F. Denonne

发表

Histamine H3 receptor ligands with a 3-cyclobutoxy motif: a novel and versatile constraint of the classical 3-propoxy linker

R. Leurs, H. Timmerman, I. D. Esch, 2010 .

Phenyl‐oxazoles, a New Family of Inverse Agonists at the H3 Histamine Receptor

Y. Lamberty, M. Gillard, B. Christophe, 2010, ChemMedChem.

Discovery of a New Class of Non‐imidazole Oxazoline‐Based Histamine H3 Receptor (H3R) Inverse Agonists

R. Leurs, H. Timmerman, Y. Lamberty, 2009, ChemMedChem.

Discovery of new C3aR ligands. Part 1: arginine derivatives.

T. Lewis, P. Pasau, P. Collart, 2007, Bioorganic & medicinal chemistry letters.

A GENERAL SYNTHESIS OF 2-FORMYL-3-ARYLPYRROLES

F. Denonne, L. Ghosez, Cécile Franc, 1999 .

Studies of palladium-catalyzed coupling reactions for preparation of hindered 3-arylpyrroles relevant to (-)-rhazinilam and its analogues

F. Denonne, L. Ghosez, R. Touillaux, 2001 .

Lead Optimization of Thiazolo[5,4‐c]piperidines: 3‐Cyclobutoxy Linker as a Key Spacer for H3R Inverse Agonists

Y. Lamberty, M. Gillard, B. Christophe, 2012, ChemMedChem.

Discovery of new C3aR ligands. Part 2: amino-piperidine derivatives.

P. Pasau, P. Collart, J. Nicolas, 2007, Bioorganic & medicinal chemistry letters.

8-Substituted 1,3-dimethyltetrahydropyrazino[2,1-f]purinediones: Water-soluble adenosine receptor antagonists and monoamine oxidase B inhibitors.

C. Müller, P. Koch, J. Heer, 2016, Bioorganic & medicinal chemistry.

Phenyl‐oxazoles, a New Family of Inverse Agonists at the H3 Histamine Receptor

Y. Lamberty, M. Gillard, B. Christophe, 2010, ChemMedChem.

Discovery of a New Class of Non‐imidazole Oxazoline‐Based Histamine H3 Receptor (H3R) Inverse Agonists

R. Leurs, H. Timmerman, Y. Lamberty, 2009, ChemMedChem.