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

Affiliations: 
Chemistry Scripps Research Institute, La Jolla, La Jolla, CA, United States 
Area:
organic synthesis, organometallics, catalysis
Website:
www.englelab.com
Google:
"Keary Engle"
Mean distance: 6.69
 
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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
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