Ni Cross-Coupling – Page 2

84. Branched-Selective Cross-Electrophile Coupling of 2-Alkyl Aziridines and (Hetero)aryl Iodides Using Ti/Ni Catalysis

"Branched-Selective Cross-Electrophile Coupling of 2-Alkyl Aziridines and (Hetero)aryl Iodides Using Ti/Ni Catalysis" Williams, W. L.; Gutiérrez-Valencia, N. E.; Doyle, A. G. J. Am. Chem. Soc. 2023, 145, 24175-24183. [DOI: 10.1021/jacs.3c08301] Link PDF

84. Branched-Selective Cross-Electrophile Coupling of 2-Alkyl Aziridines and (Hetero)aryl Iodides Using Ti/Ni CatalysisFlora Fan2024-05-27T18:32:07-07:00

83. Synthesis of Nickel(I)–Bromide Complexes via Oxidation and Ligand Displacement: Evaluation of Ligand Effects on Speciation and Reactivity

"Synthesis of Nickel(I)–Bromide Complexes via Oxidation and Ligand Displacement: Evaluation of Ligand Effects on Speciation and Reactivity" Newman-Stonebraker, S. H.; Raab, T. J.; Roshandel, H. R.; Doyle, A. G. J. Am. Chem. Soc. 2023, 145, 19368-19377. [DOI: 10.1021/jacs.3c06233] Link PDF

83. Synthesis of Nickel(I)–Bromide Complexes via Oxidation and Ligand Displacement: Evaluation of Ligand Effects on Speciation and ReactivityDaniel Min2024-05-27T18:31:51-07:00

80. Comparison of Monophosphine and Bisphosphine Precatalysts for Ni-Catalyzed Suzuki–Miyaura Cross-Coupling: Understanding the Role of the Ligation State in Catalysis

Borowski, J. E.; Newman-Stonebraker, S. H.; Doyle, A. G. ACS. Catal. 2023, 13, 7966-7977. [DOI: 10.1021/acscatal.3c01331] Link PDF

80. Comparison of Monophosphine and Bisphosphine Precatalysts for Ni-Catalyzed Suzuki–Miyaura Cross-Coupling: Understanding the Role of the Ligation State in CatalysisFlora Fan2023-06-05T13:39:19-07:00

78. Interrogating the Mechanistic Features of Ni(I)-Mediated Aryl Iodide Oxidative Addition Using Electroanalytical and Statistical Modeling Techniques

Tang, T.; Hazra, A.; Min, D. S.; Williams, W. L.; Doyle, A. G.; Sigman M. S. J. Am. Chem. Soc. 2023, 145, 8689-8699. [DOI: 10.1021/jacs.3c01726] Link PDF

78. Interrogating the Mechanistic Features of Ni(I)-Mediated Aryl Iodide Oxidative Addition Using Electroanalytical and Statistical Modeling TechniquesDaniel Min2023-04-25T09:16:29-07:00

73. Ni/Photoredox-Catalyzed C(sp3)–C(sp3) Coupling between Aziridines and Acetals as Alcohol-Derived Alkyl Radical Precursors

Dongbang, S; Doyle, A. G. J. Am. Chem. Soc. 2022, 144, 20067–20077. [DOI: 10.1021/jacs.2c09294] Link PDF

73. Ni/Photoredox-Catalyzed C(sp3)–C(sp3) Coupling between Aziridines and Acetals as Alcohol-Derived Alkyl Radical PrecursorsWill Lau2022-12-30T17:42:21-08:00

72. Structure–Reactivity Relationships of Buchwald-Type Phosphines in Nickel-Catalyzed Cross-Couplings

Newman-Stonebraker, S. H.; Wang, J. Y.; Jeffrey P. D.; Doyle, A. G. J. Am. Chem. Soc. 2022, 144, 19635-19648. [DOI: 10.1021/jacs.2c09840] Link PDF

72. Structure–Reactivity Relationships of Buchwald-Type Phosphines in Nickel-Catalyzed Cross-CouplingsWill Lau2022-12-30T17:30:50-08:00

70. Oxidative Addition of Aryl Halides to a Ni(I)-Bipyridine Complex

Ting, S. I.; Williams, W. L.; Doyle, A. G. J. Am. Chem. Soc. 2022, 144, 5575-5582. [DOI: 10.1021/jacs.2c00462] Link PDF

70. Oxidative Addition of Aryl Halides to a Ni(I)-Bipyridine ComplexWill Lau2022-12-30T17:15:24-08:00

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

62. Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysis

Newman-Stonebraker, S. H.; Smith, S. R.; Borowski, J. E.; Peters, E.; Gensch, T.; Johnson, H. C.; Sigman, M. S.; Doyle, A. G. Science 2021, 374, 301-308. [DOI: 10.1126/science.ajb4213] Link PDF

62. Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysisWill Lau2022-12-30T16:48:28-08:00

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