Dendrimeric ,-dipeptidic conjugates as organocatalysts in the asymmetric Michael addition reaction of isobutyraldehyde to N-phenylmaleimides

摘要

A series of polyester dendrimers (1G to 3G generation) based on 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoic acid (bis-MPA) and the core of 1,3-propanediol-2-(hydroxymethyl)-2-methyl (TME) were synthesized and conjugated to the ,-dipeptide (N-Cbz-Phe-N-Bn--Ala-COOH) in convergent fashion. Conventional esterification (DCC, DMAP, DPTS) was used for the above coupling, followed by removal of protecting groups (acetonide and Cbz groups) to provide seven novel organocatalysts exhibiting different sizes and solubilities. The dendritic nature (mono- or di-substituted), ending groups (acetonide or hydroxyl groups) and generation effects of these organocatalysts were evaluated in the Michael addition reaction of isobutyraldehyde to N-phenylmaleimide as benchmark reaction, both in solution and under neat reaction conditions. Reaction yields when using 10mol% of organocatalyst and NaOH as base varied in the range of good to excellent (neat 96%, aqueous solution 98%, CH2Cl2 solvent 80%), while enantioselectivity as high as 81:19 was achieved. The above enantioselectivity is in line with a positive dendritic effect. Regarding the influence of terminal groups, it is appreciated that hydroxyl end-groups afford higher yield relative to analogous acetonide terminal groups. Finally, the scope of the reaction was evaluated with catalysts H2N-Phe-N-Bn--Ala-TME-d-2G-A and H2N-Phe-N-Bn--Ala-TME-d-2G-OH, which could be recovered and recycled for at least three times without significant loss of catalytic activity.