{"id":8,"date":"2015-04-08T11:14:00","date_gmt":"2015-04-08T09:14:00","guid":{"rendered":"http:\/\/people.unipi.it\/cloner\/?page_id=8"},"modified":"2026-08-12T18:27:04","modified_gmt":"2026-08-12T16:27:04","slug":"pubblicazioni","status":"publish","type":"page","link":"https:\/\/people.unipi.it\/gaetano_angelici\/pubblicazioni\/","title":{"rendered":"Publications"},"content":{"rendered":"<ul>\n<li>L. Dei, L. Di Nicola, L. Gherardi, F. Cordella, G. Pescitelli, G. Angelici*, Unlocking peptoid diversity through post-functionalizable chiral scaffolds, via modular, divergent and side-chain protecting-group-free synthesis, <em>Org. Biom. Chem.<\/em>, <strong>2026<\/strong>, DOI: 10.1039\/d6ob00951d<\/li>\n<li>L. Dei, S. Cadeddu, C. Taillefumier, C. Migone, A. Fabiano, A. M. Piras, M. C. Santangelo, S. Di Pietro, V. Di Bussolo, G. Angelici*, A Convenient Strategy to Access Diverse Libraries of Amphiphilic Compounds Based on Glycopeptoids, <em>Chirality<\/em>, <strong>2026<\/strong>, DOI: 10.1002\/chir.70121<\/li>\n<li>G. Casotti, G. Ciarpi, D. Rossi, B. Mennucci F. Lipparini, G.Angelici, Fotoreattore modulare e relativo metodo per eseguire una fotoreazione. <em>Brevetto italiano n. 102023000027852<\/em>, Universit\u00e0 di Pisa, (Italian Patent) deposited 22\/12\/2023 accepted 17\/03\/2026.<\/li>\n<li>G. Angelici, V. Domenici, Insegnare (e imparare) la chimica attraverso i musei e le collezioni di strumenti scientifici, <em>Chimica nella scuola<\/em>, Vol. 3 No.3, <strong>2025<\/strong>, doi.org\/10.1473\/cns.v3i3.250<\/li>\n<li>F. Cordella, G. Alonci, G. Angelici, R. Mocchi, M. Savona, G. Grimaldi, G. Galasso, S. Sommatis, C. Duce, E. Pulidori, E. Martinelli, N. Zerbinati, Effect of poly(ethylene glycol)-based cross-linker length on the physicochemical and rheological properties of hyaluronic acid hydrogels potentially applicable in the biomedical field, <em>Carbohydrate Polymer Technologies and Applications<\/em>, <strong>2025<\/strong>,11, DOI:10.1016\/j.carpta.2025.100908<\/li>\n<li>F. Cordella*, S. Faure, C. Taillefumier, G. Pescitelli, E. Martinelli, G. Alonci, Z. Liu, G. Angelici*, <em>On the Reactivity of (S)-Indoline-2-Carboxylic Acid<\/em>, Chirality, <strong>2024<\/strong>, doi.org\/10.1002\/chir.70008<\/li>\n<li>F. Cordella, N. Dragone, R. D&#8217;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, <em>ChemMedChem<\/em>, <strong>2024<\/strong>, e202300727<\/li>\n<li>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, <em>Gels<\/em>, <strong>2023<\/strong>, 9(5), 409<\/li>\n<li>M. Pollastrini, L. Pasquinelli, M. Gorecki, F. Balzano, L. Cupellini, F. Lipparini, G. Barretta, F. Marchetti, G. Pescitelli*, G. Angelici*,, <em>J. Org. Chem.<\/em>, <strong>2022<\/strong>, DOI: 10.1021\/acs.joc.2c01377<\/li>\n<li>G. Angelici, N. Bhattacharjee, M. Pypec, L. Jouffret, C. Didierjean, F. Jolibois, L. Perrin, O. Roy, C. Taillefumier, <em>Org. Biom. Chem<\/em>., <strong>2022<\/strong>, DOI: 10.1039\/D20B01351G<\/li>\n<li>M. Pierig\u00e9, A. Iuliano, G. Angelici, G. Casotti, <em>Organics<\/em>, <strong>2022<\/strong>, 3(2), 87-94<\/li>\n<li>M. Pollastrini, F. Lipparini, L. Pasquinelli, F. Balzano, G. Barretta, G. Pescitelli, G. Angelici*, \u00a0<em>J. Org. Chem.