Keary Mark Engle, Ph.D., D.Phil.
Affiliations: | Chemistry | Scripps Research Institute, La Jolla, La Jolla, CA, United States |
Area:
organic synthesis, organometallics, catalysisWebsite:
www.englelab.comGoogle:
"Keary Engle"Mean distance: 6.69 | S | N | B | C | P |
Parents
Sign in to add mentorAdam J. Matzger | research assistant | 2003-2007 | University of Michigan |
Manfred T. Reetz | research assistant | 2007-2008 | Max-Planck-Institut für Kohlenforschung |
John M. Brown | grad student | 2008-2011 | Oxford |
Jin-Quan Yu | grad student | 2008-2011 | Scripps Institute |
Véronique Gouverneur | grad student | 2011-2013 | Oxford |
Robert Howard Grubbs | post-doc | 2013-2015 | Caltech |
Children
Sign in to add traineeShao-Xiong Lennon Luo | research assistant | 2014-2015 | Caltech |
Joseph Derosa | grad student | 2015-2020 | Scripps Institute |
John A. Gurak, Jr. | grad student | 2015-2020 | Scripps Institute |
Zhen Liu | grad student | 2015-2020 | Scripps Institute |
Miriam O'Duill | post-doc | 2015- | Scripps Institute |
Kin S. Yang | post-doc | 2015- | Scripps Institute |
Jose M. Medina | post-doc | 2018- | Scripps Institute |
De-Wei Gao | post-doc | 2016-2018 | Scripps Institute |
Sri Krishna Nimmagadda | post-doc | 2017-2018 | Scripps Institute |
Malkanthi K. Karunananda | post-doc | 2017-2022 | The Scripps Research Institute, La Jolla, CA |
Amit Kumar Simlandy | post-doc | 2021-2023 | The Scripps Research Institute, La Jolla, CA |
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Publications
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Rubel CZ, He WJ, Wisniewski SR, et al. (2024) Benchtop Nickel Catalysis Invigorated by Electron-Deficient Diene Ligands. Accounts of Chemical Research |
Laudadio G, Neigenfind P, Péter Á, et al. (2024) Nickel-Electrocatalytic Decarboxylative Arylation to Access Quaternary Centers. Angewandte Chemie (International Ed. in English). e202314617 |
Rubel CZ, Cao Y, El-Hayek Ewing T, et al. (2023) Electroreductive Synthesis of Nickel(0) Complexes. Angewandte Chemie (International Ed. in English). e202311557 |
Hwang Y, Wisniewski SR, Engle KM. (2023) Ligand-Enabled Carboamidation of Unactivated Alkenes through Enhanced Organonickel Electrophilicity. Journal of the American Chemical Society. 145: 25293-25303 |
Ni HQ, Dai JC, Yang S, et al. (2023) Catalytic σ-Bond Annulation with Ambiphilic Organohalides Enabled by β-X Elimination. Angewandte Chemie (International Ed. in English). e202306581 |
Ni HQ, Karunananda MK, Zeng T, et al. (2023) Redox-Paired Alkene Difunctionalization Enables Skeletally Divergent Synthesis. Journal of the American Chemical Society |
Simlandy AK, Alturaifi TM, Nguyen JM, et al. (2023) Enantioselective Hydroalkenylation and Hydroalkynylation of Alkenes Enabled by a Transient Directing Group: Catalyst Generality through Rigidification. Angewandte Chemie (International Ed. in English). e202304013 |
Gao Y, Kim N, Mendoza SD, et al. (2022) (CAAC)Copper Catalysis Enables Regioselective Three-Component Carboboration of Terminal Alkynes. Acs Catalysis. 12: 7243-7247 |
Tran VT, Kim N, Rubel CZ, et al. (2022) Structurally Diverse Bench-Stable Nickel(0) Pre-Catalysts: A Practical Toolkit for In Situ Ligation Protocols. Angewandte Chemie (International Ed. in English) |
Apolinar O, Kang T, Alturaifi TM, et al. (2022) Three-Component Asymmetric Ni-Catalyzed 1,2-Dicarbofunctionalization of Unactivated Alkenes via Stereoselective Migratory Insertion. Journal of the American Chemical Society |