General Description Group Composition Contacts Recent Publications News Collaborations How to join us

General Description

Why "Bioorganic Chemistry"? It is because the main scientific interest of the group, that is organic synthesis, has always been intertwined with biological applications and biological means. Thus the group has synthesized biologically active molecules since 1983 (among them particularly noteworthy are beta-lactam antibiotics and enediynes) and has used biological tools (enzymes-microorganisms) for organic synthesis since 1985. The group is strongly active also in the synthesis of Active Pharmaceutical Ingredients. In the last 20 years the group has been deeply involved in diversity-oriented synthesis of drug-like molecules (in particular novel heterocycles). Towards that goal we have thoroughly used multicomponent reactions (but also solid-phase combinatorial synthesis and flow chemistry). Recently, the group is becoming more and more interested in the chemical contribution to Bioeconomy.

During the last 17 years, the group has been mainly active in Diversity Oriented Synthesis of libraries of drug-like molecules, especially using Multicomponent reactions (MCRs). They are, for their intimate nature, extremely convergent, producing a remarkably high increase of molecular complexity in just one step. Therefore, especially when the components may be varied at will, they are very well suited for the generation of libraries. Among MCRs, those based on the peculiar reactivity of isocyanides, such as the Ugi and the Passerini reactions or their modifications, have been among the most widely used, also in an industrial context.

Apart from that, the group has a 360° experience in organic synthesis (e.g. stereoselective synthesis, organocatalysis, biocatalysis, heterocycle synthesis and so on). Due to this well reknown experience in synthetic chemistry the BOG group is also involved in custom organic synthesis both of libraries and of APIs. We have always collaborated with private companies and are always happy to share our expertise with the industrial world.

Recently the group is also active in new fields. In particular flow chemistry and photoactivated reactions. You can see a video on photoredox reactons here:

Contrary to what typically happens elsewhere, our group is formed by more than one professor. This is because we strongly believe that joining our efforts will allow to reach a sufficient critical mass. Thus, while each professor has his/her own independent research programmes, we share facilities, reagents, instruments, intermediates and discuss weekly in our group meetings the results of our research. In this way, our students can come in contact with several research projects, learning much more than what directly regards their own programme.

Finally, our group is strongly committed to internationalization, and several of our students (both at master and Ph.D. level) carry out their theses through secondment periods in other european countries.

Group Composition

Surname Name Role CV (or link to CV) Picture
BANFI Luca Full Professor
RIVA Renata Associate Professor
BASSO Andrea Associate Professor
MONI Lisa Tenure-track Assistant Professor
LAMBRUSCHINI Chiara Post-doctoral Fellow go to CV
ANSELMO Manuel Ph. D. student go to CV
VITALI FORCONESI Gabriella Ph. D. student go to CV
NOLA Marta master student go to CV
LESS Giulio master student go to CV
PUSCEDDU Gianluca master student go to CV
FERRARO Francesco master student go to CV
CAPURRO Pietro master student go to CV
CARTAGENOVA Daniele master student go to CV
SPEICH Elena master student go to CV
GRIVA Sirio master student go to CV
CHERUBIN Alberto master student go to CV
BARUZZO Giulia master student go to CV
DI STEFANO Daniele master student go to CV
GUGLIOTTA Davide master student go to CV
ISMAIL Hossny master student go to CV


Contact Luca Banfi: E-mail:

