Selective carbon–carbon bond cleavage of cyclopropanols TR McDonald, LR Mills, MS West, SAL Rousseaux Chemical Reviews 121 (1), 3-79, 2020 | 184 | 2020 |
Ni-catalyzed reductive cyanation of aryl halides and phenol derivatives via transnitrilation LR Mills, JM Graham, P Patel, SAL Rousseaux Journal of the American Chemical Society 141 (49), 19257-19262, 2019 | 85 | 2019 |
Modern developments in the chemistry of homoenolates LR Mills, SAL Rousseaux European Journal of Organic Chemistry 2019 (1), 8-26, 2019 | 72 | 2019 |
Ni-catalyzed β-alkylation of cyclopropanol-derived homoenolates LR Mills, C Zhou, E Fung, SAL Rousseaux Organic letters 21 (21), 8805-8809, 2019 | 63 | 2019 |
Electrophilic zinc homoenolates: synthesis of cyclopropylamines from cyclopropanols and amines LR Mills, LM Barrera Arbelaez, SAL Rousseaux Journal of the American Chemical Society 139 (33), 11357-11360, 2017 | 61 | 2017 |
The Cyclopropane Ring as a Reporter of Radical Leaving-Group Reactivity for Ni-Catalyzed C(sp3)–O Arylation LR Mills, JJ Monteith, G dos Passos Gomes, A Aspuru-Guzik, ... Journal of the American Chemical Society 142 (30), 13246-13254, 2020 | 43 | 2020 |
Design of an electron-withdrawing benzonitrile ligand for Ni-catalyzed cross-coupling involving tertiary nucleophiles LR Mills, RK Edjoc, SAL Rousseaux Journal of the American Chemical Society 143 (27), 10422-10428, 2021 | 34 | 2021 |
Cobalt-Catalyzed C(sp2)–C(sp3) Suzuki–Miyaura Cross-Coupling Enabled by Well-Defined Precatalysts with L,X-Type Ligands LR Mills, D Gygi, JR Ludwig, EM Simmons, SR Wisniewski, J Kim, ... ACS catalysis 12 (3), 1905-1918, 2022 | 21 | 2022 |
Synthesis of trans-2-Substituted Cyclopropylamines from α-Chloroaldehydes MS West, LR Mills, TR McDonald, JB Lee, D Ensan, SAL Rousseaux Organic letters 21 (20), 8409-8413, 2019 | 14 | 2019 |
Mechanistic Investigations of Phenoxyimine–Cobalt(II)-Catalyzed C(sp2)–C(sp3) Suzuki–Miyaura Cross-Coupling LR Mills, D Gygi, EM Simmons, SR Wisniewski, J Kim, PJ Chirik Journal of the American Chemical Society 145 (31), 17029-17041, 2023 | 13 | 2023 |
A one-pot electrophilic cyanation–functionalization strategy for the synthesis of disubstituted malononitriles LR Mills, SAL Rousseaux Tetrahedron 75 (32), 4298-4306, 2019 | 11 | 2019 |
Boronic acid-mediated ring-opening and Ni-catalyzed arylation of 1-arylcyclopropyl tosylates LR Mills, JJ Monteith, SAL Rousseaux Chemical Communications 56 (83), 12538-12541, 2020 | 9 | 2020 |
Ni-Catalyzed Synthesis of Thiocarboxylic Acid Derivatives JJ Monteith, K Scotchburn, LR Mills, SAL Rousseaux Organic Letters 24 (2), 619-624, 2022 | 8 | 2022 |
Electrophilic Metal Homoenolates and Their Application in the Synthesis of Cyclopropylamines LR Mills, SAL Rousseaux Synlett 29 (06), 683-688, 2018 | 7 | 2018 |
Phenoxythiazoline (FTz)‐Cobalt(II) Precatalysts Enable C(sp2)–C(sp3) Bond‐Formation for Key Intermediates in the Synthesis of Toll‐like Receptor 7/8 … LR Mills, F Di Mare, D Gygi, H Lee, EM Simmons, J Kim, SR Wisniewski, ... Angewandte Chemie 135 (51), e202313848, 2023 | 1 | 2023 |
Decyanation–(hetero) arylation of malononitriles to access α-(hetero) arylnitriles LR Mills, P Patel, SAL Rousseaux Organic & Biomolecular Chemistry 20 (30), 5933-5937, 2022 | 1 | 2022 |
C(sp3)–C(sp3) Reductive Elimination from (Phenoxyimine)Cobalt(III)(CH3)2(PMe3)2 Complexes LR Mills, J Kim, EM Simmons, SR Wisniewski, PJ Chirik Organometallics 43 (9), 1021-1029, 2024 | | 2024 |
(Phenoxyimine)nickel-Catalyzed C(sp2)–C(sp3) Suzuki–Miyaura Cross-Coupling: Evidence for a Recovering Radical Chain Mechanism LR Mills, EM Simmons, H Lee, E Nester, J Kim, SR Wisniewski, ... Journal of the American Chemical Society 146 (14), 10124-10141, 2024 | | 2024 |
Phenoxythiazoline (FTz)–Cobalt (II) Precatalysts Enable C (sp2)–C (sp3) Bond–Formation for the Key Intermediate in the Synthesis of Afimetoran and Related Toll-like Receptor 7 … LR Mills, F DiMare, D Gygi, H Lee, EM Simmons, J Kim, SR Wisniewski, ... | | 2023 |
New Strategies for C–O and C–C Functionalization in the Contexts of Cyclopropanol Chemistry, Transnitrilation, and Ni Catalysis LR Mills University of Toronto (Canada), 2020 | | 2020 |