J. Cupif

发表

Solid‐phase synthesis and evaluation of libraries of substituted 4,5‐dihydropyridazinones as vasodilator agents

V. Lagente, C. Martin-Chouly, C. Lugnier, 2004, The Journal of pharmacy and pharmacology.

Synthesis and Potential Anti-Inflammatory Activity of Some Tetrahydrophthalazinones

C. Martin-Chouly, A. Depincé, C. Belleguic, 2004, Journal of enzyme inhibition and medicinal chemistry.

Expedient method for the solid-phase synthesis of some 4-substituted-4,5-dihydropyridazin-3(2H)-ones

N. Gouault, M. David, M. Amorós, 2002 .

γ-Methyl-substituted-γ-butyrolactones: solid-phase synthesis employing a cyclisation–cleavage strategy

N. Gouault, M. David, J. Cupif, 2000 .

Synthesis of 1-arylidene-2,3-dihydro-1H-inden-2-ols through a tandem carbopalladation/Suzuki-Miyaura sequence

P. Uriac, P. D. Weghe, Estelle Marchal, 2008 .

Molecular Tweezers: Synthesis and Formation of Host–Guest Complexes

P. Uriac, P. D. Weghe, N. Levoin, 2010 .

Dissymmetric Molecular Tweezers in Host–Guest Complexes: Internal or External Complexation?

P. Uriac, D. Jacquemin, L. Toupet, 2015 .

Designed mono- and di-covalent inhibitors trap modeled functional motions for Trypanosoma cruzi proline racemase in crystallography

F. Saul, A. Blondel, P. Minoprio, 2018, PLoS neglected tropical diseases.

Alkylation of N,N-Dibenzylaminoacetonitrile: From Five- to Seven-Membered Nitrogen-Containing Heterocyclic Systems.

J. Hurvois, J. Renault, C. Bouvry, 2023, The Journal of organic chemistry.

Synthesis of diverse 4,5‐dihydro‐3(2H)‐pyridazinones on Wang resin

S. Picard, N. Gouault, M. David, 2001, The Journal of pharmacy and pharmacology.

Prodrugs as new therapies against Chagas disease: In vivo synergy between Trypanosoma cruzi proline racemase inhibitors and benznidazole: TcPRAC inhibitor prodrugs against Chagas disease.

A. Blondel, P. Minoprio, P. Uriac, 2021, Journal of Global Antimicrobial Resistance.