57. Deaminative Chlorination of Aminoheterocycles
Ghiazza, C.; Faber, T.; Gómez-Palomino, A.; Cornella, J. Nat. Chem. 2022, 14, 78-84.
previously on ChemRxiv (link)
56. Bismuth Redox Catalysis: An Emerging Main-Group Platform for Organic Synthesis
55. Redox-Neutral Organometallic Elementary Steps at Bismuth: Catalytic Synthesis of Aryl Sulfonyl Fluorides
54. Tris[1,1′-[η2-(1E)-1,2-Ethenediyl]bis[4-(Trifluoromethyl)Benzene]]Nickel
Saeb, R.; Cornella, J. Encyclopedia of Reagents for Organic Synthesis, (EROS) online asap.
53. Organometallic Compounds of Arsenic, Antimony and Bismuth
52. Air-Stable tris-(stilbene)Ni(0) Complexes
51. High-valent bismuth redox catalysis
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