Keary Mark Engle, Ph.D., D.Phil.

Chemistry Scripps Research Institute, La Jolla, La Jolla, CA, United States 
organic synthesis, organometallics, catalysis
"Keary Engle"
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Rubel CZ, Ravn AK, Ho HC, et al. (2024) Stereodivergent, Kinetically Controlled Isomerization of Terminal Alkenes via Nickel Catalysis. Angewandte Chemie (International Ed. in English). e202320081
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)
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