17. “Click Processes Orthogonal to CuAAC and SuFEx Forge Selectively Modifiable Fluorescent Links” Paioti, P. H. S.; Lounsbury, K. E.; Romiti, F.; Formica, M.; Bauer, V.; Zandonella, C.; Hackey, M. E.; del Pozo, J.; Hoveyda, A. H.* Nat. Chem. 2023, DOI: 10.1038/s41557-023-01386-9.
16. “Streamlined Strategy for Scalable and Enantioselective Total Syntheses of the Eburnane Alkaloids” Ramakrishna, G. V.; Pop, L. P.; Latif, Z.; Suryadevara, H. K. V.; Santo, L.; Romiti, F.* J. Am. Chem. Soc. 2023, 145, 20062−20072. [HTML] [PDF]
15. “Diastereo- and Enantioselective Synthesis of Compounds with a Trifluoromethyl- and Fluoro-Substituted Carbon Centre” Xu, S.; del Pozo, J.; Romiti, F.; Fu, Y.; Mai, B. K.; Morrison, R. J.; Lee, K.; Hu, S.; Koh, M. J.; Lee, J.; Li, X.; Liu, P.*; Hoveyda, A. H.* Nat. Chem. 2022, 14, 1459−1469.
14. “Convergent Synthesis of the C115. “Convergent Synthesis of the C1–C29 Framework of Amphidinolide F” Romiti, F.; Decultot, L.; Clark, J. S.* J. Org. Chem. 2022, 87, 8126−8141.
13. “E– and Z-Trisubstituted Macrocyclic Alkenes for Natural Product Synthesis and Skeletal Editing” Mu, Y.; Hartrampf, F. W. W.; Yu, E. C.; Lounsbury, K. E.; Schrock, R. R.; Romiti, F.*; Hoveyda, A. H.* Nat. Chem. 2022, 14, 640–649. *co-corresponding authors [HTML] [PDF]
12. “Streamlined Catalytic Enantioselective Synthesis of α-Substituted β,γ-Unsaturated Ketones and Either of the Corresponding Tertiary Homoallylic Alcohol Diastereomers” del Pozo, J.§; Zhang, S.§; Romiti, F.§; Xu, S.; Conger, R. P.; Hoveyda, A. H. * J. Am. Chem. Soc. 2020, 142, 18200–18212. §These authors contributed equally
11. “A Catalytic Approach for Enantioselective Synthesis of Homoallylic Alcohols Bearing a Z-Alkenyl Chloride. A Concise and Protecting Group-Free Synthesis of Mycothiazole” Morrison, R. J.; van der Mei, F. W.; Romiti, F.*; Hoveyda, A. H.* J. Am. Chem. Soc. 2020, 142, 436–447. *co-corresponding authors [HTML] [PDF]
10. “Catalytic Enantioselective Conjugate Addition of Stereodefined Di- and Trisubstituted Alkenylaluminum Compounds to Acyclic Enones” McGrath, K. P.; Hubbell, A. K.; Zhou, Y.; Padín Santos, D.; Torker, S.; Romiti, F.*; Hoveyda, A. H.* Adv. Synth. Catal. 2020, 362, 370–375. Special Issue: Dedicated to Eric N. Jacobsen on the occasion of his 60th birthday. *co-corresponding authors [HTML] [PDF]
9. “Catalytic Enantioselective Boryl and Silyl Substitution with Trifluoromethyl Alkenes: Scope, Utility, and Mechanistic Nuances of Cu–F ß-Elimination” Paioti, P. H. S.; del Pozo, J.; Mikus, M. S.; Lee, J.; Koh, M. J.; Romiti, F.; Torker, S.; Hoveyda, A. H.* J. Am. Chem. Soc. 2019, 141, 19917–19934.
8. “Different Strategies for Designing Dual-Catalytic Enantioselective Processes: From Fully Cooperative to Non-cooperative Systems” Romiti, F.; del Pozo, J.; Paioti, P. H. S.; Gonsales, S. A.; Li, X.; Hartrampf, F. W. W.; Hoveyda, A. H.* J. Am. Chem. Soc. 2019, 141, 17952–17961.
7. “Catalytic Enantioselective Synthesis of Allylic Boronates Bearing a Trisubstituted Alkenyl Fluoride and Related Derivatives” Akiyama, S. ; Kubota, K.; Mikus, M. S.; Paioti, P. H. S.; Romiti, F.; Liu, Q.; Zhou, Y.; Hoveyda, A. H.*; Ito, H.* Angew. Chem. Int. Ed. 2019, 58, 11998–12003.
6. “Delayed Catalyst Function Enables Direct Enantioselective Conversion of Nitriles to NH2-Amines” Zhang, S.§; del Pozo, J.§; Romiti, F.§; Mu, Y.; Torker, S.; Hoveyda, A. H.* Science 2019, 364, 45–51. §These authors contributed equally
5. “Catalytic Diastereo- and Enantioselective Additions of Versatile Allyl Groups to N–H Ketimines” H. Jang, F. Romiti, S. Torker, A. H. Hoveyda* Nat. Chem. 2017, 9, 1269–1275.
4. “Kinetically Controlled E-selective Catalytic Olefin Metathesis” Nguyen, T. T.; Koh, M. J.; Shen, X.; Romiti, F.; Schrock, R. R.; Hoveyda, A. H.* Science 2016, 352, 569–575.
3. “Synthesis of the A−D Ring System of the Gambieric Acids” Clark, J. S.*; Romiti, F.; Sieng, B.; Paterson, L.; Stewart, A.; Chaudhury, S.; Thomas, L. H. Org. Lett. 2015, 17, 4694–4697.
2. “Synthesis of Cyclopropyl-Substituted Furans by Brønsted Acid Promoted Cascade Reactions” Clark, J. S.*; Romiti, F.; Hogg, K. F.; Hamid, M. H. S. A.; Richter, S. C.; Boyer, A.; Redman, J. C.; Farrugia, L. J. Angew. Chem. Int. Ed. 2015, 54, 5744–5747.
1. “Total Syntheses of Amphidinolides T1, T3, and T4” Clark, J. S.*; Romiti, F. Angew. Chem. Int. Ed. 2013, 52, 10072–10075.