Publications

• F. Cordella, N. Dragone, R. D’Orsi, C. Saponaro, D. Vergara, M. Lessi, G. Angelici*, A Structure-Activity Relationship Study of Amino Acid Derivatives of Pterostilbene Analogues Toward Human Breast Cancer, ChemMedChem, 2024, e202300727
• G. Alonci, A. Boussard, M. Savona, F.Cordella, G. Angelici, R.Mocchi, S. Sommatis, D. Monticelli, A LC-QTOF Method for the Determination of PEGDE Residues in Dermal Fillers, Gels, 2023, 9(5), 409
• M. Pollastrini, L. Pasquinelli, M. Gorecki, F. Balzano, L. Cupellini, F. Lipparini, G. Barretta, F. Marchetti, G. Pescitelli*, G. Angelici*,, J. Org. Chem., 2022, DOI: 10.1021/acs.joc.2c01377
• G. Angelici, N. Bhattacharjee, M. Pypec, L. Jouffret, C. Didierjean, F. Jolibois, L. Perrin, O. Roy, C. Taillefumier, Org. Biom. Chem., 2022, DOI: 10.1039/D20B01351G
• M. Pierigé, A. Iuliano, G. Angelici, G. Casotti, Organics, 2022, 3(2), 87-94
• M. Pollastrini, F. Lipparini, L. Pasquinelli, F. Balzano, G. Barretta, G. Pescitelli, G. Angelici*,  J. Org. Chem., 2021, 86(12), 7946-7954
• G. Casotti, G. Fusini, M. Ferreri, L. F. Pardini, C. Evangelisti, G. Angelici*, A. Carpita, 2020, Synthesis, 52(12): 1795-1803
• G. Fusini, F. Rizzo, G. Angelici, E. Pitzalis, C. Evangelisti, A. Carpita, 2020, Catalysts, 10(3), 330
• S. Di Silvio, F. Bologna, L. Milli, D. Giuri, N. Zanna, N. Castellucci, M. Monari, M. Calvaresi, M. Górecki, G. Angelici, C. Tomasini, G. Pescitelli,  2020, Org. Biom. Chem., 865-877  
• G. Laudadio, G. Fusini, G. Casotti, C. Evangelisti, G. Angelici*, A. Carpita, J. Flow Chem., 2019, 133-143
• R. Shyam, L. Nauton, G. Angelici, O. Roy, C. Taillefumier, S. Faure, Biopolymers, 2019, 110:e23273
• R. Rossi, G. Angelici, G. Casotti, C. Manzini, M. Lessi, Catalytic synthesis of 1,2,4,5-Tetrasubstituted-1H-imidazole derivatives: State of the art, Adv. Synth. Cat., 2018, 2737-2803
• G. Angelici*, M. Gorecki, G. Pescitelli, N. Zanna, M. Monari, C. Tomasini,  Biopolymers. 2018; e23072
• G. Fusini, D. Barsanti, G. Angelici*, G. Casotti, A. Canale, G. Benelli, A. Lucchi, A. Carpita, Tetrahedron, 2018, 4381-4389
• G. Dumonteil, N. Bhattacharjee, G. Angelici, O. Roy, S. Faure, L. Jouffret, F. Jolibois, L. Perrin, C. Taillefumier, J. Org. Chem. 2018, 83, 6382−6396
• G. Angelici*, M. Gorecki, G. Pescitelli, N. Zanna, M. Monari, C. Tomasini, Synthesis and structure analysis of ferrocene-containing pseudopeptides, Biopolymers. 2017; e23072.
• G. Angelici, N. Bhattacharjee, O. Roy, S. Faure, L. Jouffret, F. Jolibois, L. Perrin, C. Didierjean, C. Taillefumier, Weak backbone CH⋯OC and side chain tBu⋯tBu London interactions help promote helix folding of achiral NtBu peptoids, Chem. Comm., 2016, 4573-4576.
•  G. Angelici*, S. Nicolet, N. R. Uda, M. Creus, Experimental and Guided Theoretical Investigation of Complex Reaction Mechanisms in a Prins Reaction of Glyoxylic Acid and Isobutylene, J. Chem. Educ., 2014, 2178–2181.
