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Results: 1-11 |
Results: 11
Dithiourea ligands in the rhodium-catalyzed hydride-transfer reduction of ketones - A theoretical and experimental approach
Authors: Bernard, M Delbecq, F Fache, F Sautet, P Lemaire, M
Citation: M. Bernard et al., Dithiourea ligands in the rhodium-catalyzed hydride-transfer reduction of ketones - A theoretical and experimental approach, EUR J ORG C, (8), 2001, pp. 1589-1596
New perfluoroalkylated cinchona derivatives: synthesis and use in base-catalysed Diels-Alder reactions
Authors: Fache, F Piva, O
Citation: F. Fache et O. Piva, New perfluoroalkylated cinchona derivatives: synthesis and use in base-catalysed Diels-Alder reactions, TETRAHEDR L, 42(33), 2001, pp. 5655-5657
Polythioureas: Main chain chiral polymers in hydride transfer hydrogenation
Authors: Touchard, F Fache, F Lemaire, M
Citation: F. Touchard et al., Polythioureas: Main chain chiral polymers in hydride transfer hydrogenation, EUR J ORG C, (22), 2000, pp. 3787-3792
Influence of the drying technique of silica gels on the enzymatic activityof encapsulated lipase
Authors: Pierre, M Buisson, P Fache, F Pierre, A
Citation: M. Pierre et al., Influence of the drying technique of silica gels on the enzymatic activityof encapsulated lipase, BIOCATAL B, 18(3), 2000, pp. 237-251
Catalytic asymmetric hydride transfer reduction of ketones with rhodium and chiral diamine ligands: Approach of the active species structure by DFT calculations
Authors: Bernard, M Delbecq, F Sautet, P Fache, F Lemaire, M
Citation: M. Bernard et al., Catalytic asymmetric hydride transfer reduction of ketones with rhodium and chiral diamine ligands: Approach of the active species structure by DFT calculations, ORGANOMETAL, 19(26), 2000, pp. 5715-5722
An environmentally benign access to carbamates and ureas
Authors: Vauthey, I Valot, F Gozzi, C Fache, F Lemaire, M
Citation: I. Vauthey et al., An environmentally benign access to carbamates and ureas, TETRAHEDR L, 41(33), 2000, pp. 6347-6350
Recent progress in asymmetric heterogeneous catalysis: use of polymer-supported catalysts
Authors: Saluzzo, C ter Halle, R Touchard, F Fache, F Schulz, E Lemaire, M
Citation: C. Saluzzo et al., Recent progress in asymmetric heterogeneous catalysis: use of polymer-supported catalysts, J ORGMET CH, 603(1), 2000, pp. 30-39
Nitrogen-containing ligands for asymmetric homogeneous and heterogeneous catalysis
Authors: Fache, F Schulz, E Tommasino, ML Lemaire, M
Citation: F. Fache et al., Nitrogen-containing ligands for asymmetric homogeneous and heterogeneous catalysis, CHEM REV, 100(6), 2000, pp. 2159-2231
Ureas and thioureas as Rh-ligands for the enantioselective hydride transfer reduction of acetophenone
Authors: Touchard, F Bernard, M Fache, F Lemaire, M
Citation: F. Touchard et al., Ureas and thioureas as Rh-ligands for the enantioselective hydride transfer reduction of acetophenone, J MOL CAT A, 140(1), 1999, pp. 1-11
Gas-phase selective N-alkylation of amines with alcohols over gamma-alumina
Authors: Valot, F Fache, F Jacquot, R Spagnol, M Lemaire, M
Citation: F. Valot et al., Gas-phase selective N-alkylation of amines with alcohols over gamma-alumina, TETRAHEDR L, 40(19), 1999, pp. 3689-3692
Activated imines and aminal derivatives: Potential precursors of beta-amino acids
Authors: Milenkovic, A Fache, F Faure, R Lemaire, M
Citation: A. Milenkovic et al., Activated imines and aminal derivatives: Potential precursors of beta-amino acids, SYN COMMUN, 29(9), 1999, pp. 1535-1546
Risultati: 1-11 |