41. Ni-Catalyzed Carbon-Carbon Bond-Forming Reductive Amination
Heinz, C.; Lutz, J. P.; Simmons, E. M.; Miller, M. M.; Ewing, W. R.; Doyle, A. G. J. Am. Chem. Soc. 2018, 140, 2292-2300. [DOI: 10.1021/jacs.7b12212] Link PDF
40. Mild, Redox-Neutral Formylation of Aryl Chlorides via Photocatalytic Generation of Chlorine radicals
Nielsen, M. K.; Shields, B. J.; Liu, J. Williams, M. J.; Zacuto, M. J; Doyle, A. G. Angew. Chem. Int. Ed. 2017, 56, 7191-7194. [DOI: 10.1002/ange.201702079] Link PDF
39. Nickel-Catalyzed Enantioselective Reductive Cross-Coupling of Styrenyl Aziridines
Woods, B. P.; Orlandi, M.; Huang, C.-Y. Sigman, M. H.; Doyle, A. G. J. Am. Chem. Soc. 2017, 139, 5688-5691. [DOI: 10.1021/jacs.7b03448] Link PDF
38. Nickel-photoredox catalyzed enantioselective desymmetrization of meso cyclic anhydrides
Angew. Chem. Int. Ed. J. Am. Chem. Soc. 2017, 56, 3679-3683. [DOI:10.1002/anie.201700097] Link PDF
37. Parameterization of phosphine ligands demonstrates enhancement of nickel catalysis via remote steric effects
Wu, K.; Doyle, A. G. Nature Chem. 2017, 9, 779-784. [DOI:10.1038/nchem.2741] Link PDF
36. Direct C(sp3)−H Cross Coupling Enabled by Catalytic Generation of Chlorine Radicals
Shields, B. J.; Doyle, A. G. J. Am. Chem. Soc. 2016, 138, 12719−12722. [DOI: 10.1021/jacs.6b08397] Link PDF
34. C–H functionalization of amines with aryl halides by nickel-photoredox catalysis
Ahneman, D. T.; Doyle, A. G. Chem. Sci. 2016, 7, 7002-7006. [DOI:10.1039/C6SC02815B] Link PDF
33. Nickel-catalyzed enantioselective arylation of pyridine
Lutz, J. P.; Chau, S. T.; Doyle, A. G. Chem. Sci. 2016, 7, 4105-4109. [DOI: 10.1039/C6SC00702C] Link PDF
32. Direct Acylation of C(sp3)−H Bonds Enabled by Nickel and Photoredox Catalysis
Joe, C. L.; Doyle, A. G. Angew. Chem. Int. Ed. 2016, 55, 4040-4043. [DOI: 10.1002/anie.201511438] Link PDF
30. Dialkyl Ether Formation via Nickel-Catalyzed Cross Coupling of Acetals and Aryl Iodides
Arendt, K. M.; Doyle, A. G. Angew. Chem. Int. Ed. 2015, 54, 9876-9880. [DOI: 10.1002/anie.201503936] Link PDF