Recent publications

  1. Anselmo, M., Moni, L., Ismail, H., Comoretto, D., Riva, R. and Basso, A., Photocatalyzed synthesis of isochromanones and isobenzofuranones under batch and flow conditions, Beilstein Journal of Organic Chemistry 2017, 13, 1456-1462.
  2. Giustiniano, M.; Basso, A.; Mercalli, V.; Massarotti, A.; Novellino, E.; Tron, G. C.; Zhu, J. P., To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis, Chemical Society Reviews, 2017, 46, 1295-1357.
  3. Banfi, L.; Basso, A.; Lambruschini, C.; Moni, L.; Riva, R., Synthesis of Seven-membered Nitrogen Heterocycles through the Ugi Multicomponent Reaction, Chemistry of Heterocyclic Compounds, 2017, 53, 382.
  4. Virgone-Carlotta, A.; Dufour, E.; Bacot, S.; Ahmadi, M.; Cornou, M.; Moni, L.; Garcia, J.; Chierici, S.; Garin, D.; Marti-Batlle, D.; Perret, P.; Ghersi-Egea, J. F.; Sallanon, M. M.; Fagret, D.; Ghezzi, C., New diketopiperazines as vectors for peptide protection and brain delivery: Synthesis and biological evaluation, Journal of Labelled Compounds & Radiopharmaceuticals, 2016, 59, 517-530.
  5. Veronesi, M.; Giacomina, F.; Romeo, E.; Castellani, B.; Ottonello, G.; Lambruschini, C.; Garau, G.; Scarpelli, R.; Bandiera, T.; Piomelli, D.; Dalvit, C., Fluorine nuclear magnetic resonance-based assay in living mammalian cells, Analytical Biochemistry, 2016, 495, 52-59.
  6. Spallarossa, M.; Banfi, L.; Basso, A.; Moni, L.; Riva, R., Access to Polycyclic Alkaloid-Like Structures by Coupling the Passerini and Ugi Reactions with Two Sequential Metal-Catalyzed Cyclizations, Advanced Synthesis & Catalysis, 2016, 358, 2940-2948.
  7. Moni, L.; Gers-Panther, C. F.; Anselmo, M.; Muller, T. J. J.; Riva, R., Highly Convergent Synthesis of Intensively Blue Emissive Furo 2,3-c isoquinolines by a Palladium-Catalyzed Cyclization Cascade of Unsaturated Ugi Products, Chemistry-a European Journal, 2016, 22, 2020-2031.
  8. Spallarossa, M.; Wang, Q.; Riva, R.; Zhu, J. P., Synthesis of Vinyl Isocyanides and Development of a Convertible Isonitrile, Organic Letters, 2016, 18, 1622-1625.
  9. Moni, L.; Banfi, L.; Riva, R.; Basso, A., External-Oxidant-Based Multicomponent Reactions, Synthesis-Stuttgart, 2016, 48, 4050-4059.
  10. Moni, L.; Banfi, L.; Basso, A.; Martino, E.; Riva, R., Diastereoselective Passerini Reaction of Biobased Chiral Aldehydes: Divergent Synthesis of Various Polyfunctionalized Heterocycles, Organic Letters, 2016, 18, 1638-1641. Errata corrige: p. 3306.
  11. Moni, L.; Banfi, L.; Basso, A.; Bozzano, A.; Spallarossa, M.; Wessjohann, L.; Riva, R., Passerini Reactions on Biocatalytically Derived Chiral Azetidines, Molecules, 2016, 21.
  12. Lambruschini, C.; Banfi, L.; Guanti, G., Switching the Photochromic Activity of Acenaphthylene Derivatives through a Tandem Nucleophile-Promoted Addition Reaction, Chemistry-a European Journal, 2016, 22, 13831-13834.
  13. Garbarino, S.; Ravelli, D.; Protti, S.; Basso, A., Photoinduced Multicomponent Reactions, Angewandte Chemie-International Edition, 2016, 55, 15476-15484.
  14. Cini, E.; Banfi, L.; Barreca, G.; Carcone, L.; Malpezzi, L.; Manetti, F.; Marras, G.; Rasparini, M.; Riva, R.; Roseblade, S.; Russo, A.; Taddei, M.; Vitale, R.; Zanotti-Gerosa, A., Convergent Synthesis of the Renin Inhibitor Aliskiren Based on C5-C6 Disconnection and CO2H-NH2 Equivalence, Organic Process Research & Development, 2016, 20, 270-283.
  15. Caputo, S.; Basso, A.; Moni, L.; Riva, R.; Rocca, V.; Banfi, L., Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction, Beilstein Journal of Organic Chemistry, 2016, 12, 139-143.
