Stereoselective Synthesis of Tetrasubstituted Alkenes via a Cp*Co^III‐Catalyzed C−H Alkenylation/Directing Group Migration Sequence

Abstract

Abstract A highly atom economical and stereoselective synthesis of tetrasubstituted α,β‐unsaturated amides was achieved by a Cp*Co III ‐catalyzed C−H alkenylation/directing group migration sequence. A carbamoyl directing group, which is typically removed after C−H functionalization, worked as an internal acylating agent and migrated onto the alkene moiety of the product. The directing group migration was realized with the Cp*Co III catalyst, while a related Cp*Rh III catalyst did not promote the migration process. The product was further converted into two types of tricyclic compounds, one of which had fluorescent properties.