Synthesis and Applications of Cinchona Squaramide‐Modified Poly(Glycidyl Methacrylate) Microspheres as Recyclable Polymer‐Grafted Enantioselective Organocatalysts

This work presents the immobilization of cinchona squaramide organocatalysts on poly(glycidyl methacrylate) solid supports. Preparation of the well‐defined monodisperse polymer microspheres was facilitated by comprehensive parameter optimization. By exploiting the reactive epoxy groups of the polymer support, three amino‐functionalized cinchona derivatives were immobilized on this carrier. To explore the effect of the amino linker, these structurally varied precatalysts were synthesized by modifying the cinchona skeleton at different positions. The catalytic activities of the immobilized organocatalysts were tested in the Michael addition of pentane‐2,4‐dione and trans‐β‐nitrostyrene with excellent yields (up to 98 %) and enantioselectivities (up to 96 % ee). Finally, the catalysts were easily recovered five times by centrifugation without loss of activity. Squaramides on spheres: On poly(glycidyl methacrylate) (PGMA), a well‐defined monodisperse microspherical polymer, new cinchona squaramides were immobilized by using different linkers. Their catalytic activity was tested in the Michael addition of pentane‐2,4‐dione and trans‐β‐nitrostyrene with excellent yields (up to 98 %) and ee (up to 96 % ee). The catalysts were recovered by centrifugation five times without loss of their activity.