  16. Tassano, E.; Alama, A.; Basso, A.; Dondo, G.; Galatini, A.; Riva, R.; Banfi, L., Conjugation of Hydroxytyrosol with Other Natural Phenolic Fragments: From Waste to Antioxidants and Antitumour Compounds, European Journal of Organic Chemistry, 2015, 6710-6726.
  17. Moni, L.; Denissen, M.; Valentini, G.; Muller, T. J. J.; Riva, R., Diversity-Oriented Synthesis of Intensively Blue Emissive 3-Hydroxyisoquinolines by Sequential Ugi Four-Component Reaction/Reductive Heck Cyclization, Chemistry-a European Journal, 2015, 21, 753-762.
  18. Moni, L.; Banfi, L.; Basso, A.; Carcone, L.; Rasparini, M.; Riva, R., Ugi and Passerini Reactions of Biocatalytically Derived Chiral Aldehydes: Application to the Synthesis of Bicyclic Pyrrolidines and of Antiviral Agent Telaprevir, Journal of Organic Chemistry, 2015, 80, 3411-3428.
  19. Gardella, L.; Basso, A.; Prato, M.; Monticelli, O., On stereocomplexed polylactide materials as support for PAMAM dendrimers: synthesis and properties, Rsc Advances, 2015, 5, 46774-46784.
  20. Garbarino, S.; Protti, S.; Basso, A., Toward a Green Atom Economy: Development of a Sustainable Multicomponent Reaction, Synthesis-Stuttgart, 2015, 47, 2385-2390.
  21. Terol, A.; Ardini, F.; Basso, A.; Grotti, M., Determination of selenium urinary metabolites by high temperature liquid chromatography-inductively coupled plasma mass spectrometry, Journal of Chromatography A, 2015, 1380, 112-119.
  22. Veronesi, M.; Romeo, E.; Lambruschini, C.; Piomelli, D.; Bandiera, T.; Scarpelli, R.; Garau, G.; Dalvit, C., Fluorine NMR-Based Screening on Cell Membrane Extracts, Chemmedchem, 2014, 9, 286-289.
  23. Monticelli, O.; Putti, M.; Gardella, L.; Cavallo, D.; Basso, A.; Prato, M.; Nitti, S., New Stereocomplex PLA-Based Fibers: Effect of POSS on Polymer Functionalization and Properties, Macromolecules, 2014, 47, 4718-4727.
  24. Moni, L.; Banfi, L.; Basso, A.; Galatini, A.; Spallarossa, M.; Riva, R., Enantio- and Diastereoselective Synthesis of Highly Substituted Benzazepines by a Multicomponent Strategy Coupled with Organocatalytic and Enzymatic Procedures, Journal of Organic Chemistry, 2014, 79, 339-351.
  25. Moni, L.; Banfi, L.; Basso, A.; Brambilla, A.; Riva, R., Diversity-oriented synthesis of dihydrobenz-oxazepinones by coupling the Ugi multicomponent reaction with a Mitsunobu cyclization, Beilstein Journal of Organic Chemistry, 2014, 10, 209-212.
  26. Garbarino, S.; Banfi, L.; Riva, R.; Basso, A., Three in the Spotlight: Photoinduced Stereoselective Synthesis of (Z)-Acyloxyacrylamides through a Multicomponent Approach, Journal of Organic Chemistry, 2014, 79, 3615-3622.
  27. Dufour, E.; Moni, L.; Bonnat, L.; Chierici, S.; Garcia, J., 'Clickable' 2,5-diketopiperazines as scaffolds for ligation of biomolecules: their use in A beta inhibitor assembly, Organic & Biomolecular Chemistry, 2014, 12, 4964-4974.
  28. De Moliner, F.; Bigatti, M.; De Rosa, C.; Banfi, L.; Riva, R.; Basso, A., Synthesis of triazolo-fused benzoxazepines and benzoxazepinones via Passerini reactions followed by 1,3-dipolar cycloadditions, Molecular Diversity, 2014, 18, 473-482.
  29. De Moliner, F.; Bigatti, M.; Banfi, L.; Riva, R.; Basso, A., OPHA (Oxidation-Passerini-Hydrolysis-Alkylation) Strategy: a Four-Step, One-Pot Improvement of the Alkylative Passerini Reaction, Organic Letters, 2014, 16, 2280-2283.
  30. Banfi, L.; Basso, A.; Moni, L.; Riva, R., The Alternative Route to Enantiopure Multicomponent Reaction Products: Biocatalytic or Organocatalytic Enantioselective Production of Inputs for Multicomponent Reactions, European Journal of Organic Chemistry, 2014, 2014, 2005-2015.
  31. Morana, F.; Basso, A.; Riva, R.; Rocca, V.; Banfi, L., The homo-PADAM Protocol: Stereoselective and Operationally Simple Synthesis of alpha-Oxo- or alpha-Hydroxy-gamma-acylaminoamides and Chromanes, Chemistry-a European Journal, 2013, 19, 4563-4569.
