Non-Racemic Planar-Chiral Cyclophanes

  • Author: Veronika Belusa
  • Published Date: 08 July 2015
  • Source / Publisher: European Journal of Organic Chemistry/Wiley-VCH
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
thumbnail image: Non-Racemic Planar-Chiral Cyclophanes

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Cyclophanes are representative frameworks for planar chirality. Synthetic planar chiral cyclophanes are, for example, [2.2]paracyclophane derivatives (pictured). They are of great interest as asymmetric catalysts, and in medicinal and polymer chemistry. Producing non-racemic planar-chiral [2.2]paracyclophanes in a catalytic manner is still a challenge.

Kazuaki Kudo and colleagues, University of Tokyo, Japan, have developed a resin-supported peptide catalyst for kinetic resolution of a planar-chiral [2.2]paracyclophane derivative. This was done by a Michael addition of nitromethane to an enone substituent on the paracyclophane structure.

The resin-supported catalyst consists of a repetitive 310-helical unit, the amino acid sequence Leu-Leu-Aib, and two N-terminal tryptophan residues. The helical part of the peptide plays a critical role for the kinetic resolution. By optimizing the peptide sequence at the N-terminus of the helical chain, highly enantioselective resolution was obtained.


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