Elena Arceo
Affiliations: | 2010 | TCI |
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| Silvi M, Arceo E, Jurberg ID, et al. (2015) Enantioselective organocatalytic alkylation of aldehydes and enals driven by the direct photoexcitation of enamines. Journal of the American Chemical Society. 137: 6120-3 |
| Arceo E, Montroni E, Melchiorre P. (2014) Photo-organocatalysis of atom-transfer radical additions to alkenes. Angewandte Chemie (International Ed. in English). 53: 12064-8 |
| Arceo E, Bahamonde A, Bergonzini G, et al. (2014) Enantioselective direct α-alkylation of cyclic ketones by means of photo-organocatalysis Chemical Science. 5: 2438-2442 |
| Arceo E, Jurberg ID, Alvarez-Fernández A, et al. (2013) Photochemical activity of a key donor-acceptor complex can drive stereoselective catalytic α-alkylation of aldehydes. Nature Chemistry. 5: 750-6 |
| Cassani C, Martín-Rapún R, Arceo E, et al. (2013) Synthesis of 9-amino(9-deoxy)epi cinchona alkaloids, general chiral organocatalysts for the stereoselective functionalization of carbonyl compounds. Nature Protocols. 8: 325-44 |
| Tian X, Cassani C, Liu Y, et al. (2011) Diastereodivergent asymmetric sulfa-Michael additions of α-branched enones using a single chiral organic catalyst. Journal of the American Chemical Society. 133: 17934-41 |
| Liu Y, Nappi M, Arceo E, et al. (2011) Asymmetric catalysis of Diels-Alder reactions with in situ generated heterocyclic ortho-quinodimethanes. Journal of the American Chemical Society. 133: 15212-8 |
| Arceo E, Ellman JA, Bergman RG. (2010) Rhenium-catalyzed didehydroxylation of vicinal diols to alkenes using a simple alcohol as a reducing agent. Journal of the American Chemical Society. 132: 11408-9 |
| Arceo E, Ellman JA, Bergman RG. (2010) A direct, biomass-based synthesis of benzoic acid: formic acid-mediated deoxygenation of the glucose-derived materials quinic acid and shikimic acid. Chemsuschem. 3: 811-3 |
| Arceo E, Marsden P, Bergman RG, et al. (2009) An efficient didehydroxylation method for the biomass-derived polyols glycerol and erythritol. Mechanistic studies of a formic acid-mediated deoxygenation. Chemical Communications (Cambridge, England). 3357-9 |