  32. Moni, L.; Marra, A.; Skotnicki, J. S.; Koehn, F. E.; Abou-Gharbia, M.; Dondoni, A., Synthesis of rapamycin glycoconjugates via a CuAAC-based approach, Tetrahedron Letters, 2013, 54, 6999-7003.
  33. Lambruschini, C.; Veronesi, M.; Romeo, E.; Garau, G.; Bandiera, T.; Piomelli, D.; Scarpelli, R.; Dalvit, C., Development of Fragment-Based n-FABS NMR Screening Applied to the Membrane Enzyme FAAH, Chembiochem, 2013, 14, 1611-1619.
  34. Gardella, L.; Basso, A.; Prato, M.; Monticelli, O., PLA/POSS Nanofibers: A Novel System for the Immobilization of Metal Nanoparticles, Acs Applied Materials & Interfaces, 2013, 5, 7688-7692.
  35. Bertolacci, L.; Romeo, E.; Veronesi, M.; Magotti, P.; Albani, C.; Dionisi, M.; Lambruschini, C.; Scarpelli, R.; Cavalli, A.; De Vivo, M.; Piomelli, D.; Garau, G., A Binding Site for Nonsteroidal Anti-inflammatory Drugs in Fatty Acid Amide Hydrolase, Journal of the American Chemical Society, 2013, 135, 22-25.
  36. Basso, A.; Banfi, L.; Garbarino, S.; Riva, R., Ketene Three-Component Reaction: A Metal-Free Multicomponent Approach to Stereodefined Captodative Olefins, Angewandte Chemie-International Edition, 2013, 52, 2096-2099.
  37. Banfi, L.; Bagno, A.; Basso, A.; De Santis, C.; Riva, R.; Rastrelli, F., Long-Range Diastereoselectivity in an Ugi Reaction: Stereocontrolled and Diversity-Oriented Synthesis of Tetrahydrobenzoxazepines, European Journal of Organic Chemistry, 2013, 2013, 5064-5075.
  38. Sonaglia, L.; Banfi, L.; Riva, R.; Basso, A., Multicomponent approach to the alkaloid-type 2-aza-7-oxabicyclo 4.3.0 nonane framework, Tetrahedron Letters, 2012, 53, 6516-6518.
  39. Morana, F.; Basso, A.; Bella, M.; Riva, R.; Banfi, L., Organocatalytic Asymmetric Synthesis of beta-Aryl-beta-isocyano Esters, Advanced Synthesis & Catalysis, 2012, 354, 2199-2210.
  40. Cerulli, V.; Banfi, L.; Basso, A.; Rocca, V.; Riva, R., Diversity oriented and chemoenzymatic synthesis of densely functionalized pyrrolidines through a highly diastereoselective Ugi multicomponent reaction, Organic & Biomolecular Chemistry, 2012, 10, 1255-1274.
  41. Bisignano, P.; Lambruschini, C.; Bicego, M.; Murino, V.; Favia, A. D.; Cavalli, A., In Silico Deconstruction of ATP-Competitive Inhibitors of Glycogen Synthase Kinase-3 beta, Journal of Chemical Information and Modeling, 2012, 52, 3233-3244.
  42. Banfi, L.; Basso, A.; Chiappe, C.; De Moliner, F.; Riva, R.; Sonaglia, L., Development of a stereoselective Ugi reaction starting from an oxanorbornene beta-amino acid derivative, Organic & Biomolecular Chemistry, 2012, 10, 3819-3829.
  43. Riva, R.; Banfi, L.; Castaldi, G.; Ghislieri, D.; Malpezzi, L.; Musumeci, F.; Tufaro, R.; Rasparini, M., Selective Chemical Oxidation of Risperidone: A Straightforward and Cost-Effective Synthesis of Paliperidone, European Journal of Organic Chemistry, 2011, 2319-2325.
  44. Riva, R.; Banfi, L.; Basso, A.; Zito, P., A new diversity oriented and metal-free approach to highly functionalized 3H-pyrimidin-4-ones, Organic & Biomolecular Chemistry, 2011, 9, 2107-2122.
  45. De Moliner, F.; Crosignani, S.; Galatini, A.; Riva, R.; Basso, A., Novel Application of alpha-Azido Aldehydes in Multicomponent Reactions: Synthesis of Triazolo-Fused Dihydrooxazinones via a Passerini Reaction-Dipolar Cycloaddition Strategy, Acs Combinatorial Science, 2011, 13, 453-457.
  46. De Moliner, F.; Banfi, L.; Riva, R.; Basso, A., Beyond Ugi and Passerini Reactions: Multicomponent Approaches Based on Isocyanides and Alkynes as an Efficient Tool for Diversity Oriented Synthesis, Combinatorial Chemistry & High Throughput Screening, 2011, 14, 782-810.
