R. Lavoie

发表

Development of potential antitumor agents. Synthesis and biological evaluation of a new set of sulfonamide derivatives as histone deacetylase inhibitors.

Daniel Delorme, A. Kalita, M. Robert, 2003, Journal of medicinal chemistry.

Indanylacetic acids as PPAR-δ activator insulin sensitizers

David P. Dickson, J. Livingston, T. Claus, 2007 .

Hepatitis C virus NS5A replication complex inhibitors: the discovery of daclatasvir.

L. Hamann, A. Fura, N. Meanwell, 2014, Journal of medicinal chemistry.

Design and synthesis of a novel class of histone deacetylase inhibitors.

S. Leit, S. Fréchette, G. Bouchain, 2001, Bioorganic & medicinal chemistry letters.

Derivatives of Mesoxalic Acid Block Translocation of HIV-1 Reverse Transcriptase*

D. Hazuda, A. Berghuis, S. Hecht, 2014, The Journal of Biological Chemistry.

N,N-Diethyl-4-[(3-hydroxyphenyl)(piperidin-4-yl)amino] benzamide derivatives: the development of diaryl amino piperidines as potent delta opioid receptor agonists with in vivo anti-nociceptive activity in rodent models.

D. Delorme, Paul B. Jones, E. Roberts, 2009, Bioorganic & Medicinal Chemistry Letters.

Constrained analogs of CB-1 antagonists: 1,5,6,7-Tetrahydro-4H-pyrrolo[3,2-c]pyridine-4-one derivatives.

Jennifer A. Natoli, Astrid A. Ortiz, B. Podlogar, 2007, Bioorganic & medicinal chemistry letters.

Asymmetric synthesis of diarylmethylamines: preparation of selective opioid delta receptor ligands

D. Delorme, E. Roberts, R. Lavoie, 1998 .

Transannular Diels–Alder Studies of 14-Membered cis–trans–trans Macrocyclic Trienes Having Allylic Ether or Enone Dienophile

S. Ouellet, Y. Dory, P. Deslongchamps, 2000 .

Synthesis of chiral trans-syn-cis and trans-anti-trans [6.6.6] tricycles by transannular Diels-Alder reaction

P. Deslongchamps, R. Lavoie, A. Toró, 1999 .

Optimization of imidazole amide derivatives as cannabinoid-1 receptor antagonists for the treatment of obesity.

Jennifer A. Natoli, Astrid A. Ortiz, S. O'connor, 2007, Bioorganic & medicinal chemistry letters.

Discovery of Benzodiazepine-Based Inhibitors of the E2 Enzyme UBCH10 from a Cell-Based p21 Degradation Screen.

T. Lorca, S. Meloche, L. Voisin, 2023, ACS chemical biology.