Stéphane Raeppel
Publications by Year
Research Areas
Asymmetric Synthesis and Catalysis, Chemical synthesis and alkaloids, Liver physiology and pathology, Catalytic Alkyne Reactions, Histone Deacetylase Inhibitors Research
Most-Cited Works
- → Discovery of N-(2-Aminophenyl)-4-[(4-pyridin-3-ylpyrimidin-2-ylamino)methyl]benzamide (MGCD0103), an Orally Active Histone Deacetylase Inhibitor(2008)108 cited
- → Lewis acid-catalyzed Mannich type reactions with potassium organotrifluoroborates(2004)58 cited
- → Amphoteric Character of 2-Vinyloxiranes: Synthetic Equivalents ofβ,γ-Unsaturated Aldehydes and a Vinylogous Enolate(2000)56 cited
- → N-(4-(6,7-Disubstituted-quinolin-4-yloxy)-3-fluorophenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: A novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors(2009)50 cited
- → Design and synthesis of 4-[(s-triazin-2-ylamino)methyl]-N-(2-aminophenyl)-benzamides and their analogues as a novel class of histone deacetylase inhibitors(2007)35 cited
- → N-(3-fluoro-4-(2-arylthieno[3,2-b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: A novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors(2009)34 cited
- → Substituted N-(2-aminophenyl)-benzamides, (E)-N-(2-aminophenyl)-acrylamides and their analogues: Novel classes of histone deacetylase inhibitors(2006)29 cited
- → N3-Arylmalonamides: A new series of thieno[3,2-b]pyridine based inhibitors of c-Met and VEGFR2 tyrosine kinases(2009)27 cited
- → Design and synthesis of close analogs of LCRF-0004, a potent and selective RON receptor tyrosine kinase inhibitor(2015)20 cited
- → Synthesis of 5‐/10‐Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)‐Mediated Ring‐Closure Reaction(1996)20 cited