The aim is to engineer protoglobins for the efficient synthesis of n-alkylated α-aminoketones.
Engineering of enantiocomplementary protoglobins to facilitate chemical transformations.
Focus on stereoconvergent methods to enhance product versatility.
Successful transformation leading to a variety of pharmaceutically relevant α-aminoketones.
Enhanced efficiency in the construction process demonstrates the potential for broader applications.
Abstract
transformations, facilitating the conversion of simple chemicals into an array of valuable pharmaceutical compounds featuring aminoketone functionalities.