The progress of mankind is due exclusively to the progress of natural sciences, not to morals, religion or philosophy.
Justus von Liebig, 1866
INVITED LECTURES
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Domino Reactions. Concepts for Efficient Organic Synthesis -
Synthesis of Mucin Glycopeptide Antigens for the Development of Antitumor Vaccines -
Organic and organometallic tectones for supramolecular gels -
Transition Metal-Catalyzed Allylic Alkylations – Versatile Tools for Amino Acid and Peptide Syntheses -
Synthesis of Carbocycles and Heterocycles via Cascade Reactions of Morita-Baylis-Hillman Adducts of Nitroalkenes -
Chemoselective Nucleophilic Addition to N-Alkoxyamides: Development and Application to the Total Synthesis of Gephyrotoxin -
D-galactal as a source of readily available benzopyrans, chromenes and chromans -
Riding the beast with a Smiles: a journey along isocyanide-based multicomponent reactions -
The three-center-four electron halogen bond -
Synthesis of novel peptides through multicomponent reactions and investigation of their biological activities -
The Tale of Two Enantiomers - Organic Synthesis of Inhibitors of Enzymes and Protein-Protein-Interactions -
Palladium-Catalyzed Cyclization of Propargylic Esters with Nucleophiles -
Novel Molecular Photosensitizers for Dye-Sensitized Solar Cells and Photodynamic Therapy Applications
| OUR HISTORY |
| OCS-2009 | GEOHET-2011 |
Prof. Uli Kazmaier
Institut für Organische Chemie
Universität des Saarlandes
Im Stadtwald, Geb. C4.2
D-66123 Saarbrücken, Germany
Phone: +49 +681 302-3409
Fax: +49 +681 302-2409
e-Mail: u.kazmaier@mx.uni-saarland.de
Uli Kazmaier, born in 1960, studied chemistry at the University of Stuttgart where he obtained his diploma (1985) and his PhD (1989).
Afterwards he joined as a postdoc the research groups of M.T. Reetz (Marburg) and B.M. Trost (Stanford).
In 1992, he moved to Heidelberg starting his own scientific work as an habilitand at the Institute of Organic Chemistry. After his habilitation in 1997 he was privatdozent at the same University, and from 1999-2001 a substitute of a chair in Karlsruhe.
In 2000 he received a Novartis Chemistry Lectureship and a offer of a full professorship at the University Bayreuth. In 2001 he also obtained a offer of a full professorship at the University des Saarlandes, which he accepted in 2001.
In 2006 he received a call for a chair at university of Heidelberg, which he declined.
His current research interest extends to new organometallic reagents and reactions especially for amino acid and peptide synthesis. Besides the development of new synthetic protocols, the application of these new reactions towards the synthesis of natural products and other pharmaceutical relevant structures plays a central role. He is member of the DFG-funded research group FOR 1406 “Exploiting the Potential of Natural Compounds“. He published more that 175 papers in international journals.
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