Michel Belley

Medicine · Health Sciences

26h-index2.7kcitations70works0.02yr avg
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Research Topics

Inflammatory mediators and NSAID effects(13), Asthma and respiratory diseases(12), Synthesis and Reactions of Organic Compounds(10), Asymmetric Synthesis and Catalysis(8), Chemical Synthesis and Analysis(6)

Publications70 total

En réponse à …. Larivée, S. (2016). Traité de pensée magique pour jeunes ados. Revue de psychoéducation, 45(1), 211-228
Revue de psychoéducation·2016· 3 citedOpen Access
Préface
Presses de l'Université du Québec eBooks·2011
The identification of 4,7-disubstituted naphthoic acid derivatives as UDP-competitive antagonists of P2Y14
Bioorganic & Medicinal Chemistry Letters·2011· 55 citedOpen Access
Synthesis and SAR of pyrimidine-based, non-nucleotide P2Y14 receptor antagonists
Bioorganic & Medicinal Chemistry Letters·2011· 34 citedOpen Access
Remote Electronic Control in the Regioselective Reduction of Succinimides: A Practical, Scalable Synthesis of EP4 Antagonist MF-310
The Journal of Organic Chemistry·2009· 15 cited
Discovery of [(3-bromo-7-cyano-2-naphthyl)(difluoro)methyl]phosphonic acid, a potent and orally active small molecule PTP1B inhibitor
Bioorganic & Medicinal Chemistry Letters·2008· 55 citedOpen Access
ChemInform Abstract: Synthesis and Reactivity of N‐Hydroxy‐2‐amino‐2‐arylindoles.
ChemInform·2008
ChemInform Abstract: A New General Synthesis of N‐Hydroxyindoles.
ChemInform·2008
Structure–activity relationships and pharmacokinetic parameters of quinoline acylsulfonamides as potent and selective antagonists of the EP4 receptor
Bioorganic & Medicinal Chemistry Letters·2008· 18 citedOpen Access
Synthesis and Reactivity of <i>N</i>-Hydroxy-2-Amino-3-Arylindoles
Synlett·2007· 20 cited
A New General Synthesis of <i>N</i>-Hydroxyindoles
Synlett·2007· 14 cited
Comparison between two classes of selective EP3 antagonists and their biological activities
Bioorganic & Medicinal Chemistry Letters·2006· 32 citedOpen Access
Synthesis and Reactivity of N‐Hydroxy‐2‐aminoindoles.
ChemInform·2006
Synthesis and reactivity of N-hydroxy-2-aminoindoles
Tetrahedron Letters·2005· 32 cited
Aromatic Ring‐Opening of 2‐Fluorobenzothiophenes by Alkyllithiums.
ChemInform·2005
Structure—Activity Relationship Studies on ortho‐Substituted Cinnamic Acids, a New Class of Selective EP<sub>3</sub> Antagonists.
ChemInform·2005
Comparison of the Antinociceptive Profiles of Gabapentin and 3-Methylgabapentin in Rat Models of Acute and Persistent Pain: Implications for Mechanism of Action
Journal of Pharmacology and Experimental Therapeutics·2005· 73 cited
Aromatic Ring-Opening of 2-Fluorobenzothiophenes by Alkyllithiums
Synlett·2005· 17 cited
Structure–activity relationship studies on ortho-substituted cinnamic acids, a new class of selective EP3 antagonists
Bioorganic & Medicinal Chemistry Letters·2004· 28 citedOpen Access
Discovery and Synthesis of a Potent, Selective and Orally Bioavailable EP4 Receptor Agonist
Heterocycles·2004· 53 citedOpen Access
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Frequent Co-authors

Kathleen M. Metters(16), Robert Zamboni(15), J. Y. GAUTHIER(11), Marc Labelle(10), C. S. McFarlane(10), Robert N. Young(10), Y. LEBLANC(9), Robert J. Gordon(9), Nicole Sawyer(8), Thomas R. Jones(8), P. Masson(8), Yves Gareau(7), Éric Champion(7), A. W. Ford‐Hutchinson(7), Daniel Guay(7), H. Piechuta(7), Danielle Denis(6), C. Rochette(6), Nathalie Ouimet(6), L. Charette(6)