Enantioselective Diels-Alder reaction in the confined space of homochiral metal-organic frameworks

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Abstract

A novel homochiral porous metal-organic framework (MOF) has been synthesized using (R)-2,2′-dihydroxy-1,1′-binaphthyl-4,4′-dibenzoic acid as the chiral ligand. This MOF acts as an effective heterogeneous catalyst for the enantioselective Diels-Alder reaction between isoprene and N-ethyl maleimide.

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Tanaka, K., Nagase, S., Anami, T., Wierzbicki, M., & Urbanczyk-Lipkowska, Z. (2016). Enantioselective Diels-Alder reaction in the confined space of homochiral metal-organic frameworks. RSC Advances, 6(112), 111436–111439. https://doi.org/10.1039/c6ra23740a

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