Publications

  • 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.