<\/em>,\u00a0<strong>2021<\/strong>, 86(12), 7946-7954<\/li>\n<li>G. Casotti, G. Fusini, M. Ferreri, L. F. Pardini, C. Evangelisti, G. Angelici*, A. Carpita, <strong>2020<\/strong>,\u00a0<em>Synthesis<\/em>, 52(12): 1795-1803<\/li>\n<li>G. Fusini, F. Rizzo, G. Angelici, E. Pitzalis, C. Evangelisti, A. Carpita, <strong>2020<\/strong>,\u00a0<em>Catalysts<\/em>, 10(3), 330<\/li>\n<li><span class=\"bold\">S. Di Silvio<\/span>,\u00a0<span class=\"bold\">F. Bologna<\/span>,\u00a0<span class=\"bold\">L. Milli<\/span>,\u00a0<span class=\"bold\">D. Giuri<\/span>,\u00a0<span class=\"bold\">N. Zanna<\/span>,\u00a0<span class=\"bold\">N. Castellucci<\/span>,\u00a0<span class=\"bold\">M. Monari<\/span>,\u00a0<span class=\"bold\">M. Calvaresi<\/span>,\u00a0<span class=\"bold\">M. G\u00f3recki<\/span>,\u00a0<span class=\"bold\">G. Angelici<\/span>,\u00a0<span class=\"bold\">C. Tomasini,<\/span><span class=\"bold\">\u00a0<\/span><span class=\"bold\">G. Pescitelli,\u00a0 <strong>2020<\/strong>,\u00a0<em>Org. Biom. Chem.<\/em>, 865-877<\/span><span class=\"bold\">\u00a0\u00a0<\/span><\/li>\n<li>G. Laudadio, G. Fusini, G. Casotti, C. Evangelisti, G. Angelici*, A. Carpita, <em>J. Flow Chem<\/em>., <strong>2019<\/strong>, 133-143<\/li>\n<li>R. Shyam, L. Nauton, G. Angelici, O. Roy, C. Taillefumier, S. Faure,\u00a0<em>Biopolymers<\/em>, <strong>2019<\/strong>, 110:e23273<\/li>\n<li>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,\u00a0<em>Adv. Synth. Cat.<\/em>,\u00a0<strong>2018<\/strong>, 2737-2803<\/li>\n<li>G. Angelici*, M. Gorecki, G. Pescitelli, N. Zanna, M. Monari, C. Tomasini,\u00a0 <em>Biopolymers<\/em>.\u00a0<strong>2018<\/strong>; e23072<\/li>\n<li>G. Fusini, D. Barsanti, G. Angelici*, G. Casotti, A. Canale, G. Benelli, A. Lucchi, A. Carpita,\u00a0<em>Tetrahedron<\/em>,\u00a0<strong>2018<\/strong>, 4381-4389<\/li>\n<li>G. Dumonteil, N. Bhattacharjee, G. Angelici, O. Roy, S. Faure, L. Jouffret, F. Jolibois, L. Perrin, C. Taillefumier, <em>J. Org. Chem.<\/em>\u00a0<strong>2018<\/strong>, 83, 6382\u22126396<\/li>\n<li>G. Angelici*, M. Gorecki, G. Pescitelli, N. Zanna, M. Monari, C. Tomasini,\u00a0Synthesis and structure analysis of ferrocene-containing pseudopeptides,\u00a0<em>Biopolymers<\/em>. <strong>2017<\/strong>; e23072.<\/li>\n<li>G. Angelici, N. Bhattacharjee, O. Roy, S. Faure, L. Jouffret, F. Jolibois, L. Perrin, C. Didierjean, C. Taillefumier, Weak backbone CH\u22efOC and side chain tBu\u22eftBu London interactions help promote helix folding of achiral NtBu peptoids, <em>Chem. Comm.<\/em>, <strong>2016<\/strong>, 4573-4576.<\/li>\n<li>\u00a0G. 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, <em>J. Chem. Educ<\/em>., <strong>2014<\/strong>, 2178\u20132181.<\/li>\n<li>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, <em>Metallomics<\/em>,<strong> 2014<\/strong>, 88-95.<\/li>\n<li>G. Angelici, N. Castellucci, C. Tomasini, Conformational studies on a medium size cyclopseudopeptide containing the oxazolidin-2-one moiety <em>J. Phys. Org. Chem<\/em>., <strong>2012<\/strong>, 965-970.<\/li>\n<li>N. Castellucci, G. Angelici, G. Falini, M. Monari, C. Tomasini, L-Phe-D-Oxd: A Privileged Scaffold for the Formation of Supramolecular Materials, <em>Eur. J. Org. Chem<\/em>. <strong>2011<\/strong>, 3082\u20133088.<\/li>\n<li>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. <em>J. Org. Chem<\/em>. <strong>2011<\/strong>, 3648\u20133669.