  47. Basso, A.; Banfi, L.; Riva, R., Divergent Synthesis of Novel Five-Membered Heterocyclic Compounds by Base-Mediated Rearrangement of Acrylamides Derived from a Novel Isocyanide-Based Multicomponent Reaction, Molecules, 2011, 16, 8775-8787.
  48. Basso, A.; Banfi, L.; Guanti, G.; Riva, R.; Tosatti, P., Elaboration of Peptidomimetics Derived from a PADAM Approach: Synthesis of Polyfunctionalised 2(1H)-Pyrazinones via an Unexpected Aromatisation, Synlett, 2011, 2009-2012.
  49. Banfi, L.; Basso, A.; Giardini, L.; Riva, R.; Rocca, V.; Guanti, G., Tandem Ugi MCR/Mitsunobu Cyclization as a Short, Protecting-Group-Free Route to Benzoxazinones with Four Diversity Points, European Journal of Organic Chemistry, 2011, 100-109.
  50. Banfi, L.; Basso, A.; Cerulli, V.; Rocca, V.; Riva, R., Long-range diastereoselectivity in Ugi reactions of 2-substituted dihydrobenzoxazepines, Beilstein Journal of Organic Chemistry, 2011, 7, 976-979.
  51. Appendino, G.; Banfi, L., Molecular diversity and natural products, Molecular Diversity, 2011, 15, 291-292.
  52. Riva, R.; Banfi, L.; Basso, A.; Gandolfo, V.; Guanti, G., Enzymatically Asymmetrised Chiral Building Blocks for the Synthesis of Complex Natural Product Analogues: The Synthesis of Dynemicin Analogues from 2-(Quinolin-4-yl)propane-1,3-diol, European Journal of Organic Chemistry, 2010, 2768-2787.
  53. Riva, R.; Banfi, L.; Basso, A.; Cerulli, V.; Guanti, G.; Pani, M., A Highly Convergent Synthesis of Tricyclic N-Heterocycles Coupling an Ugi Reaction with a Tandem S(N)2 '-Heck Double Cyclization, Journal of Organic Chemistry, 2010, 75, 5134-5143.
  54. Moni, L.; Rossetti, S.; Scoponi, M.; Marra, A.; Dondoni, A., Immobilization of calix 4 arene-based glycoclusters on TiO2 nanoparticles via click Cu(I)-catalyzed azide-alkyne coupling, Chemical Communications, 2010, 46, 475-477.
  55. Moni, L.; Ciogli, A.; D'Acquarica, I.; Dondoni, A.; Gasparrini, F.; Marra, A., Synthesis of Sugar-Based Silica Gels by Copper-Catalysed Azide-Alkyne Cycloaddition via a Single-Step Azido-Activated Silica Intermediate and the Use of the Gels in Hydrophilic Interaction Chromatography, Chemistry-a European Journal, 2010, 16, 5712-5722.
  56. Guanti, G.; Banfi, L.; Basso, A.; Bondanza, L.; Guglieri, G.; Powles, K.; Riva, R., Optimized synthesis of phosphatidylserine, Amino Acids, 2010, 39, 367-373.
  57. De Moliner, F.; Crosignani, S.; Banfi, L.; Riva, R.; Basso, A., Synthesis of 5-Carboxamide-oxazolines with a Passerini-Zhu/Staudinger-Aza-Wittig Two-Step Protocol, Journal of Combinatorial Chemistry, 2010, 12, 613-616.
  58. Basso, A.; Banfi, L.; Riva, R., A Marriage of Convenience: Combining the Power of Isocyanide-Based Multicomponent Reactions with the Versatility of (Hetero)norbornene Chemistry, European Journal of Organic Chemistry, 2010, 1831-1841.
  59. Basso, A.; Banfi, L.; Guanti, G.; Riva, R., Straightforward stereoselective synthesis of polyfunctionalized cyclohexenols using a multicomponent approach, Tetrahedron, 2010, 66, 2390-2397.
  60. Banfi, L.; Riva, R.; Basso, A., Coupling Isocyanide-Based Multicomponent Reactions with Aliphatic or Acyl Nucleophilic Substitution Processes, Synlett, 2010, 23-41.
  61. Banfi, L.; Basso, A.; Cerulli, V.; Guanti, G.; Lecinska, P.; Monfardini, I.; Riva, R., Multicomponent synthesis of dihydrobenzoxazepinones, bearing four diversity points, as potential alpha-helix mimics, Molecular Diversity, 2010, 14, 425-442.
  62. Banfi, L.; Basso, A.; Casuscelli, F.; Guanti, G.; Naz, F.; Riva, R.; Zito, P., Synthesis of Novel Isochromene Derivatives by Tandem Ugi Reaction/Nucleophilic Substitution, Synlett, 2010, 85-88.


