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The Journal of Organic Chemistry|June 7, 2022
Homogeneous Organic Electron Donors in Nickel-Catalyzed Reductive TransformationsDavid J Charboneau, Nilay Hazari, Haotian Huang, et al.
Science (New York, N.Y.)|August 22, 2024
Reductive samarium (electro)catalysis enabled by Sm<sup>III</sup>-alkoxide protonolysisEmily A Boyd, Chungkeun Shin, David J Charboneau, et al.
ACS Catalysis|February 25, 2021
A Widely Applicable Dual Catalytic System for Cross-Electrophile Coupling Enabled by Mechanistic StudiesDavid J Charboneau, Emily L Barth, Nilay Hazari, et al.
ACS Catalysis|April 23, 2019
Development of an Improved System for the Carboxylation of Aryl Halides through Mechanistic StudiesDavid J Charboneau, Gary W Brudvig, Nilay Hazari, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 13, 2023
Electrochemical Preparation of Sm(II) Reagent Facilitated by Weakly Coordinating AnionsSkyler D Ware, Wendy Zhang, David J Charboneau, et al.
Chemical Science|March 28, 2022
Ligand and solvent effects on CO<sub>2</sub> insertion into group 10 metal alkyl bondsAnthony P Deziel, Matthew R Espinosa, Ljiljana Pavlovic, et al.
Journal of the American Chemical Society|November 30, 2021
Tunable and Practical Homogeneous Organic Reductants for Cross-Electrophile CouplingDavid J Charboneau, Haotian Huang, Emily L Barth, et al.
Tetrahedron Letters|July 22, 2024
Homogeneous Organic Reductant Based on 4,4'-<sup>t</sup>Bu<sub>2</sub>-2,2'-Bipyridine for Cross-Electrophile CouplingDavid J Charboneau, Haotian Huang, Emily L Barth, et al.
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