zhu, G Yin Chemical Science 11 (38), 10461-10464, 2020 | 26 | 2020 |
| Base‐Modulated 1, 3‐Regio‐and Stereoselective Carboboration of Cyclohexenes W Kong, Y Bao, L Lu, Z Han, Y Zhong, R Zhang, Y Li, G Yin Angewandte Chemie International Edition 62 (35), e202308041, 2023 | 17 | 2023 |
| Phosphine-Catalyzed Atroposelective Formal [3 + 2] Cycloaddition Desymmetrization of N-Arylmaleimides H Wang, Y Wei, Y Li, S Long, LJ Sun, S Li, YW Lin Organic Letters 24 (36), 6494-6498, 2022 | 17 | 2022 |
| Alkene 1, 1-difunctionalizations via organometallic-radical relay D Wu, W Kong, Y Bao, D Zhao, Y Li, G Yin Nature Catalysis 6 (11), 1030-1041, 2023 | 16 | 2023 |
| Molybdenum-Catalyzed Cross-Coupling of Benzyl Alcohols: Direct C–OH Bond Transformation via [2+ 2]-Type Addition and Elimination P Zhou, Y Li, T Xu Organic Letters 24 (23), 4218-4223, 2022 | 16 | 2022 |
| Photocatalytic vinyl radical-mediated multicomponent 1, 4-/1, 8-carboimination across alkynes and olefins/(hetero) arenes SS Li, YS Jiang, XL Luo, X Ran, Y Li, D Wu, CX Pan, PJ Xia Science China Chemistry 67 (2), 558-567, 2024 | 14 | 2024 |
| Enantioselective directed nickel-catalyzed three-component reductive arylalkylation of alkenes via the carbometalation/radical cross-coupling sequence Z Dong, C Xu, J Chang, S Zhou, P Sun, Y Li, LA Chen ACS Catalysis 14 (7), 4395-4406, 2024 | 13 | 2024 |
Guoyin Yin武汉大学E-mail megerősítve itt: whu.edu.cn