Construction of Acyclic Vicinal All-Carbon Quaternary and Tertiary Carbon Stereocenters via a Stereoselective Claisen Rearrangement

The selective construction of neighboring congested stereocenters in an acyclic setting bearing an all-carbon quaternary stereocenter is one of the important challenges in stereoselective synthesis. [3,3]-Sigmatropic rearrangements are powerful reactions with potential for the stereoselective construction of such arrays due to their intrinsic stereochemical nature associated with the well-defined and highly predictable transition state. However, such types of transformations are very difficult to catalyze in terms of selectivity and complexity. Herein, we outlined a diastereoselective Claisen rearrangement in the presence of a Cu^I catalyst and a tricoordinated ligand environment that enables complete stereocontrol, leading to chiral alcohols, amides, and oxazolines with vicinal all-carbon quaternary-tertiary or tertiary-tertiary stereodiads.