[Developments of highly stereoselective domino reactions and application to medicinal chemistry]

Simple and highly effective methods for the synthesis of polycyclic ring systems via two types of intramolecular domino reactions are developed and presented. The first example is an intramolecular double Michael reaction, whose scope-limitation, mechanism and application to natural product synthesis are discussed. The intramolecular Michael-aldol reaction is the second case, which provides a nice method for the preparation of polycyclic compounds having a four-membered ring system. In addition, some related reactions of these methods are described.