David Charboneau
Affiliations: | 2019- | Chemistry | California Institute of Technology, Pasadena, CA |
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"David Charboneau"Parents
Sign in to add mentorJared J. Paul | research assistant | 2015 | Villanova |
Nilay Hazari | grad student | 2016-2021 | Yale |
Sarah E. Reisman | post-doc | 2021- | Caltech |
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Publications
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Boyd EA, Shin C, Charboneau DJ, et al. (2024) Reductive samarium (electro)catalysis enabled by Sm-alkoxide protonolysis. Science (New York, N.Y.). 385: 847-853 |
Charboneau DJ, Huang H, Barth EL, et al. (2024) Homogeneous Organic Reductant Based on 4,4'-Bu-2,2'-Bipyridine for Cross-Electrophile Coupling. Tetrahedron Letters. 145 |
Ware SD, Zhang W, Charboneau DJ, et al. (2023) Electrochemical Preparation of Sm(II) Reagent Facilitated by Weakly Coordinating Anions. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301045 |
Charboneau DJ, Hazari N, Huang H, et al. (2022) Homogeneous Organic Electron Donors in Nickel-Catalyzed Reductive Transformations. The Journal of Organic Chemistry. 87: 7589-7609 |
Reed-Lingenfelter SN, Chen Y, Yarali M, et al. (2022) Compact Super Electron-Donor to Monolayer MoS. Nano Letters |
Deziel AP, Espinosa MR, Pavlovic L, et al. (2022) Ligand and solvent effects on CO insertion into group 10 metal alkyl bonds. Chemical Science. 13: 2391-2404 |
Charboneau DJ, Huang H, Barth EL, et al. (2021) Tunable and Practical Homogeneous Organic Reductants for Cross-Electrophile Coupling. Journal of the American Chemical Society |
Edington SC, Perez EH, Charboneau DJ, et al. (2021) Chemical Reduction of Ni Cyclam and Characterization of Isolated Ni Cyclam with Cryogenic Vibrational Spectroscopy and Inert-Gas-Mediated High-Resolution Mass Spectrometry. The Journal of Physical Chemistry. A |
Charboneau DJ, Barth EL, Hazari N, et al. (2020) A Widely Applicable Dual Catalytic System for Cross-Electrophile Coupling Enabled by Mechanistic Studies. Acs Catalysis. 10: 12642-12656 |
Charboneau DJ, Brudvig GW, Hazari N, et al. (2019) Development of an Improved System for the Carboxylation of Aryl Halides through Mechanistic Studies. Acs Catalysis. 9: 3228-3241 |