| Bidentate directing groups: an efficient tool in C–H bond functionalization chemistry for the expedient construction of C–C bonds S Rej, Y Ano, N Chatani Chemical Reviews 120 (3), 1788-1887, 2020 | 858 | 2020 |
| Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization Assisted by Removable Directing Groups S Rej, N Chatani Angewandte Chemie International Edition, 2018 | 373 | 2018 |
| Strategic evolution in transition metal-catalyzed directed C–H bond activation and future directions S Rej, A Das, N Chatani Coordination Chemistry Reviews 431, 213683, 2021 | 242 | 2021 |
| Overview of Regioselective and Stereoselective Catalytic Hydroboration of Alkynes S Rej, A Das, TK Panda Advanced Synthesis & Catalysis, 2021 | 103 | 2021 |
| Rhodium (I)-catalyzed C8-alkylation of 1-naphthylamide derivatives with alkenes through a bidentate picolinamide chelation system S Rej, N Chatani ACS Catalysis 8 (7), 6699-6706, 2018 | 65 | 2018 |
| Transient Imine as a Directing Group for the Metal-Free o-C–H Borylation of Benzaldehydes S Rej, N Chatani Journal of the American Chemical Society 143 (7), 2920-2929, 2021 | 58 | 2021 |
| Regio‐Selective Transition‐Metal‐Free C (sp2)‒H Borylation: A Subject of Practical and Ongoing Interest in Synthetic Organic Chemistry S Rej, N Chatani Angewandte Chemie International Edition, 2022 | 57 | 2022 |
| Multiply-bonded dinuclear complexes of early-transition metals as minimum entities of metal cluster catalysts S Rej, H Tsurugi, K Mashima Coordination Chemistry Reviews 355, 223-239, 2018 | 51 | 2018 |
| Group 1 and group 2 metal complexes supported by a bidentate bulky iminopyrrolyl ligand: synthesis, structural diversity, and ε-caprolactone polymerization study RK Kottalanka, A Harinath, S Rej, TK Panda Dalton Transactions 44 (46), 19865-19879, 2015 | 37 | 2015 |
| Aluminium Complexes: Next-Generation Catalysts in Selective Hydroboration A Das, S Rej, TK Panda Dalton Transactions, 2022 | 33 | 2022 |
| Dehalogenation of vicinal dihalo compounds by 1, 1′-bis (trimethylsilyl)-1 H, 1′ H-4, 4′-bipyridinylidene for giving alkenes and alkynes in a salt-free manner S Rej, S Pramanik, H Tsurugi, K Mashima Chemical Communications 53 (98), 13157-13160, 2017 | 29 | 2017 |
| Rhodiumkatalysierte sp2‐und sp3‐C‐H‐Funktionalisierungen mit entfernbaren dirigierenden Gruppen S Rej, N Chatani Angewandte Chemie 131 (25), 8390-8416, 2019 | 27 | 2019 |
| Pyrimidine-directed metal-free C–H borylation of 2-pyrimidylanilines: a useful process for tetra-coordinated triarylborane synthesis S Rej, A Das, N Chatani Chemical Science 12 (34), 11447-11454, 2021 | 26 | 2021 |
| Mixed Ligated Tris(amidinate)dimolybdenum Complexes as Catalysts for Radical Addition of CCl4 to 1-Hexene: Leaving Ligand Lability Controls Catalyst Activity S Rej, M Majumdar, S Kando, Y Sugino, H Tsurugi, K Mashima Inorganic Chemistry 56 (1), 634-644, 2017 | 25 | 2017 |
| Silylium-Ion-Promoted Hydrosilylation of Aryl-Substituted Allenes: Interception by Cyclization of the Allyl-Cation Intermediate S Rej, HFT Klare, M Oestreich Organic Letters 24 (6), 1346-1350, 2022 | 24 | 2022 |
| Rh (II)-catalyzed branch-selective C–H alkylation of aryl sulfonamides with vinylsilanes S Rej, N Chatani Chemical Science 11 (2), 389-395, 2020 | 24 | 2020 |
| Rhodium (I)-catalyzed mono-selective C–H alkylation of benzenesulfonamides with terminal alkenes S Rej, N Chatani Chemical Communications 55 (71), 10503-10506, 2019 | 22 | 2019 |
| Organosilicon reducing reagents for stereoselective formations of silyl enol ethers from α-halo carbonyl compounds S Pramanik, S Rej, S Kando, H Tsurugi, K Mashima The Journal of Organic Chemistry 83 (4), 2409-2417, 2018 | 21 | 2018 |
| Rhodium‐Catalyzed Alkylation of C‐H Bonds in Aromatic Amides with Unactivated 1‐Alkenes: The Possible Generation of Carbene Intermediates from Alkenes N Chatani, T Yamaguchi, S Natsui, K Shibata, K Yamazaki, S Rej, Y Ano Chemistry–A European Journal, 2019 | 17 | 2019 |
| RhIII‐Catalyzed Double Dehydrogenative Coupling of Free 1‐Naphthylamines with α,β‐Unsaturated Esters S Rej, N Chatani Chemistry–A European Journal 26 (49), 11093-11098, 2020 | 16 | 2020 |
Amrita DasTU Chemnitz (Postdoc), Osaka University (Postdoc), UTokyo (Postdoc)Overená e-mailová adresa na: chem.eng.osaka-u.ac.jp
