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
30. Retaining Alkyl Nucleophile Regiofidelity in Transition-Metal-Mediated Cross-Couplings to Aryl Electrophiles
O'Neill, M. J.; Cornella, J. SYNTHESIS, 2018, 50, 3974.
29. Selective Functionalization of Aminoheterocycles by a Pyrylium Salt
Moser, D.;* Duan, Y.;* Wang, F.; Ma, Y.; O'Neill, M. J.; Cornella, J. Angew. Chem. Int. Ed. 2018, 57, 11035.
Highlighted in SynFacts, 2018, 14, 1123
28. Thorpe-Ingold Effect for Branch-Selective Alkylation of Unactivated Aryl Fluorides
O’Neill, M. J.;* Riesebeck, T.;* Cornella, J. Angew. Chem. Int. Ed. 2018, 57, 9103 (* equal contribution)
Highlighted in SynFacts, 2018, 14, 967
Prior to MPI
27. CITU: A Peptide and Decarboxylative Coupling Reagent.
Justine N. deGruyter, Lara R. Malins, Laurin Wimmer, Khalyd J. Clay, Javier Lopez-Ogalla, Tian Qin, Josep Cornella, Zhiqing Liu, Guanda Che, Denghui Bao, Jason M. Stevens, Jennifer X. Qiao, Martin P. Allen, Michael A. Poss, and Phil S. Baran. Org. Lett. 2017, 19, 6196.
26. Remote Carboxylation of Halogenated Aliphatic Hydrocarbons with Carbon Dioxide
Juliá-Hernandez, F.; Moragas, T.; Cornella, J; Martin, R. Nature, 2017, 545, 84.
25. Alkyl-(Hetero)Aryl Bond Formation via Decarboxylative Cross-Coupling: A Systematic Analysis.
Sandfort, F.;* O’Neill, M. J.;* Cornella, J.; Wimmer, L.; Baran, P. S. Angew. Chem. Int. Ed. 2017, 56, 3319.