A mild method for the replacement of a hydroxyl group by halogen: 2. unified procedure and stereochemical studies von Gati, Wafa, Munyemana, François, Colens, Alain, Srour, Aladdin, Dufour, Mathilde, Vardhan Reddy, K. Harsha, Téchy, Brigitte, Rosse, Gérard, Schweiger, Ed, Qiao, Qi, Ghosez, Léon

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Azaspirooctane-carboxylates as Novel Activators/Modulators of M4 for the Treatment of Alzheimer’s Disease and Parkinson’s Disease von Rosse, Gerard

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Novel Aminopyrazole Inhibitors of PDE11A for the Treatment of Alzheimer’s Disease and Other Types of Dementia von Rosse, Gerard

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Novel Pyrrolo-pyrazol-one Ligands of Alpha-Synuclein for Diagnosis of Parkinson’s Disease von Rosse, Gerard

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Novel Pyrazolopyridine Inhibitors of Monoacylglycerol Lipase for the Treatment of Neurodegenerative Diseases and Neuroinflammation von Rosse, Gerard

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Phenyl-quinoline-xxo-butyric Acid Inhibitors of Histone Lysine Demethylase for the Treatment of Cancer von Rosse, Gerard

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Pyrazolidine Carboxamide Analogs as Selective Agonists of the Cannabinoid 2 Receptor von Rosse, Gerard

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Spiro-naphthyridine Antagonists of the Melanocortin Receptor 4 for the Treatment of Cachexia Associated with Chronic Illness von Rosse, Gerard

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Amino-cyclohexane Carboxylic Acid Inhibitors of Arginase von Rosse, Gerard

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Substituted Imidazole Carboxamides as Novel Antibacterial Agents von Rosse, Gerard

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A Series of Pyrazole Analogs Binding to KRASG12C as Potential Cancer Treatment von Rosse, Gerard

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Novel Methyl-aza-quinazolines as Inhibitors of the RAS-SOS Interaction von Rosse, Gerard

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Novel Pyrazolyl-dihydroisoquinolines as Positive Allosteric Modulator of the Dopamine D1 Receptor von Rosse, Gerard

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Erratum to “A mild method for the replacement of a hydroxyl group by halogen: 2. unified procedure and stereochemical studies” Tetrahedron 76 (37) (11 September 2020) 131441 von Gati, Wafa, Munyemana, François, Colens, Alain, Srour, Aladdin, Dufour, Mathilde, Reddy, K. Harsha Vardhan, Téchy, Brigitte, Rosse, Gérard, Schweiger, Ed, Qiao, Qi, Ghosez, Léon

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Imidazoquinolines as Novel Inhibitors of LRRK2 Kinase Activity von Rosse, Gerard

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Diazaspirononane Inhibitors of O‑GlcNAc Hydrolase for the Treatment of Central Nervous System Diseases von Rosse, Gerard

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Novel Bis-heteroaryl Derivatives To Modulate Protein Aggregation for the Treatment of Neurodegenerative Diseases von Rosse, Gerard

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Indolinone Inhibitors of ENT1 for the Treatment of Schizophrenia von Rosse, Gerard

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Antibody–Drug Conjugates for the Treatment of Inflammation von Rosse, Gerard

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Quinazoline Carboxamides as Selective Antagonists of Adenosine 2A Receptor von Rosse, Gerard

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