Vicinal stereocenters asymmetric allylic alkylation and Cope rearrangement: a straightforward route to functionally and stereochemically rich heterocycles

An asymmetric allylic alkylation/Cope rearrangement (AAA/[3,3]) capable of stereoselectively constructing vicinal stereocenters has been developed. Strategically integrated 4-methylation on the 3,3-dicyano-1,5-diene controls stereoselectivity and drives Cope rearrangement equilibrium in the forward direction. The AAA/[3,3] sequence rapidly converts abundant achiral and racemic starting materials into valuable (hetero)cycloalkane building blocks bearing significant functional and stereochemical complexity, highlighting the value of (hetero)cyclohexylidenemalononitriles as launching points for complex heterocycle synthesis. On this line, the resulting alkylidenemalononitrile moiety can be readily converted into amides via Hayashi-Lear amidation to ultimately yield amido-piperidines, tropanes, and related scaffolds with 3-5 stereocenters and drug-like functionality. Functionally and stereochemically rich saturated heterocycles are accessed stereoselectively from abundant resources. This work showcases the sequenced value of asymmetric allylic alkylation, Cope rearrangement, and Hayashi-Lear oxidative amidation.