  • 21-7-2017: Marta Nola has obtained her master degree in Chemical Sciences with a mark of 108/110. Congratulations!
  • 5-7-2017: Hossny Ismail has obtained his international master degree in SERP-CHEM. Congratulations!
  • 16-6-2017: Giulio Less has obtained his master degree in Chemical Sciences with a mark of 106/110. Congratulations!
  • 15-6-2017: a video describing a photochemical reaction has been published on YouTube
  • 4-4-2017: Renata Riva and Andrea Basso have been habilitated for the role of full professor in Organic Chemistry. Congratulations!
  • 27-3-2017: Sergio Mulone has obtained the master degree in Chemical Sciences Magna cum Laude.
  • 21-3-2017: Luca Banfi has delivered an invited lecture at the minisymposium "Recent Advances in MCR Chemistry" hold in Groningen (NL). The title of the conference was "Multicomponent reactions starting from biobased components: a contribution to bioeconomy"
  • 24-2-2017: Samantha Caputo has been awarded the Ph.D. title in Science and Technology of Chemistry and Materials, with a thesis entitled "Topics in isocyanide-based multicomponent reactions (IMCRs): scope, selectivity and synthetic access to complex heterocyclic scaffolds". The defense was carried out at the University of Genova. Congratulations to Samantha and best wishes for her new job at the Italian Institute of Technology.
  • 10-2-2017: Alessandro Sannino has obtained the master degree in Chemical Sciences Magna cum Laude.


