Mariliis Kimm

Asymmetric catalysis plays one of the most important roles in the modern organic chemistry providing methods for the synthesis biologically active compounds and pharmaceuticals. Merging well-developed organocatalysis with electrochemistry opens new horizons for asymmetric transformation beyond the classical thermochemical activation. This approach is sustainable, since it employs harmless organocatalysts to induce chirality and electrons as traceless and green reagents to generate highly reactive radical species under mild reaction conditions avoiding the utilization of highly toxic and expensive RedOx chemicals. The efficiency and reliability of such transformations can be enhanced by performing the reaction in continuous-flow mode. The project is an example of cutting-edge science combining different research areas of organic synthesis and chemical engineering that can be potentially applied for discovery of new and potent life-saving drugs.

The project deals with the development of sustainable methods of asymmetric catalysis and their application in the synthesis of biologically relevant compounds. Various methods of catalysis (organo-, metal- and enzymatic catalysis) will be used separately or in cooperative manner. Special attention will be turned to the increase of efficiency of reactions by using selective catalysts, cascade or one-pot reactions. As a new method, a halogen bond donor catalyzed asymmetric reactions will be studied. New reactions will be applied on the synthesis of biologically active compounds and their derivatives. As a result, new asymmetric catalytic sustainable methods for the creating molecular complexity will be developed. Principles of green chemistry will take root in science, in the mode of thinking of PhD students and by PhD graduates in Estonian chemistry enterprises.