Jacob T. Edwards
Affiliations: | 2012-2014 | Medicinal Chemistry | University of Minnesota, Twin Cities, Minneapolis, MN |
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Publications
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Merchant RR, Edwards JT, Qin T, et al. (2018) Modular radical cross-coupling with sulfones enables access to sp-rich (fluoro)alkylated scaffolds. Science (New York, N.Y.) |
Widen JC, Kempema AM, Baur JW, et al. (2018) Helenalin Analogues Targeting NF-κB p65: Thiol Reactivity and Cellular Potency Studies of Varied Electrophiles. Chemmedchem |
Widen JC, Kempema AM, Baur JW, et al. (2018) Front Cover: Helenalin Analogues Targeting NF-κB p65: Thiol Reactivity and Cellular Potency Studies of Varied Electrophiles (ChemMedChem 4/2018) Chemmedchem. 13: 288-288 |
Lo JC, Kim D, Pan CM, et al. (2017) Fe-Catalyzed C-C Bond Construction from Olefins via Radicals. Journal of the American Chemical Society |
Qin T, Malins LR, Edwards JT, et al. (2016) Nickel-Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms. Angewandte Chemie (International Ed. in English) |
Yan M, Lo JC, Edwards JT, et al. (2016) Radicals: Reactive Intermediates with Translational Potential. Journal of the American Chemical Society |
Wang J, Qin T, Chen TG, et al. (2016) Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids. Angewandte Chemie (International Ed. in English) |
Qin T, Cornella J, Li C, et al. (2016) A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents. Science (New York, N.Y.) |
Cornella J, Edwards JT, Qin T, et al. (2016) Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters. Journal of the American Chemical Society |