Staff

Name Lagoutte Roman
Position Postdoctoral Fellow

Roman Lagoutte

Roman Lagoutte, Ph.D.

Postdoctoral Fellow



Institute of Organic Chemistry and Biochemistry ASCR, v.v.i.
Flemingovo nám. 2, CZ-166 10 Prague 6, Czech Republic

Phone: (+420) 220 183 451

 
Education
2007-2010 Ph.D., Centre for Biochemistry, Drug Design and Cancer Research, University of Salford (UK).
Supervisors: Dr. J.A. Wilkinson and Prof. S. Ducki.
Thesis: "Heparin mimics as potential inhibitors of the complex HGF/SF-Met: design, synthesis & biological evaluation".
2006-2007 Ingénieur-chimiste, Graduate School of Chemistry and Chemical Engineering (ENSCCF), Clermond-Ferrand (France).
M.Sc. "Analytical Biosciences & Drug Design", School of Environment & Life Sciences, University of Salford (UK).
Dissertation: "Synthesis of novel simplified sarcodictyin derivatives".
2004-2006 Graduate School of Chemistry and Chemical Engineering (ENSCCF), Clermond-Ferrand (France).
 
Experience
2007-2010 Ph.D .research project, Centre for Biochemistry, Drug Design and Cancer Research, University of Salford (UK).
2008 (2 months) Ph.D. training, analytical techniques in molecular biology, Paterson Institute for Cancer Research, Manchester (UK). Supervisor: Dr. M. Lyon.
2007 (8 months) M.Sc. research project, Centre for Biochemistry, Drug Design and Cancer Research, University of Salford.
2006 (3 months) 2nd year placement, Faculty of Chemistry, University of Wroclaw (Poland): "Synthesis and characterisation of novel zirconium oxide-based solid support for palladium as heterogeneous catalyst for cross-coupling reactions". Supervisor: Prof. A. Trzeciak, Prof. J.J. Ziółkowski.
2006 (3 months) 1st year placement, Clos d'Aguzon, Saint Auban sur l'Ouveze (France): "Industrial scale extraction of clary sage concrete".
 
Research interests
  • Development of novel tandem reactions involving organometallic and radical methodologies
  • Total synthesis of natural products
  • Design of novel bioactive compounds
  •  
    Publications
    R. Lagoutte, J.A. Wilkinson:
    A novel one-step method for the reductive allylation of esters and the first total synthesis of (±)-erythrococcamide B.
    Tetrahedron Letters 51: 6942-6944, 2010.