| Absolute configuration of chirally deuterated neopentane J Haesler, I Schindelholz, E Riguet, CG Bochet, W Hug Nature 446 (7135), 526-529, 2007 | 232 | 2007 |
| A peptide nucleic acid− neamine conjugate that targets and cleaves HIV-1 TAR RNA inhibits viral replication E Riguet, S Tripathi, B Chaubey, J Désiré, VN Pandey, JL Décout Journal of medicinal chemistry 47 (20), 4806-4809, 2004 | 95 | 2004 |
| Photosensitized addition of isopropanol to furanones in a 365 nm UV-LED microchip O Shvydkiv, A Yavorskyy, K Nolan, A Youssef, E Riguet, N Hoffmann, ... Photochemical & Photobiological Sciences 9, 1601-1603, 2010 | 60 | 2010 |
| Neamine dimers targeting the HIV-1 TAR RNA E Riguet, J Désiré, O Boden, V Ludwig, M Göbel, C Bailly, JL Décout Bioorganic & medicinal chemistry letters 15 (21), 4651-4655, 2005 | 57 | 2005 |
| A route for preparing new neamine derivatives targeting HIV-1 TAR RNA E Riguet, J Désiré, C Bailly, JL Décout Tetrahedron 60 (37), 8053-8064, 2004 | 41 | 2004 |
| Enantioselective Organocatalytic Friedel–Crafts Alkylation Reaction of Indoles with 5-Hydroxyfuran-2(5H)-one: Access to Chiral γ-Lactones and γ-Lactams via a … E Riguet The Journal of Organic Chemistry 76 (20), 8143-8150, 2011 | 39 | 2011 |
| Sulfonated surfactants obtained from furfural A Gassama, C Ernenwein, A Youssef, M Agach, E Riguet, S Marinković, ... Green chemistry 15 (6), 1558-1566, 2013 | 33 | 2013 |
| Novel guanidinyl pyrrolidine salt-based bifunctional organocatalysts: application in asymmetric conjugate addition of malonates to enones E Riguet Tetrahedron Letters 50 (29), 4283-4285, 2009 | 31 | 2009 |
| New safety-catch photolabile protecting group E Riguet, CG Bochet Organic letters 9 (26), 5453-5456, 2007 | 26 | 2007 |
| Synthesis of chiral γ-lactones by one-pot sequential enantioselective organocatalytic michael addition of boronic acids and diastereoselective intramolecular Passerini reaction M Bos, E Riguet The Journal of Organic Chemistry 79 (22), 10881-10889, 2014 | 25 | 2014 |
| Iridium-catalysed asymmetric allylic alkylation of benzofuran γ-lactones followed by heteroaromatic Cope rearrangement: study of an unusual reaction sequence M Bos, E Riguet Chemical communications 53 (36), 4997-5000, 2017 | 21 | 2017 |
| High‐resolution and high‐sensitivity 2D homonuclear J‐resolved NMR spectroscopy A Martinez, F Bourdreux, E Riguet, JM Nuzillard Magnetic Resonance in Chemistry 50 (1), 28-32, 2012 | 19 | 2012 |
| N. Hoffmann in Comprehensive Organic Synthesis, Vol. 5 E Riguet Elsevier, Amsterdam,, 2014 | 9 | 2014 |
| Synthetic radical photochemistry E Riguet, N Hoffmann Encyclopedia of Radicals in Chemistry, Biology and Materials, 2012 | 8 | 2012 |
| Broadening the reaction scope of unprotected aldoses via their corresponding nitrones: 1, 3-dipolar cycloadditions with alkenes G Messire, F Massicot, L Pascual, E Riguet, JL Vasse, JB Behr Organic & Biomolecular Chemistry 18, 5708-5725, 2020 | 7 | 2020 |
| Organocatalytic Gram-Scale Synthesis and Alkylation of Heteroaryl and Electron-Rich Aryl α-Substituted γ-Lactones M Bos, F Buttard, A Vallée, E Riguet Synthesis 51 (16), 3151-3159, 2019 | 6 | 2019 |
| cis-Dihydroxylated α-Trifluoromethylated N, O-Acetal from l-Tartaric Acid: Synthesis of Tetrasubstituted Stereocenter via Diastereoselective Pictet-Spengler Cyclization of N … A Ben Jamaa, M Latrache, E Riguet, F Grellepois The Journal of Organic Chemistry 85, 9585-9598, 2020 | 5 | 2020 |
| Organocatalytic enantioselective allylic alkylation of α-aryl γ-lactones: an approach to densely functionalized quaternary stereocentres M Mando, F Grellepois, E Riguet Chemical Communications 56, 6640-6643, 2020 | 5 | 2020 |
| Singlet-oxygen-induced rearrangement of furan derivatives N Charbonnet, E Riguet, CG Bochet Synlett 2011 (15), 2231-2233, 2011 | 4 | 2011 |
| Organocatalyzed Asymmetric Allylic Alkylation Enables Synthesis of Chiral γ-Lactones Bearing Vicinal Tertiary and Quaternary Stereocenters M Mando, M Fares, C Kowandy, F Grellepois, E Riguet Organic Letters 24 (29), 5351-5355, 2022 | 3 | 2022 |
