85. Dataset Design for Building Models of Chemical Reactivity

"Dataset Design for Building Models of Chemical Reactivity" Raghavan, P; Haas, B. C.; Ruos, M. E.; Schleinitz, J; Doyle, A. G.; Reisman, S. E.; Sigman, M. S.; Coley, C. W. J. Am. Chem. Soc. 2023, 145, 24175-24183. [DOI: 10.1021/jacs.3c08301] Link PDF

85. Dataset Design for Building Models of Chemical Reactivity2024-05-27T18:32:22-07:00

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 Catalysis2024-05-27T18:32:07-07:00

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 Reactivity2024-05-27T18:31:51-07:00

81. Continuous flow synthesis of pyridinium salts accelerated by multi-objective Bayesian optimization with active learning

"Continuous flow synthesis of pyridinium salts accelerated by multi-objective Bayesian optimization with active learning" Dunlap, J. H.; Ethier, J. G.; Putnam-Neeb, A. A.; Iyer, S.; Luo, S.-X. L.; Feng, H.; Torres, J. A. G.; Doyle, A. G.; Swager, T. M.; Vaia, R. A.; Mirau, P.; Crouse, C. A.; Baldwin, L. A. Chem. Sci. 2023, 14, 8061-8069.

81. Continuous flow synthesis of pyridinium salts accelerated by multi-objective Bayesian optimization with active learning2024-05-27T18:31:12-07:00

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 Catalysis2023-06-05T13:39:19-07:00

The Doyle Lab • Prof. Abigail Doyle
Saul Winstein Chair in Organic Chemistry
Department of Chemistry and Biochemistry, UCLA
3515 Molecular Science Building • Los Angeles, CA 90095
abigaildoyle@g.ucla.edu • Phone: (310) 206-1036

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