Fèlix Urpí, Ph.D.
Affiliations: | 1988- | Organic Chemistry | Universitat de Barcelona, Barcelona, Cataluña, Spain |
Area:
Total synthesis, synthetic methodology, computational chemistryWebsite:
http://www.qo.ub.edu/personals/furpi/es/Google:
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Publications
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| Trigili C, Pera B, Barbazanges M, et al. (2011) Mechanism of action of the cytotoxic macrolides amphidinolide X and J. Chembiochem : a European Journal of Chemical Biology. 12: 1027-30 |
| Llàcer E, Urpí F, Vilarrasa J. (2009) Efficient approach to fluvirucins B2-B5, Sch 38518, and Sch 39185. First synthesis of their aglycon, via CM and RCM reactions. Organic Letters. 11: 3198-201 |
| Burés J, Martín M, Urpí F, et al. (2009) Catalytic Staudinger-Vilarrasa reaction for the direct ligation of carboxylic acids and azides. The Journal of Organic Chemistry. 74: 2203-6 |
| Rodríguez-Escrich C, Urpí F, Vilarrasa J. (2008) Stereocontrolled total synthesis of amphidinolide X via a silicon-tethered metathesis reaction. Organic Letters. 10: 5191-4 |
| Olivella A, Rodríguez-Escrich C, Urpí F, et al. (2008) Michael reactions of titanium enolates of glycolic acid derivatives with the Weinreb and morpholine amides of acrylic acid. The Journal of Organic Chemistry. 73: 1578-81 |
| Rodríguez-Escrich C, Olivella A, Urpí F, et al. (2007) Toward a total synthesis of amphidinolide X and Y. The tetrahydrofuran-containing fragment C12-C21. Organic Letters. 9: 989-92 |
| Solsona JG, Romea P, Urpí F, et al. (2003) Highly stereoselective aldol reactions of titanium enolates from lactate-derived chiral ketones. Organic Letters. 5: 519-22 |
| Larrosa I, Romea P, Urpí F, et al. (2002) Unprecedented highly stereoselective alpha- and beta-C-glycosidation with chiral titanium enolates. Organic Letters. 4: 4651-4 |