Diastereoselective Claisen rearrangement achieves complete stereocontrol in chiral compounds, indicating potential in synthesis.
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 CuI 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.
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Pati et al. (2025) studied this question.
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