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Jean-Francois CUPIF

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Jean-Francois CUPIF

UR1 - Chemistry Technician.

Université de Rennes 1
Faculté des Sciences Pharmaceutiques et Biologiques
Pharmacie : Institut des sciences chimiques de Rennes - UMR 6226
2 - AVE du Pr. Léon Bernard - CS 34317 - 35043 - RENNES CEDEX

Building 05-East, Office 00- 033
Phone: +33 (0) 2.23.23.48.91
Email: jean-francois.cupif@univ-rennes1.fr

Technical tasks / Responsabilities

• Organic synthesis.
• Set up and conduct chemical experiments, tests and analyses, using techniques such as chromatography, spectroscopy, physical and chemical separation techniques.
• “Chimiothèque Nationale” (CN) - French National Chemical Library – correspondent.

Scientific Production

11 Publications.

Dissymmetric Molecular Tweezers in Host-Guest Complexes: Internal or External Complexation?
T. Jaunet-Lahary, D.Jacquemin, B. Legouin, J-Y. Le Questel, J-F.Cupif, L. Toupet, P.Uriac, J. Graton, Journal of Physical Chemistry C (2015), 119(7), 3771-3779, DOI:10.1021/jp511418d

Synthesis of 1-arylidene-2,3-dihydro-1H-inden-2-ols through a tandem carbopalladation/Suzuki-Miyaura sequence.
E. Marchal, J-F. Cupif, P. Uriac, P. van de Weghe, Tetrahedron Letters (2008), 49(23), 3713-3715, 10.1016/j.tetlet.2008.04.042

Solid-phase synthesis and evaluation of libraries of substituted 4,5-dihydropyridazinones as vasodilator agents.
N. Gouault, C. Martin-Chouly, C. Lugnier, J-F. Cupif, A. Tonnelier, F. Feger, V. Lagente, M. David, Journal of Pharmacy and Pharmacology, 2004, Vol.56, Iss.8,1029-1037, DOI:10.1211/0022357043905

Synthesis and potential anti-inflammatory activity of some tetrahydrophthalazinones
N. Gouault , B. Pinel , J-F. Cupif, A. Depince , C. Martin-Chouly, C.Belleguic , M.David, Journal of enzyme inhibition and medicinal chemistry, 2004, Vol.19, Iss.6, 475-80, ISSN:1475-6366

Expedient method for the solid-phase synthesis of some 4-substituted-4,5-dihydropyridazin-3(2H)-ones.
N. Gouault, J-F. Cupif, M. Amoros, M. David, Journal of the Chemical Society, Perkin Transactions 1, 2002, Iss.20, 2234-2236, DOI:10.1039/b205607k