Dr. Cédric Kalinski
Senior Research Scientist

Cédric Kalinski was born 1979 in Macon (France), and studied chemistry at the Grande Ecole CPE Lyon (Ecole Supérieure de Chimie Physique Electronique de Lyon). He specialized in organic chemistry and joined Priaton 2002 as a trainee. He finished his Master degree in 2004 with a work about the MCR-synthesis of new building blocks for the pharmaceutical industry. Afterwards he achieved 2006 his PhD under the direction of Pr. Dr. Thorsten Bach at the Technical University of Munich and Priaton. The PhD-thesis describes new ways of synthesis of medicinally relevant heterocycles based on MCR-products modified by post-condensations. Since October 2006 he works as a Senior Research Scientist at Priaton with emphasis on the MCR-synthesis of new bioactive molecules. Furthermore he is responsible for the HPLC-purification department of the company and partially in charge of the business development.

 

List of publications

PhD-thesis: “New Combinations of Multicomponent reactions with classical post-condensations” 2006

Kalinski, C.; Umkehrer, M.; Schmidt, J.; Ross, G.; Kolb, J.; Burdack, C; Hiller, W.; Hoffmann, S.: A novel one-pot synthesis of highly diverse indole scaffolds by the Ugi/Heck reaction. Tetrahedron Lett. 2006, 47, 4683.

Kalinski, C.; Umkehrer, M.; Ross, G.; Kolb, J.; Burdack, C; Hiller, W.: Highly substituted indol-2-ones, quinoxalin-2-ones and benzodiazepin-2,5-diones via a new Ugi(4CR)-Pd assisted N-aryl amidation strategy. Tetrahedron Lett. 2006, 47, 3423.

Umkehrer, M.; Kalinski, C.; Kolb, J.; Burdack, C.: A new and versatile one-pot synthesis of indol-2-ones by a novel Ugi-four-component-Heck reaction. Tetrahedron Lett. 2006, 47, 2391.

Kalinski, C.; Umkehrer, M.; Gonnard, S.; Jäger, N.; Ross, G.; Hiller, W.: A new and versatile Ugi/SNAr synthesis of fused 4,5-dihydrotetrazolo[1,5-a]quinoxalines. Tetrahedron Lett. 2006, 47, 2041.

Mayer, J., Umkehrer, M., Kalinski, C., Ross, G., Kolb, J., Burdack C., Hiller, W.: New cleavable isocyanides for the combinatorial synthesis of a-amino acid analogue tetrazoles, Tetrahedron Lett 2005, 46, 7393.