‡ Both authors contributed equally to this study.
Abstract
In this feature article, a general perspective of the research program aimed towards
the preparation of polycyclic heterocycles by the means of enantioselective organocatalytic
multicomponent reactions is presented. Guidelines for reaction design, including the
selection of substrates and organocatalysts are discussed. For all transformations,
scope and limitations are presented, along with post-functionalization to afford diversified
heterocyclic scaffolds.
1 Introduction
2 Type I Products: 1,4,5,6-Tetrahydropyridines
3 Type II Products: 1,2,3,4-Tetrahydropyridines
4 Type III Products: Bridged Perhydropyridines
5 Conclusion and Perspective
Key words
1,3-dicarbonyls - enantioselectivity - heterocycles - Michael addition - multicomponent
reactions - organocatalysis