• N. R. Uda, G. Upert, G. Angelici, Stefan Nicolet, T. Schmidt, T. Schwede, M. Creus, Zinc-selective Inhibition of the Promiscuous Bacterial Amide-Hydrolase DapE: Implications of Metal Heterogeneity in Evolution and Antibiotic Drug-Design, Metallomics, 2014, 88-95.
• G. Angelici, N. Castellucci, C. Tomasini, Conformational studies on a medium size cyclopseudopeptide containing the oxazolidin-2-one moiety J. Phys. Org. Chem., 2012, 965-970.
• N. Castellucci, G. Angelici, G. Falini, M. Monari, C. Tomasini, L-Phe-D-Oxd: A Privileged Scaffold for the Formation of Supramolecular Materials, Eur. J. Org. Chem. 2011, 3082–3088.
• N. Castellucci, G. Falini, G. Angelici, C. Tomasini, Amino Acids, Formation of gels in the presence of metal ions, 2011, 609-620 C. Tomasini, G. Angelici, N. Castellucci, Foldamers Based on Oxazolidin-2-ones Eur. J. Org. Chem. 2011, 3648–3669.
• G. Angelici, N. Castellucci, G. Falini, D. Huster, M. Monari, C. Tomasini, Pseudopeptides Designed to Form Supramolecular Helixes: The Role of the Stereogenic Centers, Crystal Growth & Design, 2010, 923–929.
• G. Angelici, N. Castellucci, S. Contaldi, G. Falini, H.-J. Hofmann, M. Monari, C. Tomasini, A Network of Small Molecules Connected by Cross-Linked NH Bonds, Crystal Growth & Design, 2010, 244–251.
• M. Wiesner, G. Upert, G. Angelici, H. Wennemers, Enamine Catalysis with Low Catalyst Loadings – High Efficiency via Kinetic studies, J. Am. Chem. Soc., 2010, 6–7.
• G. Angelici, G. Falini, H. J. Hofmann, D. Huster, M. Monari, C. Tomasini, Nanofibers from Oxazolidi-2-one Containing Hybrid Foldamers: What is the Right Molecular Size?, Chem. Eur. J., 2009, 8037-8048.
• G. Angelici, R. J. Corrêa, S. J. Garden, C. Tomasini, Water influences the enantioselectivity in the proline or prolinamide-catalyzed aldol addition of acetone to isatins, Tetrahedron Letters, 2009, 814-817.
• G. Angelici, G. Falini, H. J. Hofmann, D. Huster, M. Monari, C. Tomasini, A Fiberlike Peptide Material Stabilized by Single Intermolecular Hydrogen Bonds, Angew. Chem. Int. Ed. 2008, 8075-8078.
• G. Angelici, S. Contaldi, S. L. Green, C. Tomasini, Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement, Org. Biomol. Chem., 2008, 1849-1852.
• G. Angelici, R. Tresanchez Carrera, G. Luppi, C. Tomasini, The Design and Synthesis of Dansyl-Containing Cyclic Pseudopeptides Eur. J. Org. Chem., 2008, 3552-3558.
• R. J. Correa, S. J. Garden, G. Angelici, C. Tomasini, A DFT and AIM Study of the Proline-Catalyzed Asymmetric Cross-Aldol Addition of Acetone to Isatins: A Rationalization for the Reversal of Chirality, Eur. J. Org. Chem., 2008, 736-744.
• G. Angelici, A. Falgiani, G. Luppi, B. Kaptein, Q.B. Broxterman, Atom Economic and Highly Synselective Prolinamide‐Catalyzed Cross‐aldol Addition of Hydroxyacetone to Aromatic Aldehydes, Synt. Comm, 2008, 1137-1146.
• G. Angelici, G. Luppi, B. Kaptein, Q. B. Broxterman, H. J. Hofmann, C. Tomasini, Synthesis and Secondary Structure of Alternate α,β-Hybrid Peptides Containing Oxazolidin-2-one Moieties, Eur. J. Org. Chem., 2007, 2713-2721.
• M. Lombardo, S. Licciulli, F. Pasi, G. Angelici, C. Trombini, Cobalt-Catalysed Addition of Allylidene Dipivalate to Aldehydes. A Formal Homoaldol Condensation, Advanced Synthesis & Catalysis, 2005, 2015-2018.