Magre, M.; Cornella, J. Redox-Neutral Organometallic Elementary Steps at Bismuth: Catalytic Synthesis of Aryl Sulfonyl Fluorides. Journal of the American Chemical Society2021, 143, 21497–21502.
Wang, L.; Ni, S.; Cornella, J. Validation of Arylphosphorothiolates as Convergent Substrates for Ar-SF4Cl and Ar-SF5 Synthesis. Synthesis2021, 53, 4308–4312.
Pang, Y.; Leutzsch, M.; Nöthling, N.; Katzenburg, F.; Cornella, J. Catalytic Hydrodefluorination via Oxidative Addition, Ligand Metathesis, and Reductive Elimination at Bi(I)/Bi(III) Centers. Journal of the American Chemical Society2021, 143, 12487–12493.
Magre, M.; Kuziola, J.; Nöthling, N.; Cornella, J. Dibismuthanes in catalysis: from synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols. Organic & Biomolecular Chemistry2021, 19, 4922–4929.
Wang, L.; Cornella, J. A Unified Strategy for Arylsulfur(VI) Fluorides from Aryl Halides: Access to Ar‐SOF3 Compounds. Angewandte Chemie International Edition2020, 59, 23510–23515.
Le Vaillant, F.; Reijerse, E. J.; Leutzsch, M.; Cornella, J. Dialkyl Ether Formation at High-Valent Nickel. Journal of the American Chemical Society2020, 142, 19540–19550.
Pang, Y.; Leutzsch, M.; Nöthling, N.; Cornella, J. Catalytic Activation of N2O at a Low-Valent Bismuth Redox Platform. Journal of the American Chemical Society2020, 142, 19473–19479.
Planas, O.; Peciukenas, V.; Cornella, J. Bismuth-Catalyzed Oxidative Coupling of Arylboronic Acids with Triflate and Nonaflate Salts. Journal of the American Chemical Society2020, 142, 11382–11387.
Ma, Y.; Pang, Y.; Chabbra, S.; Reijerse, E. J.; Schnegg, A.; Niski, J.; Leutzsch, M.; Cornella, J. Radical C−N Borylation of Aromatic Amines Enabled by a Pyrylium Reagent. Chemistry – A European Journal2020, 26, 3738–3743.
Pang, Y.; Moser, D.; Cornella, J. Pyrylium Salts: Selective Reagents for the Activation of Primary Amino Groups in Organic Synthesis. Synthesis2020, 52, 489–503.
Gómez‐Palomino, A.; Cornella, J. Selective Late‐Stage Sulfonyl Chloride Formation from Sulfonamides Enabled by Pyry‐BF4. Angewandte Chemie, International Edition2019, 58, 18235–18239.