Abstract
Reactive imidazole intermediates based on AB2 and A3 monomers, i.e. bis(methylol) propionic acid (bis-MPA) and trimethylolpropane (TMP) have successfully been synthesized and isolated on a 100 gram scale via a facile synthetic protocol using 1,1′-carbonyldiimidazole (CDI) as a key reagent. The robustness of the imidazole intermediates as bench stable precursors enabled the synthesis of a library of functional cyclic carbonates bearing relevant functionalities including hydrophilic PEGs, bioactive cholesterol and clickable groups. A number of functional polycarbonates were obtained by ring-opening polymerization, and their relevance in biomedical applications was highlighted by their low cytotoxicity on human dermal fibroblasts (hDF).
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CITATION STYLE
Olsson, J. V., Hult, D., Cai, Y., García-Gallego, S., & Malkoch, M. (2014). Reactive imidazole intermediates: Simplified synthetic approach to functional aliphatic cyclic carbonates. Polymer Chemistry, 5(23), 6651–6655. https://doi.org/10.1039/c4py00911h
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