Prior to the University of Vienna

  • 15. Nitrate reduction enables safer aryldiazonium chemistry. Mateos, J.,† Schulte, T., † Behera, D., Leutzsch, M., Altun, A., Sato, T. Schnegg, A., Neese, F., Ritter, T.*, Science, 2024, 384, 446–452. DOI: 10.1126/science.adn7006.
  • 14. Catalytic asymmetric defluorinative allylation of silyl enol ethers. Duran, J., Mateos, J., Moyano, A., Companyó, X.*, Chem. Sci., 2023, 14, 7147–7153. DOI: 10.1039/D3SC01498C.
  • 13. Unveiling the impact of the light source and steric factors on [2+2]-heterocycloaddition reactions. Mateos, J., Rigodanza, F., Costa, P., Natali, M., Vega-Peñaloza, Fresch, E., Collini, E., A., Bonchio, M., Sartorel, A., Dell’Amico, L.*, Nat. Synth., 2023, 2, 26–36. DOI: 10.1038/s44160-022-00191-5.
  • 12. Halloysite nanotubes as bimodal Lewis/Brønsted acid heterogeneous catalysts for the synthesis of heterocyclic compounds. Yu, J., Mateos, J., Carraro, M.*, Nanomaterials, 2023, 13, 394. DOI 10.3390/nano13030394.
  • 11. Unlocking the synthetic potential of light-excited aryl ketones: applications in direct photochemistry and photoredox catalysis. Mateos, J., Cuadros, S., Vega-Peñaloza, A., Dell’Amico, L.*, SynLett, 2021, 33, 116–128. DOI: 10.1055/a-1403-4613.
  • 10. High site selectivity in electrophilic aromatic substitutions: mechanism of C–H thianthrenation. Julia, F., † Shao, Q., † Duan, M.†, Plutschack, M., Berger, F., Mateos, J., Lu, C., Xue, X-S., Houk, K.N.,* Ritter, T.*, J. Am. Chem. Soc., 2021, 143, 16041–16054. DOI: 10.1021/jacs.1c06281.
  • 9. Radical a-trifluoromethoxylation of ketones under batch and flow conditions by means of organic Photoredox Catalysis. Duhail, T.,† Bortolato, T.,† Mateos, J., Anselmi, E., Jelier, B., Togni, A., Magnier, E.,* Dagousset, G.,* Dell’Amico, L.*, Org. Lett., 2021, 23, 7088–7093. DOI: 10.1021/acs.orglett.1c02494.
  • 8. A rational approach to organo-photocatalysis. novel designs and structure-property-relationships. Vega-Peñaloza, A., Mateos, J., Companyó, X., Escudero-Casao, M., Dell’Amico, L.*, Angew. Chem. Int. Ed., 2021, 3, 1082–1097. DOI: 10.1002/anie.202006416.
  • 7. Exploiting the reactivity of oxindole silyl enol ethers in the Paternò-Büchi dearomatisation-process. Franceschi, P., Mateos, J., Vega-Peñaloza, A.*, Dell’Amico, L.*, Eur. J. Org. Chem., 2020, 43, 6718–6722. DOI: 10.1002/ejoc.202001057.
  • 6. A visible-light Paternò-Büchi dearomatisation-process towards the Construction of oxetoindolinic polycycles. Mateos, J.,† Vega-Peñaloza, A.,† Franceschi, P.,† Rigodanza, F., Andreetta, P., Companyó, X.*, Pelosi, G., Bonchio, M., Dell’Amico, L.*, Chem. Sci., 2020, 11, 6532–6538. DOI: 10.1039/D0SC01569E.
  • 5. Naphthochromenones: organic bimodal photocatalysts engaging in both oxidative and reductive quenching processes. Mateos, J.,† Rigodanza, F.,† Vega-Peñaloza, A., Sartorel, A., Natali, M., Bortolato, T., Pelosi, G., Companyó, X., Bonchio, M., Dell’Amico, L.*, Angew. Chem. Int. Ed., 2020, 41, 1302–1312. DOI: 10.1002/anie.201912455.
  • 4. Microfluidic light-driven synthesis of tetracyclic molecular architectures. Mateos, J., Meneghini, N., Bonchio, M., Marino, N., Carofiglio, T., Companyó, X.*, Dell’Amico, L.*, Beilstein J. Org. Chem., 2018, 14, 2418–2424. DOI: 10.3762/bjoc.14.219.
  • 3. Transition metal-free CO2 fixation into new carbon-carbon bonds. Cherubini-Celli, A., Mateos, J., Bonchio, M.*, Dell’Amico, L.*, Companyó, X.*, ChemSusChem, 2018, 11, 3056–3070. DOI: 10.1002/cssc.201801063.
  • 2. Luminescent supramolecular heterometallic macrocycles and their encapsulation on cholate gels. Gavara, R.*, Mateos, J., Sabaté, F., Belda, R., Llinares, J. M., García-España, E.*, Rodríguez, L.* Eur. J. Inorg. Chem., 2018, 4550–4555. DOI: 10.1002/ejic.201800697. 
  • 1. A microfluidic photoreactor enables 2-methylbenzophenone light-driven reactions with superior performance. Mateos, J., Cherubini-Celli, A., Carofiglio, T., Bonchio, M., Marino, N., Companyó, X.*, Dell’Amico, L.*, Chem. Commun., 2018, 54, 6820–6823. DOI: 10.1039/C8CC01373J.