Decarboxylative Amination of SMAHOs by Dialkyl Azodicarboxylates

Abstract

The decarboxylative addition of substituted malonic acid half oxyesters (SMAHOs) to dialkyl azodicarboxylates is described. The reaction was promoted by 1,4‐diazabicyclo[2.2.2]octane (DABCO) as an organocatalyst in heated toluene. High yields of the coupling products were generally obtained, and the scope of the reaction proved rather important with the potential presence of functionalized pending chains at the α‐position, affording an original access to α‐aminoester derivatives.