Abstract
AbstractThe reversibly formed CN bond plays a very important role in dynamic covalent chemistry and the CN/CN exchange of components between different imine constituents to create dynamic covalent libraries has been extensively used. To facilitate diversity generation, we have investigated an organocatalyzed approach, using L‐proline as catalyst, to accelerate the formation of dynamic libraries of [n×n] imine components. The organocatalysis methodology has also been extended, under somewhat modified conditions, to reversible CC/CN exchange processes between Knoevenagel derivatives of barbituric acid and imines, allowing for the generation of increased diversity.
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