| 11-step total synthesis of teleocidins B-1–B-4 H Nakamura, K Yasui, Y Kanda, PS Baran Journal of the American Chemical Society 141 (4), 1494-1497, 2019 | 72 | 2019 |
| Nickel-catalyzed decarboxylation of aryl carbamates for converting phenols into aromatic amines A Nishizawa, T Takahira, K Yasui, H Fujimoto, T Iwai, M Sawamura, ... Journal of the American Chemical Society 141 (18), 7261-7265, 2019 | 58 | 2019 |
| C− O Activation by a Rhodium Bis (N‐Heterocyclic Carbene) Catalyst: Aryl Carbamates as Arylating Reagents in Directed C− H Arylation M Tobisu, K Yasui, Y Aihara, N Chatani Angewandte Chemie 129 (7), 1903-1906, 2017 | 45 | 2017 |
| Rhodium-catalyzed cross-coupling of aryl carbamates with arylboron reagents K Nakamura, K Yasui, M Tobisu, N Chatani Tetrahedron 71 (26-27), 4484-4489, 2015 | 39 | 2015 |
| N‐Heterocyclic Carbene Catalyzed Concerted Nucleophilic Aromatic Substitution of Aryl Fluorides Bearing α, β‐Unsaturated Amides K Yasui, M Kamitani, M Tobisu Angewandte Chemie International Edition 58 (40), 14157-14161, 2019 | 37 | 2019 |
| Single–carbon atom transfer to α, β-unsaturated amides from N-heterocyclic carbenes M Kamitani, B Nakayasu, H Fujimoto, K Yasui, T Kodama, M Tobisu Science 379 (6631), 484-488, 2023 | 35 | 2023 |
| N-Heterocyclic Carbene-Catalyzed Truce–Smiles Rearrangement of N-Arylacrylamides via the Cleavage of Unactivated C(aryl)–N Bonds K Yasui, M Kamitani, H Fujimoto, M Tobisu Organic Letters 23 (5), 1572-1576, 2021 | 29 | 2021 |
| Rhodium-catalyzed C–O bond alkynylation of aryl carbamates with propargyl alcohols K Yasui, N Chatani, M Tobisu Organic letters 20 (7), 2108-2111, 2018 | 27 | 2018 |
| Rhodium-catalyzed reductive cleavage of aryl carbamates using isopropanol as a reductant K Yasui, M Higashino, N Chatani, M Tobisu Synlett 28 (19), 2569-2572, 2017 | 20 | 2017 |
| Chromium-catalyzed, regioselective cross-coupling of C–O bonds by using organic bromides as reactants J Tang, M Luo, X Zeng Synlett 28 (19), 2577-2580, 2017 | 19 | 2017 |
| Construction of Tricyclic Nitrogen Heterocycles by a Gold (I)‐Catalyzed Cascade Cyclization of Allenynes and Application to Polycyclic π‐Electron Systems H Komatsu, T Ikeuchi, H Tsuno, N Arichi, K Yasui, S Oishi, S Inuki, ... Angewandte Chemie 133 (52), 27225-27231, 2021 | 14 | 2021 |
| The Effect of the Leaving Group in N-Heterocyclic Carbene-Catalyzed Nucleophilic Aromatic Substitution Reactions K Yasui, M Kamitani, H Fujimoto, M Tobisu Bulletin of the Chemical Society of Japan 93 (12), 1424-1429, 2020 | 11 | 2020 |
| Leaving Group Ability in Nucleophilic Aromatic Amination by Sodium Hydride–Lithium Iodide Composite JH Pang, DY Ong, K Watanabe, R Takita, S Chiba Synthesis 52 (03), 393-398, 2020 | 8 | 2020 |
| Non-Classical Molecular Activation by Phosphines and N-Heterocyclic Carbenes and Its Application to Catalytic Reactions H Fujimoto, K Yasui, M Tobisu Bulletin of the Chemical Society of Japan 96 (9), 872-886, 2023 | 6 | 2023 |
| The Synthesis and Biological Evaluation of Indolactam Alkaloids M Mendoza, R Eom, C Salas, J Haynes-Smith, KL Billingsley Synthesis 51 (23), 4443-4451, 2019 | 6 | 2019 |
| Pd-catalysed C–H alkynylation of benzophospholes Y Tokura, S Xu, K Yasui, Y Nishii, K Hirano Chemical Communications 60 (20), 2792-2795, 2024 | 5 | 2024 |
| Nickel-Catalyzed Electrophilic Amination of the Biphenylene C–C σ-Bond T Inoue, S Nishino, K Yasui, K Hirano Organic Letters, 2024 | 2 | 2024 |
| Late-stage modification of π-electron systems based on asymmetric oxidation of a medium-sized sulfur-containing ring M Hayakawa, S Horike, Y Hijikata, K Yasui, S Yamaguchi, A Fukazawa Chemical Communications 58 (15), 2548-2551, 2022 | 2 | 2022 |
| Late-Stage Derivatization of Buflavine by Nickel-Catalyzed Direct Substitution of a Methoxy Group via C–O Bond Activation R Shimazumi, K Morita, T Yoshida, K Yasui, M Tobisu Synthesis 53 (17), 3037-3044, 2021 | 2 | 2021 |
| Cluster Preface: C–O And Related Bond Activation M Tobisu, N Chatani, V Snieckus Synlett 28 (19), 2559-2560, 2017 | 2 | 2017 |
Phil BaranProfessor of Chemistry, The Scripps Research Institute在 scripps.edu 的电子邮件经过验证