Ongoing external academic collaborations

  • The BOG group is involved in an interdisciplinary project named "From bio-inspired molecules to Alzheimer's disease prevention" funded by Fondazione Cariplo. For this project it collaborates with C.N.R., Macromolecular Institute (Milan, Genova) (C. D'Arrigo, S. Tomaselli, L. Ragona) and the "Mario Negri" Pharmacological Institute (G. Forloni).
  • University of Duesseldorf (T.J.J. Mueller) for the synthesis of fluorescent dyes through one-pot multicomponent-based processes.
  • Vrije Universiteit, Amsterdam (R. Orru, E. Ruijter) in a project involving coupling of biocatalysis with multicomponent reactions.
  • Edimburgh University (M. Bradley) for the development of biological tools activated by palladium.
  • IRCSS San Martino (M. Viale) in projects related to the development of new anti-cancer agents.
  • Universidad de Valladolid (A. Barbero) for using silicon-based MCRs on biobased substrates.
  • Università di Pavia (S. Protti) for photochemical multicomponent reactions.
  • University of Torino - Italian Institute of Technology (S. Giordani): attachment of fluorescent probes to nanomaterials.

Ongoing inter-departmental academic collaborations

  • F. Canepa, P. Riani: magnetic nanoparticles bound to enzymatically cleavable linkers.
  • D. Cavallo: synthesis of new additives for polymers.
  • M. Grotti: Analysis of selenium containing metabolites.
  • O. Monticelli: new biopolymers.

Ongoing collaborations with private companies

  • Active Cells
  • Bio Industria
  • Chemical Control
  • Lamberti group

  • How to join the group

    • If you are a master student at the university of Genova: there are open positions for your thesis in our group! Just contact us.
    • If you are a master student of a non-italian european university: you can come to Genova through the Erasmus+ programme either under the "study" or "traineeship" type of mobility, and perform part of the thesis (typically 5-10 months) in our laboratories. We have several established agreements (University at Duesseldorf, Barcelona University, Groningen University, Gent University, Leuven University, Pierre at Marie Curie University, Burgos University, Valladolid University and several others stipulated by our colleagues). If you are interested, please contact us well in advance (at least 6 months before the start of the stage period). Ask us for more informations.
    • If you are a prospective Ph.D. student, please note that you must apply by june 13 for the doctorate starting on november 1, 2017. You can find the call and other informations at Application is completely free. If you want to apply and desire to join our group, please let us know that before applying, since we can give you precious advice
    • If you are going to get a master degree and want to join us through an Erasmus + programme for post-lauream traineeship, it is OK, but please note that we require at least a 6 months stage, possibly not in summer (in august our laboratory is closed).
    • If you are a Ph.D. student in other universities and want to join us for a secondment period (at least 6 months) you are welcome, but please note that we have no possibility to give you any financial sponsorship. You need to be payed by our university or, in alternative, you can apply to the Erasmus programme or other inter-national funding schemes.
    • If you are searching for a post-doc position this will be much more difficult. At the moment we do not have open positions. If in the future we will have some, they will be posted on this site. Otherwise, please do not contact us for post-doc positions.



    Chiara Lambruschini was educated at the University of Genoa (Italy) where she received her Bachelor and Master Degree in Chemistry with hons in January 2007 and March 2009, respectively. During her master thesis she worked on the synthesis of polycyclic conjugated system and the study of their photochromic activity, under the supervision of Prof. G. Guanti and Prof. L. Banfi. In January 2010, she moved to the Italian Institute of Technology (Genoa, Italy) in the department of Drug Discovery and Development where she started her Ph.D. under the supervision of Dr. R. Scarpelli and Dr. C. Dalvit working in the field of fragment-based drug discovery. In particularly, she contributed to the development of the first application of a 19F NMR based functional assay to a membrane protein. She also worked on the synthetic evolution of the fragments identified from the assay against FAAH aiming at the discovery of new inhibitors as potential drugs for the treatment of pain and inflammation. During her Ph.D., she had the opportunity to work in the lab of Prof. T. Ritter at the Department of Chemistry and Chemical Biology at Harvard University (Boston, MA, USA), working on the development of a new synthetic approach for the PET tracer [18F]FAC involving a late-stage fluorination. In December 2013 she received her Ph.D. in Drug Discovery. In January 2014, she moved back to the DCCI as postdoctoral fellow, working in collaboration of the National Institute for Cancer Research (IST, Genoa, Italy) on the preparation by Ugi reaction of novel small-molecules as potential inhibitors of Stat3 dimer formation. Now she has an appointment up to may, 2018, for working on a project on the synthesis of polyphenols as potential drugs for Alzheimer's disease.



