| Transition-metal-catalyzed C–N bond forming reactions using organic azides as the nitrogen source: a journey for the mild and versatile C–H amination K Shin, H Kim, S Chang Accounts of chemical research 48 (4), 1040-1052, 2015 | 894 | 2015 |
| Reductive Electrophotocatalysis: Merging Electricity and Light to Achieve Extreme Reduction Potentials H Kim, H Kim, TH Lambert, S Lin Journal of the American Chemical Society, 2020 | 322 | 2020 |
| Transition-metal-mediated direct C–H amination of hydrocarbons with amine reactants: the most desirable but challenging C–N bond-formation approach H Kim, S Chang Acs Catalysis 6 (4), 2341-2351, 2016 | 273 | 2016 |
| Iridium-catalyzed C–H amination with anilines at room temperature: compatibility of iridacycles with external oxidants H Kim, K Shin, S Chang Journal of the American Chemical Society 136 (16), 5904-5907, 2014 | 205 | 2014 |
| Copper-mediated selective cyanation of indoles and 2-phenylpyridines with ammonium iodide and DMF J Kim, H Kim, S Chang Organic letters 14 (15), 3924-3927, 2012 | 133 | 2012 |
| Copper-mediated amination of aryl C–H bonds with the direct use of aqueous ammonia via a disproportionation pathway H Kim, J Heo, J Kim, MH Baik, S Chang Journal of the American Chemical Society 140 (43), 14350-14356, 2018 | 94 | 2018 |
| The use of ammonia as an ultimate amino source in the transition metal-catalyzed C–H amination H Kim, S Chang Accounts of Chemical Research 50 (3), 482-486, 2017 | 94 | 2017 |
| A facile access to primary alkylamines and anilines via Ir (III)-catalyzed C–H amidation using azidoformates H Kim, G Park, J Park, S Chang ACS Catalysis 6 (9), 5922-5929, 2016 | 88 | 2016 |
| Synthesis of phosphoramidates: a facile approach based on the C–N bond formation via Ir-catalyzed direct C–H amidation H Kim, J Park, JG Kim, S Chang Organic letters 16 (20), 5466-5469, 2014 | 79 | 2014 |
| Iridium-catalyzed direct C–H amination with alkylamines: facile oxidative insertion of amino group into iridacycle H Kim, S Chang ACS Catalysis 5 (11), 6665-6669, 2015 | 74 | 2015 |
| Electrocatalytic access to azetidines via intramolecular allylic hydroamination: scrutinizing key oxidation steps through electrochemical kinetic analysis SH Park, G Bae, A Choi, S Shin, K Shin, CH Choi, H Kim Journal of the American Chemical Society 145 (28), 15360-15369, 2023 | 29 | 2023 |
| Electrocatalytic radical-polar crossover hydroetherification of alkenes with phenols SH Park, J Jang, K Shin, H Kim ACS Catalysis 12 (17), 10572-10580, 2022 | 29 | 2022 |
| Electrochemically driven stereoselective approach to syn-1, 2-diol derivatives from vinylarenes and DMF DS Chung, SH Park, S Lee, H Kim Chemical Science 12 (16), 5892-5897, 2021 | 27 | 2021 |
| Alternating current electrolysis: a photoredox catalysis mimic and beyond J Zhong, C Ding, H Kim, T McCallum, K Ye Green Synthesis and Catalysis 3 (1), 4-10, 2022 | 23 | 2022 |
| Reductive Electrosynthesis: A New Dawn SH Park, M Ju, AJ Ressler, J Shim, H Kim, S Lin Aldrichimica Acta 54 (1), 17-27, 2021 | 21 | 2021 |
| Radical hydrodifluoromethylation of unsaturated C− C bonds via an electroreductively triggered two-pronged approach S Kim, KH Hwang, HG Park, J Kwak, H Lee, H Kim Communications Chemistry 5 (1), 96, 2022 | 11 | 2022 |
| Palladium-Catalyzed electrooxidative hydrofluorination of aryl-substituted alkenes with a nucleophilic fluorine source A Mandal, J Jang, B Yang, H Kim, K Shin Organic Letters 25 (1), 195-199, 2022 | 9 | 2022 |
| Synthesis of 1H-Indazoles via Silver(I)-Mediated Intramolecular Oxidative C–H Bond Amination A Park, KS Jeong, H Lee, H Kim ACS omega 6 (9), 6498-6508, 2021 | 9 | 2021 |
| Electrocatalytic Radical-Polar Crossover Hydrofunctionalization of Alkenes via Cobalt-Catalyzed Hydrogen Atom Transfer A Choi, H Kim Current Opinion in Electrochemistry, 101449, 2024 | 2 | 2024 |
| Cu-Electrocatalysis Enables Vicinal Bis(difluoromethylation) of Alkenes: Unraveling Dichotomous Role of Zn(CF2H)2(DMPU)2 as Both Radical and Anion Source S Kim, H Kim Journal of the American Chemical Society, 2024 | | 2024 |
Sukbok ChangInstitute for Basic Science (IBS) and KAIST在 kaist.ac.kr 的电子邮件经过验证
