[18]     “Replacing the BO in BODIPY: unlocking the path to SBDIPY and BIDIPY chromophores” 

            A. Korzun, S. Crespi, C. Golz, A. Bismuto, Chem. Sci. 2023, 14, 6579

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[17]     “Mechanistically informed selection rules for competing β-hydride and β-heteroatom eliminations” 

            M. K. Bogdos, O. Stepanović, A. Bismuto, M. G. Luraschi, B. Morandi, Nature Synthesis 2022, 1, 787

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[16]     “One to find them all: a general route to Ni(I) phenolate species” 

            A. Bismuto, P. Müller, P. Finkelstein N. Trapp, J. Gunnar, B. Morandi, J. Am. Chem. Soc. 2021, 143, 10642

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[15]      “Ruthenium‐Catalyzed Dehydrogenation Through an Intermolecular Hydrogen Atom Transfer Mechanism”

             L. Huang, A. Bismuto, S. A. Rath, N. Trapp, B. Morandi, Angew. Chem. Int. Ed. 2021, 60, 7290

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[14]      “Palladium-catalyzed Chlorocarbonylation of Aryl (Pseudo) Halides Through in situ Generation of Carbon Monoxide”

             P. Boehm, S. Roediger, A. Bismuto, B. Morandi, Angew. Chem. Int. Ed. 2020, 132, 18043

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[13]      “Nickel-catalyzed Amination of Aryl Thioethers: A Combined Synthetic and Mechanistic Study”

            A. Bismuto, T. Delcaillau, P. Müller, B. Morandi, ACS Catalysis 2020, 10, 4630

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[12]      “Iridium-Catalyzed Hydrochlorination and Hydrobromination of Alkynes by Shuttle Catalysis”

              P. Yu, A. Bismuto, B. Morandi, Angew. Chem. Int. Ed. 2020, 59, 2904 

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[11]      “Nickel-Catalyzed Inter- and Intramolecular Aryl Thioether Metathesis by Reversible Arylation”

             T. Delcaillau, A. Bismuto, Z. Lian, B. Morandi, Angew. Chem. Int. Ed. 2020, 59, 2110 

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[10]      “Origin of the Difference in Reactivity between Ir Catalysts for the Borylation of C–H Bonds” 

              R. J. Oeschger, M. A. Larsen, A. Bismuto, J. F. Hartwig, J. Am. Chem. Soc. 2019, 41, 16479

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[9]        “Zwitterion-initiated hydroboration of alkynes and styrenes”

              A. Bismuto*,  M. J. Cowley, S. P. Thomas, Adv. Synth.Catal. 2021, 363, 2382

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[8]       “Characterization of the zwitterionic intermediate in 1,1-carboboration of alkynes”

             A. Bismuto, G. S. Nichol, F. D. Gonzalez, M. J. Cowley, S. P. Thomas, Angew. Chem. Int. Ed. 2020, 59, 12731

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[7]       “Silyl Anion Initiated Hydroboration of Aldehydes and Ketones”

             M. W. Stanford, A. Bismuto,  M. J. Cowley, Chem. Eur J. 2020, 26, 9855

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[6]       “Aluminum-catalyzed hydroboration of alkenes”

             A. Bismuto, M. J. Cowley, S. P. Thomas, ACS Catalysis 2018, 8, 2001

 

[5]       “Borane-catalyzed hydroboration of alkynes and alkenes”

             N. W. J. Ang, C. S. Buettner, S. Docherty, A. Bismuto, J. R. Carney, J. H. Docherty, M. J. Cowley, S. P. Thomas, Synthesis 2017, 50, 803

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[4]       “Aluminum hydride catalyzed hydroboration of alkynes”

             A. Bismuto, S. P. Thomas, M. J. Cowley, Angew. Chem. Int. Ed. 2016, 55, 15356 

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[3]       “Catalytic α-arylation of imines leading to N-unprotected indoles and azaindoles”

             E. Marelli, M. Corpet, Y. Minenkov, R. M. Neyyappadath, A. Bismuto, G. Buccolini, M. Curcio, L. Cavallo, S. P. Nolan, ACS Catalysis 2016, 6, 2930

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[2]       “Mild, Selective and Efficient Oxidation of Sulfides to Sulfoxides Catalyzed by Mn (III)-Salen Complexes”

            A. Bismuto, M. E. Cucciolito, F. Ruffo, A. Vitagliano, M. Curcio, Phosphorus, Sulfur, and Silicon and the Related Elements 2015, 190, 1021 

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[1]       “The elpaN-salen series: multifunctional ligands based on D-glucose for the Mn(III)-catalyzed enantioselective epoxidation of styrenes”

             F. Ruffo, A. Bismuto, A. Carpentieri, M. E. Cucciolito, M. Lega, Inorg. Chim. Acta 2013, 405, 288