Organocatalytic asymmetric remote aziridination of 2,4-dienals

Kim Søholm Halskov, Tricia Naicker, Magnus E. Jensen, Karl Anker Jørgensen

Chemical Communications · 2013 · 77 citations · 51 references

Concepts

Abstract

Highly regio- and stereoselective remote aziridination of 2,4-dienals has been developed, based on a vinylogous iminium-ion-dienamine catalytic cascade reaction. Transformations of the aziridine products into enantioenriched motifs are also demonstrated. Furthermore, the reaction concept is extended to include enantioselective 1,6-addition of thiols.

References

51