Ni Cross-Coupling – Page 2

89. Data Science Guided Multiobjective Optimization of a Stereoconvergent Nickel-Catalyzed Reduction of Enol Tosylates to Access Trisubstituted Alkenes

"Data Science Guided Multiobjective Optimization of a Stereoconvergent Nickel-Catalyzed Reduction of Enol Tosylates to Access Trisubstituted Alkenes" Romer, N. P.; Min, D. S.; Wang, J. Y.; Walroth, R. C.; Mack, K. A.; Sirois, L. E.; Gosselin, F.; Zell, D.; Doyle, A. G.; Sigman, M. S. ACS Catal, 2024, 14, 4699-4708. [DOI: 10.1021/acscatal.4c00650] Link PDF

89. Data Science Guided Multiobjective Optimization of a Stereoconvergent Nickel-Catalyzed Reduction of Enol Tosylates to Access Trisubstituted AlkenesFlora Fan2024-05-27T18:33:20-07:00

86. Catalyst Deactivation of a Monoligated CyJohnPhos-Bound Nickel(0) Complex

"Catalyst Deactivation of a Monoligated CyJohnPhos-Bound Nickel(0) Complex" Newman-Stonebraker, S. H.; Raab, T. J.; Doyle, A. G. Organometallics 2023, 42, 3438-3441. [DOI: 10.1021/jacs.3c08301] Link PDF

86. Catalyst Deactivation of a Monoligated CyJohnPhos-Bound Nickel(0) ComplexFlora Fan2024-05-27T18:32:36-07:00

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