Antonio Mezzetti

Affiliations: 
Eidgenössische Technische Hochschule Zürich, Zürich, ZH, Switzerland 
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"Antonio Mezzetti"
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Passera A, Mezzetti A. (2021) Retraction: The Manganese(I)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones: Disclosing the Macrocylic Privilege. Angewandte Chemie (International Ed. in English). 59: 14722
Luca L, Mezzetti A. (2020) Chiral Benzoins via Asymmetric Transfer Hemihydrogenation of Benzils: The Detail that Matters. The Journal of Organic Chemistry
Passera A, Mezzetti A. (2019) The Manganese(I)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones: Disclosing the Macrocylic Privilege. Angewandte Chemie (International Ed. in English). 59: 187-191
De Luca L, Passera A, Mezzetti A. (2019) Asymmetric Transfer Hydrogenation with a Bifunctional Iron(II) Hydride: Experiment Meets Computation. Journal of the American Chemical Society
Schotes C, Mezzetti A. (2019) Enantioselective Diels-Alder Reactions of Unsaturated β-Ketoesters Catalyzed by Chiral Ruthenium PNNP Complexes. Chimia. 65: 231-234
De Luca L, Mezzetti A. (2018) Base-free Asymmetric Transfer Hydrogenation of 1,2-Di- and Monoketones Catalyzed by a Chiral Iron(II) Hydride. Chimia. 72: 233-237
Bigler R, Huber R, Mezzetti A. (2015) Highly enantioselective transfer hydrogenation of ketones with chiral (NH)2 P2 macrocyclic iron(II) complexes. Angewandte Chemie (International Ed. in English). 54: 5171-4
Bigler R, Mezzetti A. (2014) Isonitrile iron(II) complexes with chiral N2P2 macrocycles in the enantioselective transfer hydrogenation of ketones. Organic Letters. 16: 6460-3
Patchett R, Magpantay I, Saudan L, et al. (2013) Asymmetric hydrogenation of ketones with H2 and ruthenium catalysts containing chiral tetradentate S2N2 ligands. Angewandte Chemie (International Ed. in English). 52: 10352-5
Schotes C, Althaus M, Aardoom R, et al. (2012) Asymmetric Diels-Alder and Ficini reactions with alkylidene β-ketoesters catalyzed by chiral ruthenium PNNP complexes: mechanistic insight. Journal of the American Chemical Society. 134: 1331-43
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