107. Transferable enantioselectivity models from sparse data

107. "Transferable enantioselectivity models from sparse data" Gallarati, S.; Bucci, E. M.; Doyle, A. G.; Sigman, M. S. Nature, Accelerated Preview. [DOI: 10.1038/s41586-026-10239-7] Link PDF

107. Transferable enantioselectivity models from sparse data2026-02-18T09:33:11-08:00

105. Development, Application, and Mechanistic Interrogation of a Dual Ni Catalysis Approach to Photoredox-Based C(sp3)–C(sp3) Cross-Coupling

105. "Development, Application, and Mechanistic Interrogation of a Dual Ni Catalysis Approach to Photoredox-Based C(sp3)–C(sp3) Cross-Coupling" Bucci, E. M.; Perea, M. A.; Lalisse, R. F.; Mukherjee, P.; Raab, T. J.; Kannadi Valloli, L.; Min, D. S.; Bird, M. J.; Gutierrez, O.; Doyle, A. G. J. Am. Chem. Soc., 2025, 147, 42311–42329. [DOI: 10.1021/jacs.5c11247] Link PDF

105. Development, Application, and Mechanistic Interrogation of a Dual Ni Catalysis Approach to Photoredox-Based C(sp3)–C(sp3) Cross-Coupling2026-01-27T16:48:15-08:00

102. Reactivity Studies of Bipyridine-Ligated Nickel(I) and Nickel(0) Complexes Inform the Mechanism in Modern Cross-Coupling Reactions

"Reactivity Studies of Bipyridine-Ligated Nickel(I) and Nickel(0) Complexes Inform the Mechanism in Modern Cross-Coupling Reactions" Raab, T. Judah.; Doyle, A. G. J. Am. Chem. Soc., 2025, 147, 33991–34000. [DOI: 10.1021/jacs.5c11247] Link PDF

102. Reactivity Studies of Bipyridine-Ligated Nickel(I) and Nickel(0) Complexes Inform the Mechanism in Modern Cross-Coupling Reactions2026-01-24T17:39:03-08:00

100. Ni-Catalyzed Reductive Coupling of Acetals with Anhydrides and Vinyl Triflates via Single-Electron C–O Activation

"Ni-Catalyzed Reductive Coupling of Acetals with Anhydrides and Vinyl Triflates via Single-Electron C–O Activation" Kim, E.; Borden, M. A.; Hwang, J.; Doyle, A. G.; Dongbang, S. Org. Lett., 2025, 27, 9454–9459. [DOI: 10.1021/acs.orglett.5c02788] Link PDF

100. Ni-Catalyzed Reductive Coupling of Acetals with Anhydrides and Vinyl Triflates via Single-Electron C–O Activation2025-09-08T08:57:08-07:00

97. Applying Active Learning toward Building a Generalizable Model for Ni-Photoredox Cross-Electrophile Coupling of Aryl and Alkyl Bromides

"Applying Active Learning toward Building a Generalizable Model for Ni-Photoredox Cross-Electrophile Coupling of Aryl and Alkyl Bromides" Souza, L. W.; Ricke, N. D.; Chaffin, B. C.; Fortunato, M. E.; Jiang, S.; Soylu, C.; Caya, T. C.; Lau, S. H.; Wieser, K. A.; Doyle, A. G.; Tan, K. L. J. Am. Chem. Soc., 2025, 147, 18747-18759.

97. Applying Active Learning toward Building a Generalizable Model for Ni-Photoredox Cross-Electrophile Coupling of Aryl and Alkyl Bromides2025-07-03T17:23:09-07:00

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 Alkenes2024-05-27T18:33:20-07:00
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