Publications

F. Cordella*, S. Faure, C. Taillefumier, G. Pescitelli, E. Martinelli, G. Alonci, Z. Liu, G. Angelici*, On the Reactivity of (S)-Indoline-2-Carboxylic Acid, Chirality, 2024, doi.org/10.1002/chir.70008
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^*, A unique and stable Polyproline I helix sorted out from conformational equilibrium by solvent polarity, J. Org. Chem., 2022, 87, 21, 13715–13725
G. Angelici, N. Bhattacharjee, M. Pypec, L. Jouffret, C. Didierjean, F. Jolibois, L. Perrin, O. Roy, C. Taillefumier, Unveiling the conformational landscape of achiral all-cis tert-Butyl b-peptoids, Org. Biom. Chem., 2022, 20, 7907-7915
M. Pierigé, A. Iuliano, G. Angelici, G. Casotti, Stabilized Arylzinc Iodides in Negishi Acylative Cross-Coupling: A Modular Synthesis of Chalcones, Organics, 2022, 3(2), 87-94
M. Pollastrini, F. Lipparini, L. Pasquinelli, F. Balzano, G. Barretta, G. Pescitelli, G. Angelici*, A Proline Mimetic for the Design of New Stable Secondary Structures: Solvent-Dependent Amide Bond Isomerization of (S)-Indoline-2-carboxylic Acid Derivatives, J. Org. Chem., 2021, 86(12), 7946-7954
G. Casotti, G. Fusini, M. Ferreri, L. F. Pardini, C. Evangelisti, G. Angelici*, A. Carpita, Total Synthesis of Asparenydiol by Two Sonogashira Cross-Coupling Reactions Promoted by Supported Pd and Cu Catalysts, 2020, Synthesis, 52(12): 1795-1803
G. Fusini, F. Rizzo, G. Angelici, E. Pitzalis, C. Evangelisti, A. Carpita, Polyvinylpyridine-Supported Palladium Nanoparticles: An Efficient Catalyst for Suzuki–Miyaura Coupling Reactions, 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, Elusive p-helical peptide foldamers spotted by chiroptical studies, 2020, Org. Biom. Chem., 865-877
G. Laudadio, G. Fusini, G. Casotti, C. Evangelisti, G. Angelici*, A. Carpita, Synthesis of Pterostilbene through supported-catalyst promoted Mizoroki-Heck reaction, and its transposition in continuous flow reactor, 2019, J. Flow Chem., 133-143
R. Shyam, L. Nauton, G. Angelici, O. Roy, C. Taillefumier, S. Faure, NCα-gem-dimethylated peptoid side chains: A novel approachfor structural control and peptide sequence mimetics, 2019, Biopolymers, 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, Synthesis and structure analysis of ferrocene-containing pseudopeptides, Biopolymers. 2018; e23072
G. Fusini, D. Barsanti, G. Angelici*, G. Casotti, A. Canale, G. Benelli, A. Lucchi, A. Carpita, Identification and synthesis of new sex-specificcomponents of olive fruit fly (Bactrocera Oleae) female rectal gland, through original Negishi reactions on supported catalysts, Tetrahedron, 2018, 4381-4389
G. Dumonteil, N. Bhattacharjee, G. Angelici, O. Roy, S. Faure, L. Jouffret, F. Jolibois, L. Perrin, C. Taillefumier, Exploring the Conformation of Mixed Cis−Trans α,β-Oligopeptoids: A Joint Experimental and Computational Study, J. Org. Chem. 2018, 83, 6382−6396
L. Arrico, G. Angelici, L. Di Bari, Taking advantage of Co(II) induced enhanced VCD for the fast and sensitive determination of enantiomeric excess, Org. Biomol. Chem., 2017, 15, 9800–9803.
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, Formation of gels in the presence of metal ions, Amino Acids, 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.