Replication Data for: Electroorganocatalytic asymmetric Diels-Alder cycloaddition of hydroquinones with ,-unsaturated aldehydes

The concept of combination of asymmetric aminocatalysis with electrochemistry stays unexplored. Herein, we report electrochemically driven Diels-Alder cycloaddition reactions of substituted hydroquinones to a series of dienophilic partners activated by TMS-protected prolinol catalyst leading to optically active products with high yields and perfect enantiomeric ratios up to 99:1 e.r.