50. Catalytic Hydrodefluorination via Oxidative Addition, Ligand Metathesis, and Reductive Elimination at Bi(I)/Bi(III) Centers
Pang, Y.; Leutzsch, M.; Nöthling, N.; Katzenburg, F.; Cornella, J. J. Am. Chem. Soc. 2021, 143, 12487
49. Validation of Arylphosphorothiolates as Convergent Substrates for Ar-SF4Cl and Ar-SF5 Synthesis
Wang, L.; Ni, S.; Cornella, J. Synthesis, 2021, 53, 4308–4312
Special Issue dedicated to Prof. Sarah Reisman, recipient of the 2019 Dr. Margaret Faul Women in Chemistry Award
48. Dibismuthanes in Catalysis: from Synthesis and Characterization to Redox Behavior Towards Oxidative Cleavage of 1,2-diols
Magre, M.; Kuziola, J.; Nöthling, N.; Cornella, J. Org. Biomol. Chem. 2021, 19, 4922-4929
This article is part of the themed collections: p-Block Lewis Acids in Organic Synthesis and Catalysis & Biocatalysis in OBC
47. 16-Electron Nickel(0)-Olefin Complexes in Low-Temperature C(sp2)–C(sp3) Kumada Cross-Couplings
Lutz, S.; Nattmann, L.; Nöthling, N.; Cornella, J. Organometallics 2021, 40, 2220–2230
Special Issue: Organometallic Solutions to Challenges in Cross-Coupling
46. Catalytic Activation of N2O at a Low-Valent Bismuth Redox Platform
Pang, Y.; Leutzsch, M.; Nöthling, N.; Cornella, J. J. Am. Chem. Soc. 2020, 142, 19473.
45. Dialkyl Ether Formation at High-Valent Nickel
Le Vaillant, F.; Reijerse, E.; Leutzsch, M.; Cornella, J. J. Am. Chem. Soc. 2020, 142, 19540
44. A Unified Strategy for Arylsulfur(VI) Fluorides from Aryl Halides: Access to Ar-SOF3 Compounds
Wang, L.; Cornella, J. Angew. Chem. Int. Ed. 2020, 59, 23510-23515
Hot Paper in Angewandte Chemie International Edition.
43. Ni(4-tBu-stb)3: A Robust 16-Electron Ni(0) Olefin Complex for Catalysis
Nattmann, L.; Cornella, J. Organometallics 2020, 39, 3295
42. Bismuth-Catalyzed Oxidative Coupling of Arylboronic Acids with Triflate and Nonaflate Salts
Planas, O.; Peciukenas, V.; Cornella, J. J. Am. Chem. Soc. 2020, 142, 11382.
41. Synthesis of Sulfonyl Fluorides from Sulfonamides
Perez-Palau, M.; Cornella, J. Eur. J. Org. Chem. 2020, 2497
40. An Air-Stable Binary Ni(0)-Olefin Catalyst
Nattmann, L; Saeb, R.; Nöthling, N.; Cornella, J. Nature Catalysis 2020, 3, 6-13
39. Radical C-N Borylation of Aromatic Amines Enabled by a Pyrylium Reagent.
Ma, Y.; Pang, Y.; Chabbra, S.; Reijerse, E. J.; Schnegg, A.; Niski, J.; Leutzsch, M.; Cornella, J. Chem. -Eur. J. 2020, 26, 3738-3743.
Previously in ChemRxiv 2019, doi: 10.26434/chemrxiv.11211245.v1
38. Pyrylium Salts: Selective Reagents for the Activation of Primary Amino Groups in Organic Synthesis
Pang, Y.; Moser, D. Cornella, J. SYNTHESIS 2020, 52, 489-503.
Part of the Bürgenstock Special Edition 2019 Future Stars in Organic Chemistry
37. Facile Access to Chiral non-Natural Aminoacids
Planas, O.; Cornella, J. Nature Catalysis 2019, 2, 839. (News & Views Article)
36. Selective Late-Stage Sulfonyl Chloride Formation from Sulfonamides Enabled by Pyry-BF4
Gomez-Palomino, A.; Cornella, J. Angew. Chem. Int. Ed. 2019, 58, 18235-18239
Highlighted in Organic Process Research and Development (OPR&D) Org. Process Res. Dev. 2019, 23, 2583−2591
35. Fluorination of Arylboronic Esters Enabled by Bismuth Redox Catalysis
Planas, O.; Wang, F.; Leutszch, M.; Cornella, J. Science, 2020, 367, 313-317.
Previously in ChemRxiv (doi.org/10.26434/chemrxiv.9729143.v1)
34. Bi(I)-catalyzed Transfer-Hydrogenation with Ammonia Borane
Wang, F.; Planas, O.; Cornella, J. J. Am. Chem. Soc. 2019, 141, 4235
Highlighted in ChemBeanGo - April 2019 (available in chinese).
33. Ni-catalyzed Reductive Liebeskind-Srogl Alkylation of Heterocycles
Ma, Y.; Cammarata, J.; Cornella, J. J. Am. Chem. Soc. 2019, 141, 1918
32. A Highly Reduced Ni-Li-Olefin Complex for Kumada-Corriu Cross-Couplings
Nattmann, L.; Lutz, S.; Ortsack, P.; Goddard, R. Cornella, J. J. Am. Chem. Soc. 2018, 140, 13628