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Results: 1-11 |
Results: 11
Optimization of new chiral ligands for the copper-catalysed enantioselective conjugate addition of Et2Zn to nitroolefins by high-throughput screeningof a parallel library
Authors: Ongeri, S Piarulli, U Jackson, RFW Gennari, C
Citation: S. Ongeri et al., Optimization of new chiral ligands for the copper-catalysed enantioselective conjugate addition of Et2Zn to nitroolefins by high-throughput screeningof a parallel library, EUR J ORG C, (4), 2001, pp. 803-807
Enantioselective binding of dipeptides using acyclic receptors
Authors: Botana, E Ongeri, S Arienzo, R Demarcus, M Frey, JG Piarulli, U Potenza, D Gennari, C Kilburn, JD
Citation: E. Botana et al., Enantioselective binding of dipeptides using acyclic receptors, CHEM COMMUN, (15), 2001, pp. 1358-1359
Discovery of a new efficient chiral ligand for copper-catalyzed enantioselective Michael additions by high-throughput screening of a parallel library
Authors: Chataigner, I Gennari, C Ongeri, S Piarulli, U Ceccarelli, S
Citation: I. Chataigner et al., Discovery of a new efficient chiral ligand for copper-catalyzed enantioselective Michael additions by high-throughput screening of a parallel library, CHEM-EUR J, 7(12), 2001, pp. 2628-2634
A carbonylative cross-coupling strategy to the total synthesis of the sarcodictyins: preliminary studies and synthesis of a cyclization precursor
Authors: Ceccarelli, SM Piarulli, U Telser, J Gennari, C
Citation: Sm. Ceccarelli et al., A carbonylative cross-coupling strategy to the total synthesis of the sarcodictyins: preliminary studies and synthesis of a cyclization precursor, TETRAHEDR L, 42(42), 2001, pp. 7421-7425
Synthetic studies on the sarcodictyins: synthesis of fully functionalized cyclization precursors
Authors: Ceccarelli, SM Piarulli, U Gennari, C
Citation: Sm. Ceccarelli et al., Synthetic studies on the sarcodictyins: synthesis of fully functionalized cyclization precursors, TETRAHEDRON, 57(40), 2001, pp. 8531-8542
Discovery of a new efficient chiral ligand for copper-catalyzed enantioselective Michael additions by high-throughput screening of a parallel library
Authors: Chataigner, I Gennari, C Piarulli, U Ceccarelli, S
Citation: I. Chataigner et al., Discovery of a new efficient chiral ligand for copper-catalyzed enantioselective Michael additions by high-throughput screening of a parallel library, ANGEW CHEM, 39(5), 2000, pp. 916
Effect of ligands and additives on the palladium-promoted carbonylative coupling of vinyl stannanes and electron-poor enol triflates
Authors: Ceccarelli, S Piarulli, U Gennari, C
Citation: S. Ceccarelli et al., Effect of ligands and additives on the palladium-promoted carbonylative coupling of vinyl stannanes and electron-poor enol triflates, J ORG CHEM, 65(19), 2000, pp. 6254-6256
Solid-phase synthesis of peptides containing reverse-turn mimetic bicycliclactams
Authors: Gennari, C Mielgo, A Potenza, D Scolastico, C Piarulli, U Manzoni, L
Citation: C. Gennari et al., Solid-phase synthesis of peptides containing reverse-turn mimetic bicycliclactams, EUR J ORG C, (2), 1999, pp. 379-388
Ureas: New efficient Lewis base catalysts for the allylation of aldehydes
Authors: Chataigner, I Piarulli, U Gennari, C
Citation: I. Chataigner et al., Ureas: New efficient Lewis base catalysts for the allylation of aldehydes, TETRAHEDR L, 40(18), 1999, pp. 3633-3634
A trifunctional steroid-based scaffold for combinatorial chemistry
Authors: Barry, JF Davis, AP Perez-Payas, MN Elsegood, MRJ Jackson, RFW Gennari, C Piarulli, U Gude, M
Citation: Jf. Barry et al., A trifunctional steroid-based scaffold for combinatorial chemistry, TETRAHEDR L, 40(14), 1999, pp. 2849-2852
Synthetic studies on sarcodictyins and eleutherobin: Synthesis of fully functionalized cyclization precursors
Authors: Ceccarelli, S Piarulli, U Gennari, C
Citation: S. Ceccarelli et al., Synthetic studies on sarcodictyins and eleutherobin: Synthesis of fully functionalized cyclization precursors, TETRAHEDR L, 40(1), 1999, pp. 153-156
Risultati: 1-11 |