| The asymmetric Michael addition reactions using chiral imines J d'Angelo, D Desma le, F Dumas, A Guingant Tetrahedron, asymmetry 3 (4), 459-505, 1992 | 307 | 1992 |
| Tricyclic sesquiterpenes from marine origin F Le Bideau, M Kousara, L Chen, L Wei, F Dumas Chemical Reviews 117 (9), 6110-6159, 2017 | 118 | 2017 |
| Brazilian red propolis: Chemical composition and antibacterial activity determined using bioguided fractionation LC Rufatto, P Luchtenberg, C Garcia, C Thomassigny, S Bouttier, ... Microbiological research 214, 74-82, 2018 | 117 | 2018 |
| Investigating the π-Facial Discrimination Phenomenon in the Conjugate Addition of Amines to Chiral Crotonates: A Convenient Basis for the Rational Design of Chiral Auxiliaries F Dumas, B Mezrhab, J d'Angelo, C Riche, A Chiaroni The Journal of Organic Chemistry 61 (7), 2293-2304, 1996 | 107 | 1996 |
| Functionalization of Single-Wall Carbon Nanotubes by Tandem High-Pressure/Cr(CO)6 Activation of Diels−Alder Cycloaddition C Ménard-Moyon, F Dumas, E Doris, C Mioskowski Journal of the American Chemical Society 128 (46), 14764-14765, 2006 | 106 | 2006 |
| New chiral auxiliaries: their use in the asymmetric hydrogenation of. beta.-acetamidocrotonates D Potin, F Dumas, J D'Angelo Journal of the American Chemical Society 112 (9), 3483-3486, 1990 | 97 | 1990 |
| Numismatique médiévale, monnaies et documents d'origine française M Bompaire, F Dumas Brepols, 2000 | 83 | 2000 |
| A new access to homoerythrina alkaloids MA Le Dreau, D Desmaele, F Dumas, J d'Angelo The Journal of Organic Chemistry 58 (11), 2933-2935, 1993 | 61 | 1993 |
| Experimental demonstration of the carbamazepine crystallization from non-photochemical laser-induced nucleation in acetonitrile and methanol A Ikni, B Clair, P Scouflaire, S Veesler, JM Gillet, N El Hassan, F Dumas, ... Crystal growth & design 14 (7), 3286-3299, 2014 | 59 | 2014 |
| Crystal structure of crotonic acid ester of the highly potent chiral auxiliary trans-2-[1-(2-naphthyl)-1-methylethyl] cyclohexanol: direct evidence for the critical … B Mezrhab, F Dumas, J d'Angelo, C Riche The Journal of Organic Chemistry 59 (2), 500-503, 1994 | 57 | 1994 |
| Cephalotaxus alkaloids J Pérard-Viret, L Quteishat, R Alsalim, J Royer, F Dumas The alkaloids: chemistry and biology 78, 205-352, 2017 | 54 | 2017 |
| High pressure activation in the asymmetric Michael addition of chiral imines to alkyl and aryl crotonates C Camara, D Joseph, F Dumas, J d'Angelo, A Chiaroni Tetrahedron letters 43 (8), 1445-1448, 2002 | 43 | 2002 |
| Organo-catalyzed/initiated ring opening co-polymerization of cyclic anhydrides and epoxides: an emerging story D Ryzhakov, G Printz, B Jacques, S Messaoudi, F Dumas, S Dagorne, ... Polymer Chemistry 12 (20), 2932-2946, 2021 | 40 | 2021 |
| Green synthesis, antioxidant and antibacterial activities of 4-aryl-3, 4-dihydropyrimidinones/thiones derivatives of curcumin. Theoretical calculations and mechanism study N Khaldi-Khellafi, M Makhloufi-Chebli, D Oukacha-Hikem, ST Bouaziz, ... Journal of Molecular Structure 1181, 261-269, 2019 | 37 | 2019 |
| Synthesis, structural analysis and anticonvulsant activity of a ternary Cu (II) mononuclear complex containing 1, 10-phenanthroline and the leading antiepileptic drug valproic acid MSI Veitía, F Dumas, G Morgant, JRJ Sorenson, Y Frapart, A Tomas Biochimie 91 (10), 1286-1293, 2009 | 36 | 2009 |
| Intramolecular Michael addition of chiral imines to enoates: a new asymmetric carbocyclization reaction F Dumas, J d'Angelo Tetrahedron: Asymmetry 1 (3), 167-170, 1990 | 32 | 1990 |
| Enantioselective synthesis of the ester side chain of homoharringtonine L Keller, F Dumas, J d'Angelo Tetrahedron Letters 42 (10), 1911-1913, 2001 | 30 | 2001 |
| High pressure induced mukaiyama type aldol reaction of bis trimethylsilyl ketene acetals M Bellassoued, E Reboul, F Dumas Tetrahedron letters 38 (32), 5631-5634, 1997 | 27 | 1997 |
| Improved Asymmetric Synthesis of 8-Arylmenthols D Potin, F Dumas, J Maddaluno Synthetic communications 20 (18), 2805-2813, 1990 | 27 | 1990 |
| Synthesis and biological evaluation of new substituted hantzsch thiazole derivatives from environmentally benign one-pot synthesis using silica supported tungstosilisic acid as … H Bouherrou, A Saidoun, A Abderrahmani, L Abdellaziz, Y Rachedi, ... Molecules 22 (5), 757, 2017 | 26 | 2017 |
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