| Sulfonyl fluorides as targets and substrates in the development of new synthetic methods TSB Lou, MC Willis Nature Reviews Chemistry 6 (2), 146-162, 2022 | 178 | 2022 |
| Flow chemistry as a discovery tool to access sp 2–sp 3 cross-coupling reactions via diazo compounds DN Tran, C Battilocchio, SB Lou, JM Hawkins, SV Ley Chemical science 6 (2), 1120-1125, 2015 | 135 | 2015 |
| Cyclic Alkenylsulfonyl Fluorides: Palladium‐Catalyzed Synthesis and Functionalization of Compact Multifunctional Reagents TSB Lou, SW Bagley, MC Willis Angewandte Chemie 131 (52), 19035-19039, 2019 | 95 | 2019 |
| Scalable, Chemoselective Nickel Electrocatalytic Sulfinylation of Aryl Halides with SO2 TSB Lou, Y Kawamata, T Ewing, GA Correa‐Otero, MR Collins, PS Baran Angewandte Chemie International Edition 61 (37), e202208080, 2022 | 58 | 2022 |
| Arylsulfonyl fluoride boronic acids: Preparation and coupling reactivity TSB Lou, MC Willis Tetrahedron 76 (1), 130782, 2020 | 21 | 2020 |
| Stock solution of SO2 as practical reagent for Ni-electrocatalytic sulfinylation TSB Lou Phosphorus, Sulfur, and Silicon and the Related Elements 198 (6), 517-525, 2023 | 1 | 2023 |
| Scalable, Chemoselective Ni-Electrocatalytic Sulfinylation of Aryl Halides with SO2 TSB Lou, Y Kawamata, T Ewing, G Correa-Otero, M Collins, P Baran | | 2022 |