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.
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 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.