<\/li>\n<li>G. Angelici, N. Castellucci, G. Falini, D. Huster, M. Monari, C. Tomasini, Pseudopeptides Designed to Form Supramolecular Helixes: The Role of the Stereogenic Centers, <em>Crystal Growth &amp; Design<\/em>, <strong>2010<\/strong>, 923\u2013929.<\/li>\n<li>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, <em>Crystal Growth &amp; Design<\/em>, <strong>2010<\/strong>, 244\u2013251.<\/li>\n<li>M. Wiesner, G. Upert, G. Angelici, H. Wennemers, Enamine Catalysis with Low Catalyst Loadings &#8211; High Efficiency via Kinetic studies, <em>J. Am. Chem. Soc.<\/em>, <strong>2010<\/strong>, 6\u20137.<\/li>\n<li>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?, <em>Chem. Eur. J.<\/em>, <strong>2009<\/strong>, 8037-8048.<\/li>\n<li>G. Angelici, R. J. Corr\u00eaa, S. J. Garden, C. Tomasini, Water influences the enantioselectivity in the proline or prolinamide-catalyzed aldol addition of acetone to isatins, <em>Tetrahedron Letters<\/em>, <strong>2009<\/strong>, 814-817.<\/li>\n<li>G. Angelici, G. Falini, H. J. Hofmann, D. Huster, M. Monari, C. Tomasini, A Fiberlike Peptide Material Stabilized by Single Intermolecular Hydrogen Bonds, <em>Angew. Chem. Int. Ed<\/em>. <strong>2008<\/strong>, 8075-8078.<\/li>\n<li>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, <em>Org. Biomol. Chem<\/em>., <strong>2008<\/strong>, 1849-1852.<\/li>\n<li>G. Angelici, R. Tresanchez Carrera, G. Luppi, C. Tomasini, The Design and Synthesis of Dansyl-Containing Cyclic Pseudopeptides <em>Eur. J. Org. Chem<\/em>., <strong>2008<\/strong>, 3552-3558.<\/li>\n<li>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, <em>Eur. J. Org. Chem<\/em>., <strong>2008<\/strong>, 736-744.<\/li>\n<li>G. Angelici, A. Falgiani, G. Luppi, B. Kaptein, Q.B. Broxterman, Atom Economic and Highly Synselective Prolinamide\u2010Catalyzed Cross\u2010aldol Addition of Hydroxyacetone to Aromatic Aldehydes, <em>Synt. Comm<\/em>, <strong>2008<\/strong>, 1137-1146.<\/li>\n<li>G. Angelici, G. Luppi, B. Kaptein, Q. B. Broxterman, H. J. Hofmann, C. Tomasini, Synthesis and Secondary Structure of Alternate \u03b1,\u03b2-Hybrid Peptides Containing Oxazolidin-2-one Moieties, <em>Eur. J. Org. Chem.<\/em>, <strong>2007<\/strong>, 2713-2721.<\/li>\n<li>M. Lombardo, S. Licciulli, F. Pasi, G. Angelici, C. Trombini, Cobalt-Catalysed Addition of Allylidene Dipivalate to Aldehydes. A Formal Homoaldol Condensation, <em>Advanced Synthesis &amp; Catalysis<\/em>, <strong>2005<\/strong>, 2015-2018.<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>L. Dei, L. Di Nicola, L. Gherardi, F. Cordella, G. Pescitelli, G. Angelici*, Unlocking peptoid diversity through post-functionalizable chiral scaffolds,&hellip;<\/p>\n<p><a class=\"btn btn-dark btn-sm unipi-read-more-link\" href=\"https:\/\/people.unipi.it\/gaetano_angelici\/pubblicazioni\/\">Leggi tutto&#8230;<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-8","page","type-page","status-publish","hentry"],"acf":[],"featured_image_src":null,"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Publications - Gaetano Angelici<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/people.unipi.it\/gaetano_angelici\/pubblicazioni\/\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Publications - Gaetano Angelici\" \/>\n<meta property=\"og:description\" content=\"L. 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