    Manuel Anselmo was born in Genova in 1990. He has a passion for Organic Chemistry since 2008, when, during his high school, he first met the BOG group and Prof. Luca Banfi who introduced him to DOS (Diversity Oriented Synthesis). Manuel achieved his bachelor in Chemistry magna cum laude in 2012, achieved at the University of Genoa. He contributed, under the supervision of Prof. Renata Riva and Prof. Luca Banfi, to a work concerning ‘a stereoselective and operationally simple synthesis of α-oxo- or α-hydroxy-γ-acylaminoamides and chromanes through a homo-PADAM strategy (homo-Passerini-amine deprotection-acyl migration)’. In 2013 he started his master thesis again in the BOG group, when he worked at a project concerning the ‘Highly Convergent Synthesis of Intensively Blue Emissive Furo[2,3-c]isoquinolines by a Palladium-Catalyzed Cyclization Cascade of Unsaturated Ugi Products’, under the supervision of Prof. Renata Riva and Dr. Lisa Moni. In 2014 he moved to Dusseldorf for spending 6 months (Erasmus Life Learning Program) working at the Heinrich-Heine Universitat, in the group of Thomas J. J. Muller. During this period he continued his master thesis work in collaboration with AK Muller, which is expert in the photophysical properties of organic molecules. Manuel achieved his master thesis in 2015, with the mark of 110/110. Shortly after, he started his PhD studies in the BOG group, under the supervision of Prof. Andrea Basso, studies which are currently ongoing and will presumably terminate in 2018. He is dedicating his doctoral research to visible light photoredox catalysis and flow chemistry, attempting to merge these topics with that of multicomponent reactions. He also has an appointment for October 2017, when he will move to Germany again for a traineeship, destination University of Regensburg. He in fact will continue his doctoral research in the group of Burkhard Konig, which has several years of expertise in visible light photoredox catalysis.





    Giulio Less obtained his bachelor degree in Chemistry and Chemical Technologies in Genoa on March 2015 with a thesis on chemical libraries' synthesis of chemical scaffolds obtained by asymmetric multicomponent reactions, under the supervision of Prof. L. Banfi and Doc. S. Caputo. He is attending the master course in Chemical Sciences in Genoa with a thesis on API's synthesis optimization and its initial phase of the scale-up process, in collaboration with a pharmaceutical industry and under the supervision of Prof. A. Basso and Doc. A. Moro.





    Pietro was born in 1993 and raised in Genoa. He attended the University of Genoa and received his Bachelor Degree in Chemistry with honors in October 2015. Currently he is working on his Master Thesis in the BioOrganic Chemistry Group in the Department of Chemistry and Industrial Chemistry under the supervision of Prof. Andrea Basso.



    Daniele Cartagenova, born in Genova on 15/07/1993 obtained his bachelor degree in “Chemistry and Chemical Technologies” in October 2015, with the highest mark (110/110 cum laudae) with a thesis on synthesis of pyrrole derivatives from nitrobutadienic building blocks, under the supervision of Prof. L. Bianchi. He is now attending master course in “Chemical Sciences” and working on a thesis on synthesis of enantiomerically pure oxygen heterocycles from biomass through coupling of biocatalysis and MCR, under the supervision of Prof. R. Riva and Prof. L. Moni.

    E-mail: daniele DOT cartagenova AT gmail DOT com




    Sirio Griva was born in La Spezia on 23/01/1993. He obtained a Bachelor Degree in “Biotechnology” on September 2015 (110 cum laude) with a thesis on "synthesis of potential inhibitors of antiapoptotic protein Bcl-xL by a multicomponent approach" under the supervision of Prof. Andrea Basso. Now he is enrolled in the Master Degree in “Chemical Sciences” and he works in the "multicomponent transformation of levulinic acid in nitrogen heterocycles" under the supervision of Prof. Luca Banfi.





    Hossny Ismail studied chemistry at Alexandria University (Egypt). He received his Bachelor in Chemistry degree with honors in July 2013. In February 2014, he joined RP Minerals as a junior research and development chemist. He was assigned to a pilot plant scale project involving the multi-step synthesis of fat-based quaternary ammonium salts. In 2015, Hossny joined SERP Chem Erasmus Mundus joint master course and got awarded an Erasmus Mundus scholarship. During his Master studies, he volunteered at the organic stereochemistry group of Adam Mickiewicz University where he worked on the synthesis of crowded aromatic dialdehydes under the supervision of Prof. Pawel Skowronek. Currently, Hossny is doing his master thesis at the bio-organic chemistry group of the University of Genoa under the supervision of Prof. Andrea Basso. He is working on the metal-catalyzed synthesis of isochromanones in batch and under continuous flow conditions. Alongside academics, Hossny co-founded an international student chapter of the American Chemical Society at Alexandria University and he serves as a graduate student advisor up to date.