Wang, F.; Planas, O.; Cornella, J. Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane. Journal of the American Chemical Society2019, 141, 4235–4240.
Ma, Y.; Cammarata, J.; Cornella, J. Ni-Catalyzed Reductive Liebeskind–Srogl Alkylation of Heterocycles. Journal of the American Chemical Society2019, 141, 1918–1922.
O'Neill, M.; Cornella, J. Retaining Alkyl Nucleophile Regiofidelity in Transition-Metal- Mediated Cross-Couplings to Aryl Electrophiles. Synthesis2018, 50, 3974–3996.
O'Neill, M. J.; Riesebeck, T.; Cornella, J. Thorpe-Ingold Effect in Branch-Selective Alkylation of Unactivated Aryl Fluorides. Angewandte Chemie, International Edition2018, 57, 9103–9107.
Gómez‐Palomino, A.; Ghiazza, C.; Busch, J.; Wagner, L.; Cornella, J. Preparation of Pyrylium Tetrafluoroborate (Pyry-BF4); Garg, N. K., Ed.; Garg, N. K., Series ed.; Organic Syntheses: Vol. 100; John Wiley & Sons: Hoboken, 2023; Vol. 100, pp 361–381.
Wagner, L.; Ghiazza, C.; Cornella, J. Preparation of 4-(5-(p-Tolyl)-3-(Trifluoromethyl)-1H-Pyrazol-1-Yl)Benzenesulfonyl Fluoride (ArSO2F); Garg, N. K., Ed.; Garg, N. K., Series ed.; Organic Syntheses: Vol. 100; John Wiley & Sons: Hoboken, 2023; Vol. 100, pp 382–393.
Cornella, J.; Pang, Y. Organometallic Compounds of Arsenic, Antimony and Bismuth. In Comprehensive Organometallic Chemistry IV; Parkin, G., Mexer, K., O'Hare, D., Eds.; Parkin, G., Mexer, K., O'Hare, D., Series Eds.; 2022; Vol. 10, pp 478–522.
Biscoe, M. R.; Cornella, J.; Kalyani, D.; Neufeldt, S. From Established to Emerging: Evolution of Cross-Coupling Reactions. The Journal of Organic Chemistry. American Chemical Society: Washington, D.C. November 15, 2024, pp 16065–16069.
Ma, Y.; Pang, Y.; Niski, J.; Leutzsch, M.; Cornella, J. Radical C‒N Borylation of Aromatic Amines Enabled by a Pyrylium Reagent. ChemRxiv. American Chemical Society (ACS), Chinese Chemical Society, Chemical Society of Japan, German Chemical Society (GDCh), Royal Society of Chemistry December 2, 2019.
Planas, O.; Wang, F.; Leutzsch, M.; Cornella, J. Catalytic Fluorination of Boron Compounds at a Bismuth Redox Platform. ChemRxiv. American Chemical Society (ACS), Chinese Chemical Society, Chemical Society of Japan, German Chemical Society (GDCh), Royal Society of CHemistry August 26, 2019.
To be able to exploit the advantages of elements and their molecular compounds in a targeted manner, chemists have to develop a fundamental understanding of their properties. In the case of the element bismuth, a team from the Max Planck Institut für Kohlenforschung has now taken an important step.
Chemists at the institute do not always work in the lab, sometimes mainly on the computer - like Xin Gui from the Department of Molecular Theory and Spectroscopy.
The Max-Planck-Institut für Kohlenforschung is delighted about the great response to the work of its scientists - for example Prof. Frank Neese, Director of the Department of Molecular Theory and Spectroscopy.