| Recent developments in nickel-catalyzed intermolecular dicarbofunctionalization of alkenes J Derosa, O Apolinar, T Kang, VT Tran, KM Engle Chemical Science 11 (17), 4287-4296, 2020 | 315 | 2020 |
| Nickel‐catalyzed 1, 2‐diarylation of alkenyl carboxylates: a gateway to 1, 2, 3‐trifunctionalized building blocks J Derosa, T Kang, VT Tran, SR Wisniewski, MK Karunananda, TC Jankins, ... Angewandte Chemie International Edition 59 (3), 1201-1205, 2020 | 71 | 2020 |
| Nickel-catalyzed 1, 2-carboamination of alkenyl alcohols T Kang, N Kim, PT Cheng, H Zhang, K Foo, KM Engle Journal of the American Chemical Society 143 (34), 13962-13970, 2021 | 62 | 2021 |
| Cyclic (Alkyl)(amino) carbene Ligands Enable Cu‐Catalyzed Markovnikov Protoboration and Protosilylation of Terminal Alkynes: A Versatile Portal to Functionalized Alkenes Y Gao, S Yazdani, A Kendrick IV, GP Junor, T Kang, DB Grotjahn, ... Angewandte Chemie International Edition 60 (36), 19871-19878, 2021 | 46 | 2021 |
| Design, synthesis, and biological evaluation of C7-functionalized DMXAA derivatives as potential human-STING agonists J Hwang, T Kang, J Lee, BS Choi, S Han Organic & biomolecular chemistry 17 (7), 1869-1874, 2019 | 40 | 2019 |
| Three-component asymmetric Ni-catalyzed 1, 2-dicarbofunctionalization of unactivated alkenes via stereoselective migratory insertion O Apolinar, T Kang, TM Alturaifi, PG Bedekar, CZ Rubel, J Derosa, ... Journal of the American Chemical Society 144 (42), 19337-19343, 2022 | 28 | 2022 |
| Electrophilic Sulfur Reagent Design Enables Directed syn-Carbosulfenylation of Unactivated Alkenes ZQ Li, Y Cao, T Kang, KM Engle Journal of the American Chemical Society 144 (16), 7189-7197, 2022 | 28 | 2022 |
| Alkene difunctionalization directed by free amines: Diamine synthesis via nickel-catalyzed 1, 2-carboamination T Kang, JM González, ZQ Li, K Foo, PTW Cheng, KM Engle ACS Catalysis 12 (7), 3890-3896, 2022 | 25 | 2022 |
| Structurally Diverse Bench‐Stable Nickel (0) Pre‐Catalysts: A Practical Toolkit for In Situ Ligation Protocols VT Tran, N Kim, CZ Rubel, X Wu, T Kang, TC Jankins, ZQ Li, MV Joannou, ... Angewandte Chemie 135 (9), e202211794, 2023 | 24 | 2023 |
| Multifaceted substrate–ligand interactions promote the copper-catalyzed hydroboration of benzylidenecyclobutanes and related compounds T Kang, TG Erbay, KL Xu, GM Gallego, A Burtea, SK Nair, RL Patman, ... ACS catalysis 10 (21), 13075-13083, 2020 | 21 | 2020 |
| Cu-Catalyzed Hydroboration of Benzylidenecyclopropanes: Reaction Optimization,(Hetero) Aryl Scope, and Origins of Pathway Selectivity JM Medina, T Kang, TG Erbay, H Shao, GM Gallego, S Yang, ... ACS catalysis 9 (12), 11130-11136, 2019 | 21 | 2019 |
| Six-step total synthesis of azaspirene T Kang, D Jo, S Han The Journal of Organic Chemistry 82 (18), 9335-9341, 2017 | 16 | 2017 |
| An under-appreciated source of reproducibility issues in cross-coupling: solid-state decomposition of primary sodium alkoxides in air R Wethman, J Derosa, VT Tran, T Kang, O Apolinar, A Abraham, ... ACS Catalysis 11 (2), 502-508, 2020 | 13 | 2020 |
| Asymmetric Reductive Dicarbofunctionalization of Alkenes via Nickel Catalysis D Anthony, T Diao Synlett 31 (15), 1443-1447, 2020 | 12 | 2020 |
| Ni-and Pd-Catalyzed Enantioselective 1, 2-Dicarbofunctionalization of Alkenes T Kang, O Apolinar, KM Engle Synthesis, 2023 | 9 | 2023 |
| Synthesis and Characterization of Post-β-Carbon-Elimination Organopalladium Complexes T Kang, Y Fu, R Li-Matsuura, AL Liu, TC Jankins, AL Rheingold, JB Bailey, ... Organometallics 42 (1), 11-15, 2022 | 3 | 2022 |
| Metal-Mediated and Catalyzed Difunctionalization of Unsaturated Organics LJ Oxtoby, AM Vasquez, T Kang, ZQ Li, KM Engle Elsevier, 2022 | 2 | 2022 |
| Electrophilic Sulfur Reagent Design Enables Catalytic Syn-Carbosulfenylation of Unactivated Alkenes ZQ Li, Y Cao, T Kang, K Engle | 1 | 2021 |
| Nickel-catalyzed 1, 2-Difunctionalization of Unactivated Alkenes Directed by Native Functional Groups T Kang Scripps Research Institute, 2023 | | 2023 |
| rsc. li/chemical-science J Derosa, O Apolinar, T Kang, VT Tran, KM Engle, E Brunner, M Rauche | | |
Keary M. EngleProfessor, The Scripps Research Institute在 scripps.edu 的电子邮件经过验证
