Photocatalysis – Page 2 – The Doyle Group

68. Using Data Science to Guide Aryl Bromide Substrate Scope Analysis in a Ni/Photoredox-Catalyzed Cross-Coupling with Acetals as Alcohol-Derived Radical Sources

Kariofillis, S. K.; Jiang, S.; Żurański, A. M.; Gandhi, S. S.; Martinez Alvarado, J. I.; Doyle, A. G. J. Am. Chem. Soc. 2022, 144, 1045-1055. [DOI: 10.1021/jacs.1c12203] Link PDF

68. Using Data Science to Guide Aryl Bromide Substrate Scope Analysis in a Ni/Photoredox-Catalyzed Cross-Coupling with Acetals as Alcohol-Derived Radical SourcesWill Lau2022-12-30T17:04:00-08:00

67. A General Strategy for C(sp3)–H Functionalization with Nucleophiles Using Methyl Radical as a Hydrogen Atom Abstractor

Leibler, I. N.-M.; Tekle-Smith, M. A.; Doyle, A. G. Nat. Commun. 2021, 12, 6950. [DOI: 10.1038/s41467-021-27165-z] Link PDF

67. A General Strategy for C(sp3)–H Functionalization with Nucleophiles Using Methyl Radical as a Hydrogen Atom AbstractorWill Lau2022-12-30T17:01:58-08:00

66. A Biohybrid Strategy for Enabling Photoredox Catalysis with Low-Energy Light

Cesana, P. T.; Li, B. X.; Shepard, S. G.; Ting, S. I.; Hart, S. M.; Olson, C. M.; Martinez Alvarado, J. I.; Son, M.; Steiman, T. J.; Castellano, F. N.; Doyle, A. G.; MacMillan, D. W. C.; Schlau-Cohen, G. S. Chem. 2021, 8, 174-185. [DOI: 10.1016/j.chempr.2021.10.010] Link PDF

66. A Biohybrid Strategy for Enabling Photoredox Catalysis with Low-Energy LightWill Lau2022-12-30T20:32:18-08:00

63. Phosphine/Photoredox Catalyzed Anti-Markovnikov Hydroamination of Olefins with Primary Sulfonamides via α-Scission from Phosphoranyl Radicals

Chinn, A. J.; Sedillo, K.; Doyle, A. G. J. Am. Chem. Soc. 2021, 143, 18331-18338. [DOI: 10.1021/jacs.1c09484] Link PDF

63. Phosphine/Photoredox Catalyzed Anti-Markovnikov Hydroamination of Olefins with Primary Sulfonamides via α-Scission from Phosphoranyl RadicalsWill Lau2022-12-30T20:30:50-08:00

61. Ni/Photoredox-Catalyzed Enantioselective Cross-Electrophile Coupling of Styrene Oxides with Aryl Iodides

Lau, S. H.; Borden, M. A.; Steiman, T. J.; Parasram, M.; Wang, L. S.; Doyle, A. G. J. Am. Chem. Soc. 2021, 143, 15873-15881. [DOI: 10.1021/jacs.1c08105] Link PDF

61. Ni/Photoredox-Catalyzed Enantioselective Cross-Electrophile Coupling of Styrene Oxides with Aryl IodidesWill Lau2022-12-30T16:44:26-08:00

57. Synthetic and Mechanistic Implications of Chlorine Photoelimination in Nickel/Photoredox C(sp3)–H Cross-Coupling

Kariofillis, S. K.; Doyle, A. G. Acc. Chem. Res. 2021, 54, 988-1000. [DOI: 10.1021/acs.accounts.0c00694] Link PDF

57. Synthetic and Mechanistic Implications of Chlorine Photoelimination in Nickel/Photoredox C(sp3)–H Cross-CouplingWill Lau2022-12-30T20:34:14-08:00

56. Bioinspiration in Light Harvesting and Catalysis

Proppe, A. H.; Li, Y. C.; Aspuru-Guzik, A.; Berlinguette, C. P.; Chang, C. J.; Cogdell, R.; Doyle, A. G.; Flick, J.; Gabor, N. M.; van Grondelle, R.; Hammes-Schiffer, S.; Jaffer, S. A.; Kelley, S. O.; Leclerc, M.; Leo, K.; Mallouk, T. E.; Narang, P.; Schlau-Cohen, G. S.; Scholes, G. D.; Vojvodic, A.; Yam, V. W.;

56. Bioinspiration in Light Harvesting and CatalysisWill Lau2022-12-30T20:35:01-08:00

54. Regioselective Cross-Electrophile Coupling of Epoxides and (Hetero)aryl Iodides via Ni/Ti/Photoredox Catalysis

Parasram, M.; Shields, B. J.; Ahmad, O.; Knauber, T.; Doyle, A. G. ACS Catal. 2020, 10, 5821-5827. [DOI: 10.1021/acscatal.0c01199] Link PDF

54. Regioselective Cross-Electrophile Coupling of Epoxides and (Hetero)aryl Iodides via Ni/Ti/Photoredox Catalysisjamie2022-12-30T16:17:21-08:00

52. Nickel/Photoredox-Catalyzed Methylation of (Hetero)aryl Chlorides Using Trimethyl Orthoformate as a Methyl Radical Source

Kariofillis, S. K.; Shields, B. J.; Tekle-Smith, M. A.; Zacuto, M. J.; Doyle, A. G. J. Am. Chem. Soc. 2020, 142, 7683-7689. [DOI: 10.1021/jacs.0c02805] Link PDF

52. Nickel/Photoredox-Catalyzed Methylation of (Hetero)aryl Chlorides Using Trimethyl Orthoformate as a Methyl Radical Sourcejamie2022-12-30T16:13:51-08:00

51. Synthesis of β-Phenethylamines via Ni/Photoredox Cross-Electrophile Coupling of Aliphatic Aziridines and Aryl Iodides

Steiman, T. J.; Liu, J.; Mengiste, A.; Doyle, A. G. J. Am. Chem. Soc. 2020, 142, 7598-7605. [DOI: 10.1021/jacs.0c01724] Link PDF

51. Synthesis of β-Phenethylamines via Ni/Photoredox Cross-Electrophile Coupling of Aliphatic Aziridines and Aryl Iodidesjamie2022-12-30T16:13:22-08:00