Stéphane Raeppel - Concepedia

Author

Stéphane Raeppel

Pyrogenesis (Canada)

Also Known As

S. RAEPPEL, S. Raeppel, Stephane Raeppel, Stéphane L. Raeppel, Stéphane Raeppel

Publications

635

Citations

H-Index

Concepts

All Affiliations

Pyrogenesis (Canada)University of Toronto Centre National de la Recherche Scientifique RF Laboratories (United States)

About

Stéphane Raeppel is an author at Pyrogenesis (Canada) specializing in pharmacology, medicinal chemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	12	14	434
2	Medicine	11	13	386
3	Biochemistry	11	12	358
4	Engineering	4	4	154
5	Biomolecular Engineering	3	3	57

Stéphane Raeppel

Publications

585

Citations

H-Index

Page 1

	Year	Citations
Discovery of <i>N</i>-(2-Aminophenyl)-4-[(4-pyridin-3-ylpyrimidin-2-ylamino)methyl]benzamide (MGCD0103), an Orally Active Histone Deacetylase Inhibitor Nancy Zhou, Oscar Moradei, Stéphane Raeppel, Journal of Medicinal Chemistry Compound 8Chemoprevention StrategyPharmacotherapyInduces HistoneChemical Biology	2008	108
Lewis acid-catalyzed Mannich type reactions with potassium organotrifluoroborates Jean‐Philipe Tremblay‐Morin, Stéphane Raeppel, Frédéric Gaudette Tetrahedron Letters Cross-coupling ReactionEngineeringPotassium OrganotrifluoroboratesOrganic ChemistryOrganometallic Catalysis	2004	58
Amphoteric Character of 2-Vinyloxiranes: Synthetic Equivalents ofβ,γ-Unsaturated Aldehydes and a Vinylogous Enolate Mark Lautens, Stéphane G. Ouellet, Stéphane Raeppel Angewandte Chemie International Edition Interesting AlternativeEngineeringNatural SciencesSynthetic EquivalentsDiversity-oriented Synthesis	2000	56
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 Michael R. Mannion, Stéphane Raeppel, Stephen Claridge, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryDrug TargetNovel SeriesBiochemistryMedicine	2009	50
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 Isabelle Paquin, Stéphane Raeppel, Silvana Leit, Bioorganic & Medicinal Chemistry Letters Combinatorial ChemistryMedicinal ChemistryBioorganic ChemistryBiochemistryNatural Sciences	2007	35
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 Stéphane Raeppel, Stephen Claridge, Oscar Saavedra, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryDrug TargetNovel SeriesBiochemistryMedicine	2009	34
Substituted N-(2-aminophenyl)-benzamides, (E)-N-(2-aminophenyl)-acrylamides and their analogues: Novel classes of histone deacetylase inhibitors Oscar Moradei, Silvana Leit, Nancy Zhou, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryDerivative (Chemistry)Bioorganic ChemistryBiochemistryNatural Sciences	2006	29
N3-Arylmalonamides: A new series of thieno[3,2-b]pyridine based inhibitors of c-Met and VEGFR2 tyrosine kinases Oscar Saavedra, Stephen Claridge, Lijie Zhan, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryVegfr2 Tyrosine KinasesMedicineRational Drug DesignPharmacological Agent	2009	27
Synthesis of 5‐/10‐Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)‐Mediated Ring‐Closure Reaction Jean Suffert, Estelle Abraham, Stéphane Raeppel, Liebigs Annalen Medicinal ChemistryNeocarzinostatine ChromophoreEngineeringNew Dienediynes 5Phenanthrenes 23A	1996	20
Design and synthesis of close analogs of LCRF-0004, a potent and selective RON receptor tyrosine kinase inhibitor Stéphane Raeppel, Franck Raeppel, Éric Therrien Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryDrug TargetClose AnalogsBiochemistryMedicine	2015	20

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